EP4547672A1 - Modulateurs de la traduction d'arnm de c-myc et leurs utilisations dans le traitement du cancer - Google Patents

Modulateurs de la traduction d'arnm de c-myc et leurs utilisations dans le traitement du cancer

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Publication number
EP4547672A1
EP4547672A1 EP23836030.9A EP23836030A EP4547672A1 EP 4547672 A1 EP4547672 A1 EP 4547672A1 EP 23836030 A EP23836030 A EP 23836030A EP 4547672 A1 EP4547672 A1 EP 4547672A1
Authority
EP
European Patent Office
Prior art keywords
substituted
unsubstituted
linear
branched
piperidine
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
EP23836030.9A
Other languages
German (de)
English (en)
Inventor
Aviad MANDABI
Boaz Inbal
Scott Alexander SADLER
Shuyu CHU
David William Sheppard
Jason Paul Tierney
Iris Alroy
Rina WASSERMANN
Yoni SHEINBERGER
Yaode Wang
Haitang LI
Lothar Willms
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Anima Biotech Inc
Original Assignee
Anima Biotech Inc
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Filing date
Publication date
Priority claimed from US17/856,998 external-priority patent/US20220370431A1/en
Application filed by Anima Biotech Inc filed Critical Anima Biotech Inc
Publication of EP4547672A1 publication Critical patent/EP4547672A1/fr
Pending legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains three hetero rings
    • C07D513/14—Ortho-condensed systems

Definitions

  • the present invention relates to novel c-MYC mRNA translation modulators, composition and methods of preparation thereof, and uses thereof in the treatment of cancer.
  • BACKGROUND OF THE INVENTION Cancer is the second most common cause of death in the United States, exceeded only by heart disease. In the United States, cancer accounts for 1 of every 4 deaths. The 5-year relative survival rate for all cancer patients diagnosed in 1996-2003 is 66%, up from 50% in 1975-1977 (Cancer Facts & Figures American Cancer Society: Atlanta, GA (2008)).
  • the rate of new cancer cases decreased by an average 0.6% per year among men between 2000 and 2009 and stayed the same for women. From 2000 through 2009, death rates from all cancers combined decreased on average 1.8% per year among men and 1.4% per year among women. This improvement in survival reflects progress in diagnosing at an earlier stage and improvements in treatment. Discovering highly effective anticancer agents with low toxicity is a primary goal of cancer research.
  • the Myc family includes three major members, the proto-oncogene c-Myc (cellular Myelocytomatosis, short Myc), as well as L-myc and N-myc. These three Myc homologs are involved in the early stages of carcinogenesis and metastatic spread in most human cancers.
  • Myc gene In most types of tumors Myc gene is not mutated or duplicated, but its mRNA and/or protein levels are increased, indicating that in cancer Myc overexpression is induced at the level of transcription, mRNA steady state levels and translation. Indeed, myc gene expression normally depends on growth factor signaling and both myc mRNA and Myc protein have very short half-lives (of 30 and 20 min respectively) [Dang, C. V. (2012). MYC on the path to cancer. Cell 149, 22–35]. In tumor cells however, the cellular levels of Myc become independent from such signaling and regulation, and the resulting exacerbated Myc function drives intracellular and extracellular transcription programs that allow tumors to grow and thrive.
  • Myc does not necessarily need to be overexpressed in order for a cancer to be highly dependent upon its activity.
  • a study from Soucek et al. shows that tumors that express c-Myc at endogenous levels exhibit tumor regression upon Myc inhibition via a genetically engineered system. Therefore, treatment with a Myc inhibitor is not necessarily limited to cancers that overexpress Myc.
  • Compounds according to this invention may also be used to regulate the translation of Myc mRNA, wherein the direct target for the compounds is a protein or RNA which regulate Myc mRNA translation, and as such any tumor which is Myc dependent will benefit from the therapeutic utility of these compounds.
  • MYC is an important anticancer target.
  • Deregulated Myc gene is found in a wide range of human hematological malignancies and solid tumors, especially in breast cancer, ovarian carcinoma, acute myeloid leukemia, chronic myelogenous leukemia, Hodgkin’s and Burkitt’s lymphoma, diffuse large Bcell lymphoma, prostate cancer, colon cancer, gastric cancer, primary central nervous system lymphoma, glioblastoma, medulloblastoma, melanoma, non- small cell lung carcinoma, germinal center-derived lymphomas, esophageal squamous cell carcinoma, osteosarcoma, bladder cancer, pancreatic cancer and lung adenocarcinoma.
  • MYC protein lacks structural regions amenable to therapeutic inhibition by small molecules and is considered an undruggable target [BioDrugs (2019) 33:539–553].
  • Designing and developing MYC modulators is challenging, primarily because the MYC protein has a disordered structure which lacks a pocket or groove that can act as a binding site for modulators. Interfering with the MYC transcription, blocking the protein–protein interaction (PPI) of MYC and its cofactors, and influencing on signaling pathways related to MYC were used in the past as potential modulatory targets, but failed to be developed as drug candidates.
  • PPI protein–protein interaction
  • Myc PPI inhibitors failed to show sufficinet efficacy in cell-based assays and animal models due to the requirement of high target occupancy to drive efficacy.
  • Modulators of signaling pathways upstream to myc for example mTOR modulators, failed due to lack of target specificity.
  • mTOR modulators failed due to lack of target specificity.
  • target c-Myc has remained elusive.
  • the absence of a clear ligand-binding domain establishes a daunting obstacle toward direct inhibition, which is a challenging feature shared among many compelling transcriptional targets in cancer.
  • alternative modalities that target Myc are required, as outlined herein, namely compounds which regulate Myc mRNA translation.
  • This invention provides a compound or its pharmaceutically acceptable salt, stereoisomer, tautomer, hydrate, N-oxide, reverse amide analog, prodrug, isotopic variants (e.g., deuterated analog), PROTAC, pharmaceutical product or any combination thereof, represented by the structure of formula I(j), I(n) and/or I(o), and by the structures listed in Table 1, as defined herein below.
  • the compound is a c-MYC mRNA translation modulator.
  • the compound is a c-MYC mRNA transcription regulator.
  • the compound is a c- MYC inhibitor.
  • the compound is any combination of a c-MYC mRNA translation modulator, c-MYC mRNA transcription regulator and c-MYC inhibitor.
  • This invention further provides a pharmaceutical composition comprising a compound or its pharmaceutically acceptable salt, stereoisomer, tautomer, hydrate, N-oxide, prodrug, isotopic variants (e.g., deuterated analog), PROTAC, pharmaceutical product or any combination thereof, represented by the structure of formula I(j), I(n) and/or I(o), and by the structures listed in Table 1, as defined herein below, and a pharmaceutically acceptable carrier.
  • This invention further provides a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting cancer in a subject, comprising administering a compound represented by the structure of formula I(j), I(n) and/or I(o), and by the structures listed in Table 1, as defined herein below, to a subject suffering from cancer under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit cancer in said subject.
  • This invention further provides a method for suppressing, reducing or inhibiting tumor growth in a subject, comprising administering a compound represented by the structure of formula I(j), I(n) and/or I(o), and by the structures listed in Table 1, as defined herein below, to a subject, under conditions effective to suppress, reduce or inhibit tumor growth in said subject.
  • the tumor is cancerous.
  • the subject suffers from cancer.
  • This invention further provides a method of modulating c-MYC mRNA translation in a cell, comprising contacting a compound represented by the structure of formula I(j), I(n) and/or I(o)and by the structures listed in Table 1, as defined herein below, with a cell, thereby modulating c-MYC mRNA translation in said cell.
  • This invention further provides a method of regulating c-MYC mRNA transcription in a cell, comprising contacting a compound represented by the structure of formula I(j), I(n) and/or I(o) and by the structures listed in Table 1, as defined herein below, with a cell, thereby regulating c-MYC mRNA transcription in said cell.
  • FIG. 1 demonstrates how Protein Synthesis Monitoring (PSM) specifically monitors c-Myc synthesis.
  • the assay system comprises human non-small cell lung carcinoma cell line A549, which is expressing high level of c-Myc.
  • Two tRNAs (di-tRNA) which decode one specific glutamine codon and one specific serine codon were transfected with control RNAi or an RNAi directed to c-Myc.
  • FIG. 1 depicts selective regulation of c-Myc translation.
  • the panel demonstrates metabolic labeling in A549 cells, treated with vehicle, general translation inhibitor cycloheximide or anti-c-Myc compound. Treatment with cycloheximide resulted in total inhibition of global protein synthesis, while treatment with tested compound showed no significant effect.
  • Figure 3 demonstrates that compounds act at the level of mRNA processing/stability.
  • A549 cells were exposed to vehicle, general transcription inhibitor actinomycin D or anti-c-Myc compound.
  • actinomycin D or anti-c-Myc compound.
  • significant decrease in c-Myc protein level was observed after treatment with either actinomycin D or tested compound.
  • Lower panel shows complete reduction in c-Myc mRNA level as well as transcription sites after treatment with actinomycin D. Treatment with tested compound although reduced c-Myc mRNA levels by 30% without affecting transcription sites.
  • Figure 4 demonstrates the efficacy of compounds according to this invention in A549 cells.
  • Figure 5 demonstrates the in vivo data measured for compound 332.
  • Compound 332 inhibited c-Myc-dependent tumor growth in-vivo. Relative tumor volumes of A549 xenografts in NMRI female nude mice after treatment with compound 3 mg/kg twice a week for 49 days.
  • this invention is directed to a compound represented by the structure of formula (I): wherein X 2 , X 3 , and X 4 , are each independently nitrogen or CH; X 5 , X 6 , X 7 , X 8 and X 9 are each independently nitrogen or carbon atoms; X 10 is N, CH, or C(R) (e.g., C(CH 2 )OH, C(CH 2 ) 2 OH, C(NH-CH 2 -cyclopropyl), C(CH 3 ), C(cyclopropyl), C(isopropoxy), C(COOH)); R 5 is H or C 1 -C 5 linear or branched alkyl (e.g.
  • R 6 is H, F, Cl, Br, I, OH, SH, R 8 -OH, R 8 -SH, -R 8 -O-R 10 (e.g., CH 2 -O-CH 3 , (CH 2 ) 2 -O-CH 3 (CH 2 ) 3 -O-CH 3 , (CH 2 ) 2 -O-CH(CH 3 ) 2 ), R 8 -S-R 10 (e.g., (CH 2 ) 3 -S-(CH 2 ) 2 CH 3 ), R 8 -NHC(O)-R 10 , -O-R 8 - R 10 , R 8 -(substituted or unsubstituted C 3 -C 8 cycloalkyl) (e.g., CH 2 -cyclopropyl, CH 2 -cyclobutanol, CH 2 - difluorocyclopropyl, CH 2 -methylcyclopropyl, CH 2 -dimethylamin
  • R is H, F, Cl, Br, I, OH, SH, alkoxy, NH(R 10 ), NH-CH 2 -cyclopropyl, N(R 10 )(R 11 ), CF 3 , CN, NO 2 , COOH, C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl, ethyl, CH 2 -OH, CH 2 -CH 2 -OH, CH 2 -CH 2 -O-CH 2 -CH 2 ),
  • each R 8 is independently [CH 2 ] p wherein p is between 1 and 10;
  • R 9 is [CH] q , [C] q wherein q is between 2 and 10;
  • R 10 and R 11 are each independently H, C 1 -C 5 substituted or unsubstituted linear or branched alkyl (e.g., methyl, ethyl, CH 2 -cyclopropyl, CH 2 -CH 2 -O-CH 3 ), C 1 -C 5 substituted or unsubstituted linear or branched
  • X 2 , X 3 , and X 4 are each independently nitrogen or CH; X 5 , X 6 , X 7 , X 8 and X 9 are each independently nitrogen or carbon atoms; X 10 is N, CH, or C(R) (e.g., C(CH 2 )OH, C(CH 2 ) 2 OH, C(NH-CH 2 -cyclopropyl), C(CH 3 ), C(cyclopropyl), C(isopropoxy), C(COOH)); R 5 is H or C 1 -C 5 linear or branched alkyl (e.g.
  • R 30 is H, R 20 , F, Cl, Br, I, OH, SH, alkoxy, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), CF 3 , CN, NO 2 , C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl, ethyl, CH 2 -CH 2 -O-CH 2 -CH 2 -O-CH 3 , CH 2 -O-CH 2 -CH 2
  • this invention is directed to a compound represented by the structure of formula I(b): wherein X 2 , X 3 , and X 4 , are each independently nitrogen or CH; X 5 , X 6 , X 7 , X 8 and X 9 are each independently nitrogen or carbon atoms; X 10 is N, CH, or C(R) (e.g., C(CH 2 )OH, C(CH 2 ) 2 OH, C(NH-CH 2 -cyclopropyl), C(CH 3 ), C(cyclopropyl), C(isopropoxy), C(COOH)); R 6 is F, Cl, Br, I, OH, SH, R 8 -OH, R 8 -SH, -R 8 -O-R 10 (e.g., CH 2 -O-CH 3 ), R 8 -S-R 10 (e.g., (CH 2 ) 3 - S-(CH 2 ) 2 CH 3 ), R 8 -
  • R is H, F, Cl, Br, I, OH, SH, alkoxy, NH(R 10 ), NH-CH 2 -cyclopropyl, N(R 10 )(R 11 ), CF 3 , CN, NO 2 , COOH, C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl, ethyl, CH 2 -OH, CH 2 -CH 2 -OH, CH 2 -CH 2 -O-CH 2 -CH 2 ),
  • each R 8 is independently [CH 2 ] p wherein p is between 1 and 10;
  • R 9 is [CH] q , [C] q wherein q is between 2 and 10;
  • R 10 and R 11 are each independently H, C 1 -C 5 substituted or unsubstituted linear or branched alkyl (e.g., methyl, ethyl, CH 2 -cyclopropyl, CH 2 -CH 2 -O-CH 3 ), C 1 -C 5 substituted or unsubstituted linear or branched
  • X 2 , X 3 , and X 4 are each independently nitrogen or CH; X 5 , X 6 , X 7 , X 8 and X 9 are each independently nitrogen or carbon atoms; X 10 is N, CH, or C(R) (e.g., C(CH 2 )OH, C(CH 2 ) 2 OH, C(NH-CH 2 -cyclopropyl), C(CH 3 ), C(cyclopropyl), C(isopropoxy), C(COOH)); R 5 is H or C 1 -C 5 linear or branched alkyl (e.g.
  • R is H, F, Cl, Br, I, OH, SH, alkoxy, NH(R 10 ), NH-CH 2 -cyclopropyl, N(R 10 )(R 11 ), CF 3 , CN, NO 2 , COOH, C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl, ethyl, CH 2 -OH, CH 2 -CH 2 -OH, CH 2 -CH 2 -O-CH 2 -CH 2 ),
  • each R 8 is independently [CH 2 ] p wherein p is between 1 and 10;
  • R 9 is [CH] q , [C] q wherein q is between 2 and 10;
  • R 10 and R 11 are each independently H, C 1 -C 5 substituted or unsubstituted linear or branched alkyl (e.g., methyl, ethyl, CH 2 -cyclopropyl, CH 2 -CH 2 -O-CH 3 ), C 1 -C 5 substituted or unsubstituted linear or branched
  • this invention is directed to a compound represented by the structure of formula I(d): wherein X 2 , X 3 , and X 4 , are each independently nitrogen or CH; X 5 , X 6 , X 7 , X 8 and X 9 are each independently nitrogen or carbon atoms; X 10 is N, CH, or C(R) (e.g., C(CH 2 )OH, C(CH 2 ) 2 OH, C(NH-CH 2 -cyclopropyl), C(CH 3 ), C(cyclopropyl), C(isopropoxy), C(COOH)); wherein at least one of X 2 , X 3 , X 4 , X 5 , X 6 , X 7 , X 8 , X 9 or X 10 is N; R 5 is H or C 1 -C 5 linear or branched alkyl (e.g.
  • R 6 is H, F, Cl, Br, I, OH, SH, R 8 -OH, R 8 -SH, -R 8 -O-R 10 (e.g., CH 2 -O-CH 3 , (CH 2 ) 2 -O-CH 3 (CH 2 ) 3 -O-CH 3 , (CH 2 ) 2 -O-CH(CH 3 ) 2 ), R 8 -S-R 10 (e.g., (CH 2 ) 3 -S-(CH 2 ) 2 CH 3 ), R 8 -NHC(O)-R 10 , -O-R 8 - R 10 , R 8 -(substituted or unsubstituted C 3 -C 8 cycloalkyl) (e.g., CH 2 -cyclopropyl, CH 2 -cyclobutanol, CH 2 - difluorocyclopropyl, CH 2 -methylcyclopropyl, CH 2 -dimethylamin
  • R is H, F, Cl, Br, I, OH, SH, alkoxy, NH(R 10 ), NH-CH 2 -cyclopropyl, N(R 10 )(R 11 ), CF 3 , CN, NO 2 , COOH, C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl, ethyl, CH 2 -OH, CH 2 -CH 2 -OH, CH 2 -CH 2 -O-CH 2 -CH 2 ),
  • each R 8 is independently [CH 2 ] p wherein p is between 1 and 10;
  • R 9 is [CH] q , [C] q wherein q is between 2 and 10;
  • R 10 and R 11 are each independently H, C 1 -C 5 substituted or unsubstituted linear or branched alkyl (e.g., methyl, ethyl, CH 2 -cyclopropyl, CH 2 -CH 2 -O-CH 3 ), C 1 -C 5 substituted or unsubstituted linear or branched
  • this invention is directed to a compound represented by the structure of formula I(e): wherein X 2 , X 3 , and X 4 , are each independently nitrogen or CH; X 5 , X 6 , X 7 , X 8 and X 9 are each independently nitrogen or carbon atoms; X 10 is N, CH, or C(R) (e.g., C(CH 2 )OH, C(CH 2 ) 2 OH, C(NH-CH 2 -cyclopropyl), C(CH 3 ), C(cyclopropyl), C(isopropoxy), C(COOH)); R 6 and R 5 are joined to form a substituted or unsubstituted 5-8 membered heterocyclic ring (e.g., azepane, piperazine, 2-(piperazin-1-yl)acetamide); R 7 is H, F, Cl, Br, I, OH, O-R 20 , SH, R 8 -OH, R 8
  • R is H, F, Cl, Br, I, OH, SH, alkoxy, NH(R 10 ), NH-CH 2 -cyclopropyl, N(R 10 )(R 11 ), CF 3 , CN, NO 2 , COOH, C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl, ethyl, CH 2 -OH, CH 2 -CH 2 -OH, CH 2 -CH 2 -O-CH 2 -CH 2 ),
  • each R 8 is independently [CH 2 ] p wherein p is between 1 and 10;
  • R 9 is [CH] q , [C] q wherein q is between 2 and 10;
  • R 10 and R 11 are each independently H, C 1 -C 5 substituted or unsubstituted linear or branched alkyl (e.g., methyl, ethyl, CH 2 -cyclopropyl, CH 2 -CH 2 -O-CH 3 ), C 1 -C 5 substituted or unsubstituted linear or branched
  • this invention is directed to a compound represented by the structure of formula I(f): wherein A’ is a 3-8 membered single or fused, saturated, unsaturated or aromatic carbocyclic or heterocyclic ring (e.g., pyrrolidine, piperidine, piperazine, isochroman, 1,2,3,4-tetrahydroisoquinoline, indoline, isoindoline, 1,3-dihydroisobenzofuran, 2,3-dihydro-1H-indene, 1,2,3,4- tetrahydronaphthalene);
  • X 2 , X 3 , and X 4 are each independently nitrogen or CH;
  • X 10 is N, CH, or C(R) (e.g., C(CH 2 )OH, C(CH 2 ) 2 OH, C(NH-CH 2 -cyclopropyl), C(CH 3 ), C(cyclopropyl), C(isopropoxy), C(CO
  • R 6 is H, F, Cl, Br, I, OH, SH, R 8 -OH, R 8 -SH, -R 8 -O-R 10 (e.g., CH 2 -O-CH 3 , (CH 2 ) 2 -O-CH 3 (CH 2 ) 3 -O-CH 3 , (CH 2 ) 2 -O-CH(CH 3 ) 2 ), R 8 -S-R 10 (e.g., (CH 2 ) 3 -S-(CH 2 ) 2 CH 3 ), R 8 -NHC(O)-R 10 , -O-R 8 - R 10 , R 8 -(substituted or unsubstituted C 3 -C 8 cycloalkyl) (e.g., CH 2 -cyclopropyl, CH 2 -cyclobutanol, CH 2 - difluorocyclopropyl, CH 2 -methylcyclopropyl, CH 2 -dimethylamin
  • R is H, F, Cl, Br, I, OH, SH, alkoxy, NH(R 10 ), NH-CH 2 -cyclopropyl, N(R 10 )(R 11 ), CF 3 , CN, NO 2 , COOH, C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl, ethyl, CH 2 -OH, CH 2 -CH 2 -OH, CH 2 -CH 2 -O-CH 2 -CH 2 ),
  • each R 8 is independently [CH 2 ] p wherein p is between 1 and 10;
  • R 9 is [CH] q , [C] q wherein q is between 2 and 10;
  • R 10 and R 11 are each independently H, C 1 -C 5 substituted or unsubstituted linear or branched alkyl (e.g., methyl, ethyl, CH 2 -cyclopropyl, CH 2 -CH 2 -O-CH 3 ), C 1 -C 5 substituted or unsubstituted linear or branched
  • this invention is directed to a compound represented by the structure of formula I(g): wherein X 2 , X 3 , and X 4 , are each independently nitrogen or CH; X 5 , X 6 , X 7 , X 8 and X 9 are each independently nitrogen or carbon atoms; X 10 is N, CH, or C(R) (e.g., C(CH 2 )OH, C(CH 2 ) 2 OH, C(NH-CH 2 -cyclopropyl), C(CH 3 ), C(cyclopropyl), C(isopropoxy), C(COOH)); R 100 is a C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl, ethyl), R 8 - OH (e.g., (CH 2 ) 2 -OH), -R 8 -O-R 10 (e.g., (CH 2 ) 2 -O-
  • R 6 is H, F, Cl, Br, I, OH, SH, R 8 -OH, R 8 -SH, -R 8 -O-R 10 (e.g., CH 2 -O-CH 3 , (CH 2 ) 2 -O-CH 3 (CH 2 ) 3 -O-CH 3 , (CH 2 ) 2 -O-CH(CH 3 ) 2 ), R 8 -S-R 10 (e.g., (CH 2 ) 3 -S-(CH 2 ) 2 CH 3 ), R 8 -NHC(O)-R 10 , -O-R 8 - R 10 , R 8 -(substituted or unsubstituted C 3 -C 8 cycloalkyl) (e.g., CH 2 -cyclopropyl, CH 2 -cyclobutanol, CH 2 - difluorocyclopropyl, CH 2 -methylcyclopropyl, CH 2 -dimethylamin
  • R is H, F, Cl, Br, I, OH, SH, alkoxy, NH(R 10 ), NH-CH 2 -cyclopropyl, N(R 10 )(R 11 ), CF 3 , CN, NO 2 , COOH, C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl, ethyl, CH 2 -OH, CH 2 -CH 2 -OH, CH 2 -CH 2 -O-CH 2 -CH 2 ),
  • each R 8 is independently [CH 2 ] p wherein p is between 1 and 10;
  • R 9 is [CH] q , [C] q wherein q is between 2 and 10;
  • R 10 and R 11 are each independently H, C 1 -C 5 substituted or unsubstituted linear or branched alkyl (e.g., methyl, ethyl, CH 2 -cyclopropyl, CH 2 -CH 2 -O-CH 3 ), C 1 -C 5 substituted or unsubstituted linear or branched
  • R 100 is methyl and R 5 is H, then R 12 and R 13 are not both alkyls. In some embodiments, if R 100 is methyl and R 5 is H, then R 12 and R 13 cannot be joined to form piperidine.
  • this invention is directed to a compound represented by the structure of formula I(h): wherein X 2 , X 3 , and X 4 , are each independently nitrogen or CH; X 5 , X 6 , X 7 , X 8 and X 9 are each independently nitrogen or carbon atoms; X 10 is N, CH, or C(R) (e.g., C(CH 2 )OH, C(CH 2 ) 2 OH, C(NH-CH 2 -cyclopropyl), C(CH 3 ), C(cyclopropyl), C(isopropoxy), C(COOH)); Ring F is absent or is a substituted or unsubstituted, saturated or unsaturated, 4-8 membered heterocyclic ring (e.g., pyrrolidine, morpholine, 1-methylpyrrolidine, pyrrolidin-2-one, pyrrolidin-3- one, 3,3-difluoropyrrolidine, pyrrolidine-3-
  • R 6 is H, F, Cl, Br, I, OH, SH, R 8 -OH, R 8 -SH, -R 8 -O-R 10 (e.g., CH 2 -O-CH 3 , (CH 2 ) 2 -O-CH 3 (CH 2 ) 3 -O-CH 3 , (CH 2 ) 2 -O-CH(CH 3 ) 2 ), R 8 -S-R 10 (e.g., (CH 2 ) 3 -S-(CH 2 ) 2 CH 3 ), R 8 -NHC(O)-R 10 , -O-R 8 - R 10 , R 8 -(substituted or unsubstituted C 3 -C 8 cycloalkyl) (e.g., CH 2 -cyclopropyl, CH 2 -cyclobutanol, CH 2 - difluorocyclopropyl, CH 2 -methylcyclopropyl, CH 2 -dimethylamin
  • R 30 is H, R 20 , F, Cl, Br, I, OH, SH, alkoxy, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), CF 3 , CN, NO 2 , C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl, ethyl, CH 2 -CH 2 -O-CH 2 -CH 2 -O-CH 3 , CH 2 -O-CH 2 -CH 2
  • each R 8 is independently [CH 2 ] p wherein p is between 1 and 10;
  • R 9 is [CH] q , [C] q wherein q is between 2 and 10;
  • R 10 and R 11 are each independently H, C 1 -C 5 substituted or unsubstituted linear or branched alkyl (e.g., methyl, ethyl, CH 2 -cyclopropyl, CH 2 -CH 2 -O-CH 3 ), C 1 -C 5 substituted or unsubstituted linear or branched
  • this invention is directed to a compound represented by the structure of formula I(i): wherein X 2 , X 3 , and X 4 , are each independently nitrogen or CH; X 5 , X 6 , X 7 , X 8 and X 9 are each independently nitrogen or carbon atoms; X 10 is N, CH, or C(R) (e.g., C(CH 2 )OH, C(CH 2 ) 2 OH, C(NH-CH 2 -cyclopropyl), C(CH 3 ), C(cyclopropyl), C(isopropoxy), C(COOH)); R 5 is H or C 1 -C 5 linear or branched alkyl (e.g.
  • R 6 is H, F, Cl, Br, I, OH, SH, R 8 -OH, R 8 -SH, -R 8 -O-R 10 (e.g., CH 2 -O-CH 3 , (CH 2 ) 2 -O-CH 3 (CH 2 ) 3 -O-CH 3 , (CH 2 ) 2 -O-CH(CH 3 ) 2 ), R 8 -S-R 10 (e.g., (CH 2 ) 3 -S-(CH 2 ) 2 CH 3 ), R 8 -NHC(O)-R 10 , -O-R 8 - R 10 , R 8 -(substituted or unsubstituted C 3 -C 8 cycloalkyl) (e.g., CH 2 -cyclopropyl, CH 2 -cyclobutanol, CH 2 - difluorocyclopropyl, CH 2 -methylcyclopropyl, CH 2 -dimethylamin
  • R 30 is H, R 20 , F, Cl, Br, I, OH, SH, alkoxy, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), CF 3 , CN, NO 2 , C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl, ethyl, CH 2 -CH 2 -O-CH 2 -CH 2 -O-CH 3 , CH 2 -O-CH 2 -CH 2
  • each R 8 is independently [CH 2 ] p wherein p is between 1 and 10;
  • R 9 is [CH] q , [C] q wherein q is between 2 and 10;
  • R 10 and R 11 are each independently H, C 1 -C 5 substituted or unsubstituted linear or branched alkyl (e.g., methyl, ethyl, CH 2 -cyclopropyl, CH 2 -CH 2 -O-CH 3 ), C 1 -C 5 substituted or unsubstituted linear or branched
  • this invention is directed to a compound represented by the structure of formula I(j): wherein X 2 , X 3 , and X 4 , are each independently nitrogen or CH; X 10 is N, CH, or C(R) (e.g., C(CH 2 )OH, C(CH 2 ) 2 OH, C(NH-CH 2 -cyclopropyl), C(CH 3 ), C(cyclopropyl), C(isopropoxy), C(COOH)); Ring W is a 3-10 membered single, fused, bridged or spiro, saturated, unsaturated or aromatic, carbocyclic or heterocyclic ring (e.g., morpholine, tetrahydrofuran, tetrahydropyran, oxetane, oxetan-3- ol, pyrrolidine, pyrrolidin-2-ol, pyrrolidin-3-ol, 3-methoxypyrrolidine, 3-
  • R 30 is H, R 20 , F, Cl, Br, I, OH, SH, alkoxy, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), CF 3 , CN, NO 2 , C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl, ethyl, CH 2 -CH 2 -O-CH 2 -CH 2 -O-CH 3 , CH 2 -O-CH 2 -CH 2
  • R 200 is H, R 20 , F, Cl, Br, I, OH, SH, alkoxy, NH 2 , N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), CF 3 , CN, NO 2 , C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl, ethyl, CH 2 -CH 2 -O-CH 2 -CH 2 - O-CH 3 , CH 2 -O-CH 2
  • each R 8 is independently [CH 2 ] p wherein p is between 1 and 10;
  • R 9 is [CH] q , [C] q wherein q is between 2 and 10;
  • R 10 and R 11 are each independently H, C 1 -C 5 substituted or unsubstituted linear or branched alkyl (e.g., methyl, ethyl, CH 2 -cyclopropyl, CH 2 -CH 2 -O-CH
  • the compound is not (R)-2-(2-fluoro-4-(pyrrolidin-2-yl)phenyl)-N-(3- (4-fluoropiperidin-1-yl)propyl) benzo[d]imidazo [2,1-b] thiazole-7-carboxamide.
  • the compound is not (S)-2-(2-fluoro-4-(pyrrolidin-2-yl)phenyl)-N-(3-(4-fluoropiperidin- 1-yl)propyl)benzo[d]imidazo[2,1-b]thiazole-7-carboxamide.
  • the compound is not 2-(2-fluoro-4-(pyrrolidin-2-yl)phenyl)-N-(3-(4-fluoropiperidin-1-yl)propyl) benzo[d]imidazo[2,1- b]thiazole-7-carboxamide.
  • this invention is directed to a compound represented by the structure of formula I(k):
  • X 2 , X 3 , and X 4 are each independently nitrogen or CH;
  • X 10 is N, CH, or C(R) (e.g., C(CH 2 )OH, C(CH 2 ) 2 OH, C(NH-CH 2 -cyclopropyl), C(CH 3 ), C(cyclopropyl), C(isopropoxy), C(COOH));
  • Q 1 is O, NH or CH 2 ;
  • R 7 and R 7 ’ are each independently H, F, Cl, Br, I, OH, O-R 20 , SH, R 8 -OH, R 8 -SH, -R 8 -O-R 10 , R 8 -(C 3 -C 8 cycloalkyl), R 8 -(3-8 membered heterocyclic ring), CF 3 , CD 3 , OCD 3 , CN, NO 2 , -CH 2 CN, - R 8
  • R 200 is H, R 20 , F, Cl, Br, I, OH, SH, alkoxy, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), CF 3 , CN, NO 2 , C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl, ethyl, CH 2 -CH 2 -O-CH 2 -CH 2 -O-CH 3 , CH 2 -O-CH 2 -CH 2
  • each R 8 is independently [CH 2 ] p wherein p is between 1 and 10;
  • R 9 is [CH] q , [C] q wherein q is between 2 and 10;
  • R 10 and R 11 are each independently H, C 1 -C 5 substituted or unsubstituted linear or branched alkyl (e.g., methyl, ethyl, CH 2 -cyclopropyl, CH 2 -CH 2 -O-CH
  • the compound is not (R)-2-(2-fluoro-4-(pyrrolidin-2-yl)phenyl)-N-(3- (4-fluoropiperidin-1-yl)propyl) benzo[d]imidazo [2,1-b] thiazole-7-carboxamide.
  • the compound is not (S)-2-(2-fluoro-4-(pyrrolidin-2-yl)phenyl)-N-(3-(4-fluoropiperidin- 1-yl)propyl)benzo[d]imidazo[2,1-b]thiazole-7-carboxamide.
  • the compound is not 2-(2-fluoro-4-(pyrrolidin-2-yl)phenyl)-N-(3-(4-fluoropiperidin-1-yl)propyl) benzo[d]imidazo[2,1- b]thiazole-7-carboxamide.
  • this invention is directed to a compound represented by the structure of formula I(l): wherein X 2 , X 3 , and X 4 , are each independently nitrogen or CH; X 10 is N, CH, or C(R) (e.g., C(CH 2 )OH, C(CH 2 ) 2 OH, C(NH-CH 2 -cyclopropyl), C(CH 3 ), C(cyclopropyl), C(isopropoxy), C(COOH)); R 5 is H or C 1 -C 5 linear or branched alkyl (e.g.
  • R 6 is H, F, Cl, Br, I, OH, SH, R 8 -OH, R 8 -SH, -R 8 -O-R 10 (e.g., CH 2 -O-CH 3 , (CH 2 ) 2 -O-CH 3 (CH 2 ) 3 -O-CH 3 , (CH 2 ) 2 -O-CH(CH 3 ) 2 ), R 8 -S-R 10 (e.g., (CH 2 ) 3 -S-(CH 2 ) 2 CH 3 ), R 8 -NHC(O)-R 10 , -O-R 8 - R 10 , R 8 -(substituted or unsubstituted C 3 -C 8 cycloalkyl) (e.g., CH 2 -cyclopropyl, CH 2 -cyclobutanol, CH 2 - difluorocyclopropyl, CH 2 -methylcyclopropyl, CH 2 -dimethylamin
  • R 30 is H, R 20 , F, Cl, Br, I, OH, SH, alkoxy, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), CF 3 , CN, NO 2 , C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl, ethyl, CH 2 -CH 2 -O-CH 2 -CH 2 -O-CH 3 , CH 2 -O-CH 2 -CH 2
  • R 200 is H, R 20 , F, Cl, Br, I, OH, SH, alkoxy, NH 2 , N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), CF 3 , CN, NO 2 , C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl, ethyl, CH 2 -CH 2 -O-CH 2 -CH 2 - O-CH 3 , CH 2 -O-CH 2
  • each R 8 is independently [CH 2 ] p wherein p is between 1 and 10;
  • R 9 is [CH] q , [C] q wherein q is between 2 and 10;
  • R 10 and R 11 are each independently H, C 1 -C 5 substituted or unsubstituted linear or branched alkyl (e.g., methyl, ethyl, CH 2 -cyclopropyl, CH 2 -CH 2 -O-CH
  • R 6 of compound of formula I(l) is H, C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl), substituted or unsubstituted 3-8 membered heterocyclic ring (e.g., piperidine, 1-methylpiperidine, 3-fluoro-1-methylpiperidine, azetidine, 1-methyl-azetidine, morpholine, pyrrolidine, pyrrolidinone, quinuclidine, tetrahydropyran, tetrahydrofurane, azaspiro[3.3]heptane, 8-methyl-8-azabicyclo[3.2.1]octane, dioxane, 1,3-dioxane; each represents a separate embodiment according to this invention).
  • substituted or unsubstituted alkyl e.g., methyl
  • substituted or unsubstituted 3-8 membered heterocyclic ring e.
  • R 6 is H. . In various embodiments, R 6 is C 1 -C 5 linear or branched, substituted or unsubstituted alkyl. In various embodiments, R 6 is methyl. In various embodiments, R 6 is substituted or unsubstituted 3-8 membered heterocyclic ring. In various embodiments, R 6 is piperidine. In various embodiments, R 6 is 1- methylpiperidine. In various embodiments, R 6 is 3-fluoro-1-methylpiperidine. In various embodiments, R 6 is azetidine. In various embodiments, R 6 is 1-methyl-azetidine. In various embodiments, R 6 is morpholine. In various embodiments, R 6 is tetrahydropyran.
  • R 6 is tetrahydrofurane. In various embodiments, R 6 is 8-methyl-8-azabicyclo[3.2.1]octane. In various embodiments, R 6 is dioxane. In various embodiments, R 6 is 1,3-dioxane. [0037] In various embodiments, this invention is directed to a compound represented by the structure of formula I(m):
  • R 30 is H, R 20 , F, Cl, Br, I, OH, SH, alkoxy, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), CF 3 , CN, NO 2 , C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl, ethyl, CH 2 -CH 2 -O-CH 2 -CH 2 -O-CH 3 , CH 2 -O-CH 2 -CH 2
  • each R 8 is independently [CH 2 ] p wherein p is between 1 and 10;
  • R 9 is [CH] q , [C] q wherein q is between 2 and 10;
  • R 10 and R 11 are each independently H, C 1 -C 5 substituted or unsubstituted linear or branched alkyl (e.g., methyl, ethyl, CH 2 -cyclopropyl, CH 2 -CH 2 -O-CH 3 ), C 1 -C 5 substituted or unsubstituted linear or branched
  • this invention is directed to a compound represented by the structure of formula I(n): wherein X 2 , X 3 , and X 4 , are each independently nitrogen or CH; X 10 is N, CH, or C(R) (e.g., C(CH 2 )OH, C(CH 2 ) 2 OH, C(NH-CH 2 -cyclopropyl), C(CH 3 ), C(cyclopropyl), C(isopropoxy), C(COOH)); Ring W is a 3-10 membered single, fused, bridged or spiro, saturated, unsaturated or aromatic, carbocyclic or heterocyclic ring (e.g., morpholine, tetrahydrofuran, tetrahydropyran, oxetane, oxetan-3- ol, pyrrolidine, pyrrolidin-2-ol, pyrrolidin-3-ol, 3-methoxypyrrolidine, 3-
  • R 6 is H, F, Cl, Br, I, OH, SH, R 8 -OH, R 8 -SH, -R 8 -O-R 10 (e.g., CH 2 -O-CH 3 , (CH 2 ) 2 -O-CH 3 (CH 2 ) 3 -O-CH 3 , (CH 2 ) 2 -O-CH(CH 3 ) 2 ), R 8 -S-R 10 (e.g., (CH 2 ) 3 -S-(CH 2 ) 2 CH 3 ), R 8 -NHC(O)-R 10 , -O-R 8 - R 10 , R 8 -(substituted or unsubstituted C 3 -C 8 cycloalkyl) (e.g., CH 2 -cyclopropyl, CH 2 -cyclobutanol, CH 2 - difluorocyclopropyl, CH 2 -methylcyclopropyl, CH 2 -dimethylamin
  • R 30 is H, R 20 , F, Cl, Br, I, OH, SH, alkoxy, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), CF 3 , CN, NO 2 , C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl, ethyl, CH 2 -CH 2 -O-CH 2 -CH 2 -O-CH 3 , CH 2 -O-CH 2 -CH 2
  • R 200 is H, R 20 , F, Cl, Br, I, OH, SH, alkoxy, NH 2 , N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), CF 3 , CN, NO 2 , C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl, ethyl, CH 2 -CH 2 -O-CH 2 -CH 2 - O-CH 3 , CH 2 -O-CH 2
  • each R 8 is independently [CH 2 ] p wherein p is between 1 and 10;
  • R 9 is [CH] q , [C] q wherein q is between 2 and 10;
  • R 10 and R 11 are each independently H, C 1 -C 5 substituted or unsubstituted linear or branched alkyl (e.g., methyl, ethyl, CH 2 -cyclopropyl, CH 2 -CH 2 -O-CH
  • the compound is not (R)-2-(2-fluoro-4-(pyrrolidin-2-yl)phenyl)-N-(3- (4-fluoropiperidin-1-yl)propyl) benzo[d]imidazo [2,1-b] thiazole-7-carboxamide.
  • the compound is not (S)-2-(2-fluoro-4-(pyrrolidin-2-yl)phenyl)-N-(3-(4-fluoropiperidin- 1-yl)propyl)benzo[d]imidazo[2,1-b]thiazole-7-carboxamide.
  • the compound is not 2-(2-fluoro-4-(pyrrolidin-2-yl)phenyl)-N-(3-(4-fluoropiperidin-1-yl)propyl) benzo[d]imidazo[2,1- b]thiazole-7-carboxamide.
  • this invention is directed to a compound represented by the structure of formula I(o): wherein X 2 , X 3 , and X 4 are each independently nitrogen or CH; X 5 , X 6 , X 7 , X 8 and X 9 are each independently nitrogen or carbon atoms; X 10 is N, CH, or C(R) (e.g., C(CH 2 )OH, C(CH 2 ) 2 OH, C(NH-CH 2 -cyclopropyl), C(CH 3 ), C(cyclopropyl), C(isopropoxy), C(COOH)); R 1 is H, F, Cl, Br, I, OH, SH, or CF 3 , substituted or unsubstituted C 1 -C 5 alkyl (e.g., CH 2 OH), C 1 -C 5 linear or branched, or C 3 -C 8 cyclic haloalkyl, substituted or unsubstituted C 1 -C 5 alkyl (e
  • R 6 is H, F, Cl, Br, I, OH, SH, R 8 -OH, R 8 -SH, -R 8 -O-R 10 (e.g., CH 2 -O-CH 3 , (CH 2 ) 2 -O-CH 3 (CH 2 ) 3 -O-CH 3 , (CH 2 ) 2 -O-CH(CH 3 ) 2 ), R 8 -S-R 10 (e.g., (CH 2 ) 3 -S-(CH 2 ) 2 CH 3 ), R 8 -NHC(O)-R 10 , -O-R 8 - R 10 , R 8 -(substituted or unsubstituted C 3 -C 8 cycloalkyl) (e.g., CH 2 -cyclopropyl, CH 2 -cyclobutanol, CH 2 - difluorocyclopropyl, CH 2 -methylcyclopropyl, CH 2 -dimethylamin
  • R 30 is H, R 20 , F, Cl, Br, I, OH, SH, alkoxy, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), CF 3 , CN, NO 2 , C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl, ethyl, CH 2 -CH 2 -O-CH 2 -CH 2 -O-CH 3 , CH 2 -O-CH 2 -CH 2
  • each R 8 is independently [CH 2 ] p wherein p is between 1 and 10;
  • R 9 is [CH] q , [C] q wherein q is between 2 and 10;
  • R 10 and R 11 are each independently H, C 1 -C 5 substituted or unsubstituted linear or branched alkyl (e.g., methyl, ethyl, CH 2 -cyclopropyl, CH 2 -CH 2 -O-CH 3 ), C 1 -C 5 substituted or unsubstituted linear or branched
  • R 7 ' is F. In various embodiments, R 7 '' is H. In various embodiments, R 1 is H. In various embodiments, R 2 is a substituted C 1 -C 5 alkyl. In various embodiments, R 2 is CH 2 OH. In various embodiments, R 2 is CH 2 OCH 3 . In various embodiments, R 2 is 3-8 membered heterocyclic ring. In various embodiments, R 2 is oxetane. In various embodiments, R 2 is 3-oxetane or 2-oxetane; each represents a separate embodiment. In various embodiments, R 6 is H.
  • R 6 is C 1 -C 5 linear or branched, substituted or unsubstituted alkyl. In various embodiments, R 6 is methyl. In various embodiments, R 6 is substituted or unsubstituted, saturated or unsaturated, single fused, bridged or spiro 3-10 membered heterocyclic ring. In various embodiments, R 6 is substituted or unsubstituted, saturated single 3-8 membered heterocyclic ring. In various embodiments, the heterocyclic ring is tetrahydropyrane.
  • R 7 ' is F
  • R 1 is H and R 6 is unsubstituted C 1 -C 5 linear or branched, alkyl or substituted or unsubstituted, saturated single 3-8 membered heterocyclic ring.
  • R 7 ' is F
  • R 1 is H and R 6 is methyl.
  • this invention is directed to a compound represented by the structure of formula (II): wherein X 2 , X 3 , and X 4 , are each independently nitrogen or CH; X 5 , X 6 , X 7 , X 8 and X 9 are each independently nitrogen or carbon atoms; X 10 is N, CH, or C(R) (e.g., C(CH 2 )OH, C(CH 2 ) 2 OH, C(NH-CH 2 -cyclopropyl), C(CH 3 ), C(cyclopropyl), C(isopropoxy), C(COOH)); R 5 is H or C 1 -C 5 linear or branched alkyl (e.g.
  • R 6 is H, F, Cl, Br, I, OH, SH, R 8 -OH, R 8 -SH, -R 8 -O-R 10 (e.g., CH 2 -O-CH 3 , (CH 2 ) 2 -O-CH 3 (CH 2 ) 3 -O-CH 3 , (CH 2 ) 2 -O-CH(CH 3 ) 2 ), R 8 -S-R 10 (e.g., (CH 2 ) 3 -S-(CH 2 ) 2 CH 3 ), R 8 -NHC(O)-R 10 , -O-R 8 - R 10 , R 8 -(substituted or unsubstituted C 3 -C 8 cycloalkyl) (e.g., CH 2 -cyclopropyl, CH 2 -cyclobutanol, CH 2 - difluorocyclopropyl, CH 2 -methylcyclopropyl, CH 2 -dimethylamin
  • R is H, F, Cl, Br, I, OH, SH, alkoxy, NH(R 10 ), NH-CH 2 -cyclopropyl, N(R 10 )(R 11 ), CF 3 , CN, NO 2 , COOH, C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., methyl, ethyl, CH 2 -OH, CH 2 -CH 2 -OH, CH 2 -CH 2 -O-CH 2 -CH 2 ),
  • each R 8 is independently [CH 2 ] p wherein p is between 1 and 10;
  • R 9 is [CH] q , [C] q wherein q is between 2 and 10;
  • R 10 and R 11 are each independently H, C 1 -C 5 substituted or unsubstituted linear or branched alkyl (e.g., methyl, ethyl, CH 2 -cyclopropyl, CH 2 -CH 2 -O-CH 3 ), C 1 -C 5 substituted or unsubstituted linear or branched
  • X 2 of formula I, II and/or I(a)-I(o) is a nitrogen atom. In other embodiments, X 2 is a CH.
  • X 3 of formula I, II and/or I(a)-I(o) is a nitrogen atom. In other embodiments, X 3 is a CH.
  • X 4 of formula I, II and/or I(a)-I(o) is a nitrogen atom. In other embodiments, X 4 is a CH.
  • X 5 of formula I, II, I(a)-I(i), I(m) and/or I(o) is a nitrogen atom.
  • X 5 is a carbon atom.
  • X 6 of formula I, II, I(a)-I(i), I(m) and/or I(o) is a nitrogen atom. In other embodiments, X 6 is a carbon atom.
  • X 7 of formula I, II and/or I(a)-I(e) is a nitrogen atom. In other embodiments, X 7 is a carbon atom.
  • X 8 of formula I, II, I(a)-I(i), I(m) and/or I(o) is a nitrogen atom. In other embodiments, X 8 is a carbon atom.
  • X 9 of formula I, II, I(a)-I(i), I(m) and/or I(o) is a nitrogen atom. In other embodiments, X 9 is a carbon atom.
  • X 10 of formula I, II and/or I(a)-I(o) is a nitrogen atom. In other embodiments, X 10 is N. In other embodiments, X 10 is CH. In other embodiments, X 10 is C(R), wherein R is as defined below. In other embodiments, X 10 is C(R), wherein R is an alkyl. In other embodiments, X 10 is C(R), wherein R is a methyl.
  • X 10 is C(R), wherein R is a cycloalkyl. In other embodiments, X 10 is C(R), wherein R is a cyclopropyl. In other embodiments, X 10 is C(R), wherein R is a COOH. In other embodiments, X 10 is C(R), wherein R is N(H)R 10 ; and R 10 is a substituted alkyl. In other embodiments, X 10 is C(N(H)(CH 2 -cyclopropyl)). In other embodiments, X 10 is C(R), wherein R is a substituted alkyl. In other embodiments, X 10 is C(R), wherein R is CH 2 -OH.
  • X 10 is C(R), wherein R is CH 2 -CH 2 -OH. In other embodiments, X 10 is C(R), wherein R is an alkoxy. In other embodiments, X 10 is C(R), wherein R is a isopropoxy. [0052] In some embodiments, at least one of X 2 , X 3 , X 4 , X 5 , X 6 , X 7 , X 8 and X 9 of formula I, II, I(a)-I(e) is a nitrogen atom.
  • At least one of X 2 , X 3 , X 4 , X 5 , X 6 , X 8 and X 9 of formula I, II, I(a)-I(e), I(g)-I(i), I(m) and/or I(o) is a nitrogen atom.
  • at least one of X 2 , X 3 , X 4 , X 5 , X 6 , X 7 , X 8 and X 9 of formula I(d) is a nitrogen atom.
  • At least one of X 2 , X 3 , X 4 , X 5 , X 6 , X 7 , X 8 , X 9 and X 10 of formula I(d) is a nitrogen atom.
  • at least one of X 2 , X 3 , X 4 , and X 10 of formula I, II and/or I(a)-I(o) is a nitrogen atom.
  • at least one of X 2 , X 3 , X 4 and X 10 of formula I(d) is a nitrogen atom.
  • At least one of X 5 , X 6 , X 8 and X 9 of formula I, II and/or I(a)-I(o) is a nitrogen atom.
  • R 5 of formula I, II, I(a)-I(d), I(f)-I(i), I(l), I(n) and/or I(o) is H.
  • R 5 is C 1 -C 5 linear or branched alkyl. In other embodiments, R 5 is methyl.
  • R 5 is methyl, ethyl, propyl, isopropyl, butyl, t-butyl, iso-butyl, pentyl, neopentyl; each represents a separate embodiment according to this invention.
  • R 5 and R 6 of formula I, II, I(a)-I(i) and/or I(l) are joined to form a substituted or unsubstituted 5-8 membered heterocyclic ring.
  • R 5 and R 6 are joined to form a substituted 5-8 membered heterocyclic ring.
  • R 5 and R 6 are joined to form an unsubstituted 5-8 membered heterocyclic ring.
  • the heterocyclic ring is azepane, piperazine or 2-(piperazin-1-yl)acetamide; each represents a separate embodiment according to this invention.
  • the heterocyclic ring is substituted with at least one substitution selected from: F, Cl, Br, I, CF 3 , R 20 , C 1 -C 5 linear or branched alkyl, C 1 -C 5 linear or branched haloalkyl, OH, alkoxy , R 8 -OH (e.g., CH 2 -OH), OMe, amide , C(O)N(R) 2 , C(O)N(R 10 )(R 11 ), R 8 -C(O)N(R 10 )(R 11 ), C(O)-pyrrolidine, C(O)-piperidine, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), N(CH 3 ) 2 , NH 2 ,
  • the heterocyclic ring of formula I(e) is not substituted with CO 2 -R.
  • R 6 of formula I, II, I(a)-I(d), I(f)-I(i), I(l), I(n), and/or I(o) is H.
  • R 6 is H, F, Cl, Br, I, OH, SH, R 8 -OH, R 8 -SH, -R 8 -O-R 10 , CH 2 -O-CH 3 , (CH 2 ) 2 -O-CH 3 (CH 2 ) 3 -O-CH 3 , (CH 2 ) 2 -O-CH(CH 3 ) 2 , R 8 -S-R 10 , (CH 2 ) 3 -S-(CH 2 ) 2 CH 3 , R 8 -NHC(O)-R 10 , -O-R 8 -R 10 , R 8 - (substituted or unsubstituted C 3 -C 8 cycloalkyl), CH 2 -cyclopropyl, CH 2 -cyclobutanol, CH 2 - difluorocyclopropyl, CH 2 -methylcyclopropyl, CH 2 -dimethylamino-cyclohexyl, (CH 2 -cyclo
  • R 6 may be further substituted with at least one substitution selected from: F, Cl, Br, I, C 1 -C 5 linear or branched alkyl, OH, alkoxy , OMe, amide , C(O)N(R) 2 , C(O)-alkyl, C(O)-pyrrolidine, C(O)-piperidine, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), N(CH 3 ) 2 , NH 2 , CF 3 , aryl, phenyl, heteroaryl, substituted or unsubstituted C 3 -C 8 cycloalkyl , cyclobutanol, substituted or unsubstituted 3-8 membered heterocyclic ring pyran, oxetane, piperidine, pyrazole, methyl-pyrrazole, triazole, imidazole, C 1 -C 5 linear or branched hal
  • R 6 is H. In some embodiments, R 6 is -R 8 -O-R 10 . In some embodiments, R 6 is CH 2 -O-CH 3 . In some embodiments, R 6 is R 8 -S-R 10 . In some embodiments, R 6 is (CH 2 ) 3 -S-(CH 2 ) 2 CH 3 . In some embodiments, R 6 is R 8 -NHC(O)-R 10 . In some embodiments, R 6 is (CH 2 ) 3 - NHC(O)-R 10 . In some embodiments, R 6 is (CH 2 )-NHC(O)-R 10 .
  • R 6 is R 8 - (substituted or unsubstituted C 3 -C 8 cycloalkyl).
  • R 8 -(substituted or unsubstituted C 3 -C 8 cycloalkyl) include but not limited to: CH 2 -cyclobutanol, CH 2 -difluorocyclopropyl, CH 2 - methylcyclopropyl, CH 2 -dimethylamino-cyclohexyl, (CH 2 ) 2 -cyclopentanole, and CH 2 -cyclohexanol; each represents a separate embodiment according to this invention.
  • R 6 is R 8 - (substituted or unsubstituted saturated, unsaturated or aromatic, single, fused or spiro 3-8 membered heterocyclic ring). In some embodiments, R 6 is R 8 -(substituted or unsubstituted saturated, single 3-8 membered heterocyclic ring). In some embodiments, R 6 is R 8 -(substituted or unsubstituted unsaturated, single 3-8 membered heterocyclic ring). In some embodiments, R 6 is (CH 2 ) 3 -4-fluoro-piperidine.
  • R 6 is R 8 -(substituted or unsubstituted aromatic, single 3-8 membered heterocyclic ring). In some embodiments, R 6 is R 8 -(substituted or unsubstituted saturated, fused 3-8 membered heterocyclic ring). In some embodiments, R 6 is R 8 -(substituted or unsubstituted unsaturated, fused 3-8 membered heterocyclic ring). In some embodiments, R 6 is R 8 -(substituted or unsubstituted aromatic, fused 3-8 membered heterocyclic ring).
  • R 6 is R 8 -(substituted or unsubstituted spiro 3-8 membered heterocyclic ring).
  • R 8 -(substituted or unsubstituted saturated, unsaturated or aromatic, single, fused or spiro 3-8 membered heterocyclic ring) include but not limited to: (CH 2 ) 3 -4-fluoro-piperidine, (CH 2 ) 3 -pyran, (CH 2 ) 2 -pyrrazole, (CH 2 ) 2 -imidazole, CH 2 - tetrahydrofurane, CH 2 -dioxane, CH 2 -oxetane, CH 2 -piperidine, CH 2 -triazole, CH 2 -1-oxa-8- azaspiro[4.5]decane, (CH 2 ) 3 -diazabicyclo[2.2.1]heptane, CH 2 -methyl-THF, CH 2
  • R 6 is NH 2 . In some embodiments, R 6 is NHR. In some embodiments, R 6 is N(R) 2 . In some embodiments, R 6 is NH(R 10 ). In some embodiments, R 6 is N(R 10 )(R 11 ). In some embodiments, R 6 is R 8 -N(R 10 )(R 11 ).
  • R 8 -N(R 10 )(R 11 ) includes but not limited to: (CH 2 ) 3 -N(CH 2 CH 3 ) 2 , (CH 2 ) 3 -N(CH(CH 3 ) 2 ) 2 , (CH 2 ) 3 -piperidine, (CH 2 ) 4 - NH(CH 3 ), (CH 2 ) 3 -NH-CH 3 , (CH 2 ) 3 -NH-CH 2 CH 3 , (CH 2 ) 3 -N(CH 2 CH 3 ) 2 , (CH 2 ) 3 -NH 2 , and (CH 2 ) 3 - N(CH 2 CH 3 )(CH 2 CF 3 ).
  • R 6 is R 8 -C(O)N(R 10 )(R 11 ) such as (CH 2 ) 2 -C(O)- piperidine. In some embodiments, R 6 is C 1 -C 5 linear or branched, substituted or unsubstituted alkyl.
  • C 1 -C 5 linear or branched, substituted or unsubstituted alkyl examples include but not limited to: CH(CH 3 )CH 2 OCH 3 , CH(CH 3 )CH 2 NH 2 , CH(CH 3 )C(O)N(CH 3 ) 2 , CH 2 -CH(OH)Ph, (CH 2 ) 3 N(H)CH 2 CH 3 , CH(CH 3 )(CH 2 ) 2 OH, CH(CH 2 OH)(CH 2 CH 3 ), (CH 2 ) 3 -OCH 3 , (CH 2 ) 2 -OCH 3 , (CH 2 ) 2 -OCH 3 , (CH 2 ) 2 -OCH(CH 3 ) 2 , CH(CH 2 OH)(CH 2 CH(CH 3 ) 2 ), CH 2 CH(CH 3 )(OCH 3 ), CH 2 CH(N(CH 3 ) 2 )(CH 2 CH 3 ), CH(CH 3 )C(O)N(
  • R 6 is substituted or unsubstituted C 3 -C 8 cycloalkyl.
  • substituted or unsubstituted C3- C8 cycloalkyl include: cyclopropyl, cyclobutyl, cyclohexyl, methoxycyclopropyl, methylcyclobutyl, aminomethyl-cyclobutyl, methoxycyclobutyl and 2,3-dihydro-1H-indeno.
  • R 6 is R 8 -(substituted or unsubstituted C 3 -C 8 cycloalkyl).
  • R 6 is substituted or unsubstituted saturated or unsaturated, single fused, bridged or spiro 3-10 membered carbocyclic or heterocyclic ring.
  • the ring may be further substituted with at least one substitution selected from: F, Cl, Br, I, C 1 -C 5 linear or branched alkyl, OH, alkoxy , OMe, amide , C(O)N(R) 2 , C(O)- alkyl, C(O)-pyrrolidine, C(O)-piperidine, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), N(CH 3 ) 2 , NH 2 , CF 3 , aryl, phenyl, heteroaryl, substituted or unsubstituted C 3 -C 8 cycloalkyl , cyclobutanol, substituted or unsubstituted 3-8 membered heterocyclic ring
  • R 6 is substituted or unsubstituted saturated or unsaturated, single fused, bridged or spiro 3-10 membered heterocyclic ring. In some embodiments, R 6 is substituted or unsubstituted saturated, unsaturated or aromatic, single, fused or spiro 3-10 membered heterocyclic ring. In some embodiments, R 6 is substituted or unsubstituted saturated, unsaturated or aromatic, single 3-10 membered heterocyclic ring. In some embodiments, R 6 is substituted or unsubstituted saturated single 3-10 membered heterocyclic ring.
  • R 6 is substituted or unsubstituted saturated or unsaturated, single fused, bridged or spiro 3-10 membered carbocyclic ring. In some embodiments, R 6 is 4,4-difluorocyclohexane. In some embodiments, R 6 is substituted or unsubstituted R 8 -aryl, such as benzyl.
  • R 6 may be further substituted by at least one substitution selected from: F, Cl, Br, I, CF 3 , R 20 , C 1 -C 5 linear or branched alkyl, C 1 -C 5 linear or branched haloalkyl, OH, alkoxy , R 8 -OH (e.g., CH 2 -OH), OMe, amide , C(O)N(R) 2 , C(O)N(R 10 )(R 11 ), R 8 -C(O)N(R 10 )(R 11 ), C(O)-pyrrolidine, C(O)-piperidine, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), N(CH 3 ) 2 , NH 2 , CF 3 , aryl, phenyl, heteroaryl, substituted or unsubstituted C 3 -C 8 cycloalkyl , cyclobutanol, substitute
  • R 6 is 4-piperidine. In some embodiments, R 6 is azetidine. In some embodiments, R 6 is morpholine. In some embodiments, R 6 is tetrahydropyran. In some embodiments, R 6 is tetrahydrofurane. In some embodiments, R 6 is dioxane. In some embodiments, R 6 is 1,3-dioxane. In some embodiments, R 6 is pyrrolidine. In some embodiments, R 6 is substituted single 3-8 membered heterocyclic ring. In some embodiments, R 6 is 1-methylpiperidine. In some embodiments, R 6 is 3-fluoro-1-methylpiperidine. In some embodiments, R 6 is 1-methyl-azetidine.
  • R 6 is trifluoromethyl-oxetane. In some embodiments, R 6 is hydroxy- tetrahydrofurane. In some embodiments, R 6 is 1-(2,2,2-trifluoroethyl)piperidine. In some embodiments, R 6 is substituted or unsubstituted, unsaturated, single 3-8 membered heterocyclic ring. In some embodiments, R 6 is pyrrolidinone. In some embodiments, R 6 is imidazole. In some embodiments, R 6 is azepan-2-one. In some embodiments, R 6 is substituted or unsubstituted, saturated bridged 3-10 membered heterocyclic ring.
  • R 6 is quinuclidine. In some embodiments, R 6 is 8- methyl-8-azabicyclo[3.2.1]octane. In some embodiments, R 6 is azabicyclohexane. In some embodiments, R 6 is substituted or unsubstituted, saturated spiro 3-10 membered heterocyclic ring. In some embodiments, R 6 is azaspiro[3.3]heptane. In some embodiments, R 6 is substituted or unsubstituted C 3 -C 8 cycloalkyl. In some embodiments, R 6 is cyclopropyl In some embodiments, R 6 is 4,4- difluorocyclohexane.
  • R 6 and R 5 of formula I, II, I(a)-I(i), I(l), I(n) and/or I(o) are joined to form a substituted or unsubstituted saturated, unsaturated or aromatic, single, fused or spiro 5-8 membered heterocyclic ring.
  • the substituted or unsubstituted saturated, unsaturated or aromatic, single, fused or spiro 5-8 membered heterocyclic ring is azepane, piperazine, or 2-(piperazin-1-yl)acetamide; each represents a separate embodiment according to this invention.
  • the ring may be further substituted by at least one substitution selected from: F, Cl, Br, I, C 1 -C 5 linear or branched alkyl, OH, alkoxy (e.g., OMe), amide (e.g., C(O)N(R) 2 , C(O)-pyrrolidine, C(O)-piperidine, N(R) 2 NH(R 10 ), N(R 10 )(R 11 ), (e.g., N(CH 3 ) 2 , NH 2 ), CF 3 , aryl, phenyl, heteroaryl, substituted or unsubstituted C 3 -C 8 cycloalkyl (e.g., cyclobutanol), substituted or unsubstituted 3-8 membered heterocyclic ring (e.g.
  • pyran oxetane, piperidine, pyrazole, methyl-pyrrazole, triazole, imidazole), C 1 -C 5 linear or branched haloalkyl (e.g., CH 2 CF 3 , CHF 2 ), halophenyl, (benzyloxy)phenyl, CN and NO 2 ; each represents a separate embodiment according to this invention.
  • C 1 -C 5 linear or branched haloalkyl e.g., CH 2 CF 3 , CHF 2
  • halophenyl e.g., (benzyloxy)phenyl
  • CN and NO 2 each represents a separate embodiment according to this invention.
  • R 6 of formula I, II and/or I(a)-I(i) is represented by the structure of formula B: wherein m is 0 or 1; and R 12 is R 20 or C 1 -C 5 C(O)-alkyl, and R 13 is R 30 ; or R 12 and R 13 are both H; or R 12 and R 13 are each independently H or substituted or unsubstituted C 1 -C 5 alkyl (e.g., ethyl, trifluoroethyl); or R 12 and C3 are joined to form ring A and R 13 is R 30 ; or R 12 and R 13 are joined to form ring B; or R 12 and C1 are joined to form ring C and R 13 is R 30 ; or C1 and C3 are joined to form ring D and R 12 and R 13 are each independently R 30 ; or R 13 and C2 are joined to form ring E, m is 1, and R 12 is R 30 ; or R 12 and R 13 are joined to form ring
  • R 6 of formula I, II and/or I(a)-I(i) is represented by the structure of formula Bi: wherein m is 0 or 1; and R 12 is R 20 or C 1 -C 5 C(O)-alkyl, and R 13 is R 30 ; or R 12 and R 13 are both H; or R 12 and R 13 are each independently H or substituted or unsubstituted C 1 -C 5 alkyl (e.g., ethyl, trifluoroethyl); or R 12 and C3 are joined to form ring A and R 13 is R 30 ; or R 12 and R 13 are joined to form ring B; or R 12 and C1 are joined to form ring C and R 13 is R 30 ; or C1 and C3 are joined to form ring D and R 12 and R 13 are each independently R 30 ; or R 13 and C2 are joined to form ring E, m is 1, and R 12 is R 30 ; or R 12 and R 13 are joined to form ring E, m is 1,
  • R 12 is R 20 . In other embodiments, R 12 is R 30 . In some embodiments, R 12 is C 1 -C 5 C(O)-alkyl. In some embodiments, R 12 is substituted or unsubstituted C 1 -C 5 alkyl. In some embodiments, R 12 is unsubstituted C 1 -C 5 alkyl. In some embodiments, the alkyl is ethyl. In some embodiments, R 12 is substituted C 1 -C 5 alkyl. In some embodiments,the alkyl is trifluoroethyl. [0063] In some embodiments, R 13 of formula B and/or Bi is H. In other embodiments, R 13 is R 30 .
  • R 13 is substituted or unsubstituted C 1 -C 5 alkyl. In some embodiments, R 13 is unsubstituted C 1 -C 5 alkyl. In some embodiments, the alkyl is ethyl. In some embodiments, R 13 is substituted C 1 -C 5 alkyl. In some embodiments,the alkyl is trifluoroethyl. [0064] In some embodiments, R 6 of formula I, II and/or I(a)-I(i) is represented by formula B. In some embodiments, R 12 of formula B is R 20 or C 1 -C 5 C(O)-alkyl, and R 13 is R 30 .
  • R 12 and R 13 of formula B are both H.
  • R and R of formula B are each independently H or substituted or unsubstituted C 1 -C 5 alkyl (e.g., ethyl, trifluoroethyl).
  • R 12 and R 13 of formula B are each independently H or trifluoroethyl.
  • R 12 and C3 of formula B are joined to form ring A and R 13 is R 30 .
  • R 12 and R 13 of formula B are joined to form ring B.
  • R 12 and C1 of formula B are joined to form ring C and R 13 is R 30 .
  • R 12 and R 13 of formula Bi are both H.
  • R 12 and R 13 of formula Bi are each independently H or substituted or unsubstituted C 1 -C 5 alkyl (e.g., ethyl, trifluoroethyl).
  • R 12 and R 13 of formula Bi are each independently H or trifluoroethyl.
  • R 12 and C3 of formula Bi are joined to form ring A and R 13 is R 30 .
  • R 12 and R 13 of formula Bi are joined to form ring B.
  • R 12 and C1 of formula Bi are joined to form ring C and R 13 is R 30 .
  • C1 and C3 of formula Bi are joined to form ring D and R 12 and R 13 of formula Bi are each independently R 30 .
  • R 13 and C2 of formula Bi are joined to form ring E, m is 1, and R 12 of formula Bi is R 30 .
  • R 12 and R 13 of formula Bi are joined to form ring B and C1 and C3 of formula Bi are joined to form ring D.
  • R 6 of formula I(g) is represented by the structure of formula C: wherein k is an integer number between 1 and 4; R 12 and R 13 are each independedntly H, C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., ethyl, isopropyl), R 20 , or R 12 and R 13 are joined to form a substituted or unsubstituted 4-7 membered heterocyclic ring (e.g., piperidine, piperazine, pyrrolidine, oxa-6-azaspiro[3.3]heptane).
  • k of formula C is 1.
  • R 12 and R 13 of formula C are each independently H, C 1 -C 5 linear or branched, substituted or unsubstituted alkyl (e.g., ethyl, isopropyl) or R 20 ; each represents a separate embodiment according to this invention.
  • R 12 and R 13 of formula C are both ethyls.
  • R 12 and R 13 of formula C are both isopropyls.
  • R 12 and R 13 of formula C are both alkyls.
  • R 12 and R 13 of formula C are joined to form a substituted or unsubstituted 4-7 membered heterocyclic ring.
  • R 12 and R 13 of formula C are joined to form a piperidine, piperazine, pyrrolidine, oxa-6-azaspiro[3.3]heptane; each represents a separate embodiment according to this invention.
  • the heterocyclic ring maybe further substituted with at least one substitution as defined herein for heterocyclic rings.
  • R 6 of formula I(b) is represented by formula Bi and/or B and R 12 of formula Bi and/or B is R 20 or C 1 -C 5 C(O)-alkyl
  • R 13 of formula Bi and/or B is R 30 ; or R 12 and R 13 are both H, or R 12 and R 13 are each independently H or trifluoroethyl; or R 12 and C3 are joined to form ring A and R 13 is R 30 ; or R 12 and R 13 are joined to form a substituted or unsubstituted pyrrolidine ring, piperazine, thiomorpholine 1,1-dioxide 2-oxa-6-azaspiro[3.3]heptane, pyrazole, imidazole, 2,5- diazabicyclo[2.2.1]heptane or a diazabicyclo[2.2.1]heptane; or R 12 and C1 are joined to form ring C and R 13 is R 30 ; or C1 and C3 are
  • R 6 of formula I(b) is represented by formula Bi and/or B and R 12 of formula Bi and/or B is R 20 or C 1 -C 5 C(O)-alkyl
  • R 13 of formula Bi and/or B is R 30 ; or R 12 and C3 are joined to form ring A and R 13 is R 30 ; or R 12 and R 13 are joined to form a substituted or unsubstituted pyrrolidine ring, piperazine, thiomorpholine 1,1-dioxide 2-oxa-6-azaspiro[3.3]heptane, pyrazole, imidazole, 2,5- diazabicyclo[2.2.1]heptane or a diazabicyclo[2.2.1]heptane; or R 12 and C1 are joined to form ring C and R 13 is R 30 ; or C1 and C3 are joined to form ring D and R 12 and R 13 are each independently R 30 ; or R 13 and C2 are joined to form
  • ring A of formula Bi is a substituted or unsubstituted single spiro or fused 3-8 membered heterocyclic ring. In some embodiments, ring A, is an unsubstituted single 3-8 membered heterocyclic ring. In some embodiments, ring A, is an unsubstituted spiro 3-8 membered heterocyclic ring. In some embodiments, ring A, is an unsubstituted fused 3-8 membered heterocyclic ring. In some embodiments, ring A, is a substituted single 3-8 membered heterocyclic ring.
  • ring A is a substituted spiro 3-8 membered heterocyclic ring. In some embodiments, ring A, is a substituted fused 3-8 membered heterocyclic ring. In some embodiments, ring A is: pyrrolidine, methylpyrrolidine, ethylpyrrolidine, 2-oxopyrrolidine, piperidine, methylpiperidine, methyl-2- oxopyrrolidine, pyran- azetidine, methyl-azetidine, azabicyclooctane, 2-azabicyclo[2.1.1]hexane, or 2- azaspiro[3.3]heptane; each represents a separate embodiment according to this invention.
  • ring B is a substituted single 3-8 membered heterocyclic ring. In some embodiments, ring B, is a substituted spiro 3-8 membered heterocyclic ring. In some embodiments, ring B, is a substituted fused 3-8 membered heterocyclic ring.
  • ring B is: pyrrolidine, methylpyrrolidine, ethylpyrrolidine, 2-oxopyrrolidine, hydroxymethyl-pyrrolidine, piperidine, piperidin-2-one, 4-fluoropiperidin-2-one, piperidine-4-carbonitrile, methylpiperidine, fluoropiperidine, 4-fluoropiperidine, 4-fluoro-2-methylpiperidine, difluoropiperidine, piperazine, methyl-piperazine, dimethyl-pyrazole, methyl-2-oxopyrrolidine, pyran-, azetidine, methyl-azetidine, imidazole, azabicyclooctane, 2-azabicyclo[2.1.1]hexane, or 2-azaspiro[3.3]heptane, diazabicyclo[2.2.1]heptane, 2- methyl-2,5-diazabicyclo[2.2.1]heptane, thiomorpholine, or 1,1-dioxid
  • ring B is: piperidine, methyl-piperidin, fluoropiperidine, difluoropiperidine, pyrrolidine, piperazine, methylpyrrolidine, thiomorpholine, methyl-piperazine, dimethyl-pyrazole, imidazole, 2-methyl-2,5- diazabicyclo[2.2.1]heptane, 1,1-dioxide-2-oxa-6-azaspiro[3.3]heptane, hydroxymethyl-pyrrolidine or diazabicyclo[2.2.1]heptane, 6-fluoro-3-azabicyclo[3.1.1]heptane; each represents a separate embodiment according to this invention.
  • ring C of formula Bi is a substituted or unsubstituted single spiro or fused 3-8 membered heterocyclic ring. In some embodiments, ring C, is an unsubstituted single 3-8 membered heterocyclic ring. In some embodiments, ring C, is an unsubstituted spiro 3-8 membered heterocyclic ring. In some embodiments, ring C, is an unsubstituted fused 3-8 membered heterocyclic ring. In some embodiments, ring C, is a substituted single 3-8 membered heterocyclic ring.
  • ring C is a substituted spiro 3-8 membered heterocyclic ring. In some embodiments, ring C, is a substituted fused 3-8 membered heterocyclic ring. In some embodiments, ring C is: pyrrolidine, methylpyrrolidine, ethylpyrrolidine, 2-oxopyrrolidine, piperidine, methylpiperidine, methyl-2- oxopyrrolidine, pyran- azetidine, methyl-azetidine, azabicyclooctane, 2-azabicyclo[2.1.1]hexane, or 2- azaspiro[3.3]heptane; each represents a separate embodiment according to this invention.
  • ring C is: piperidine, pyrrolidine, methyl-2-oxopyrrolidine, pyran-pyrrolidine, methyl- azetidine, azabicyclooctane, 2-azabicyclo[2.1.1]hexane, or 2-azaspiro[3.3]heptane; each represents a separate embodiment according to this invention.
  • ring D of formula Bi is a substituted or unsubstituted C 3 -C 8 cycloalkyl. In some embodiments, ring D, is a substituted C 3 -C 8 cycloalkyl.
  • ring D is an unsubstituted C 3 -C 8 cycloalkyl.
  • ring D is cyclopropane, cyclobutane, cyclopentane, cyclohexane or cycloheptane; each represents a separate embodiment according to this invention.
  • ring E of formula Bi is a substituted or unsubstituted single spiro or fused 3-8 membered heterocyclic ring.
  • ring E is an unsubstituted single 3-8 membered heterocyclic ring.
  • ring E is an unsubstituted spiro 3-8 membered heterocyclic ring. In some embodiments, ring E, is an unsubstituted fused 3-8 membered heterocyclic ring. In some embodiments, ring E, is a substituted single 3-8 membered heterocyclic ring. In some embodiments, ring E, is a substituted spiro 3-8 membered heterocyclic ring. In some embodiments, ring E, is a substituted fused 3-8 membered heterocyclic ring.
  • R 6 of formula I(b) is F, Cl, Br, I, OH, SH, R 8 -OH, R 8 -SH, -R 8 -O-R 10 , CH 2 -O-CH 3 , R 8 -S-R 10 , (CH 2 ) 3 -S-(CH 2 ) 2 CH 3 , R 8 -NHC(O)-R 10 , -O-R 8 -R 10 , R 8 -(substituted or unsubstituted C 3 -C 8 cycloalkyl), CH 2 -cyclobutanol, CH 2 -difluorocyclopropyl, CH 2 -methylcyclopropyl, CH 2 -dimethylamino-cyclohexyl, (CH 2 ) 2 -cyclopentanole, CH 2 -cyclohexanol, (CH 2 ) 3 -pyran, CH 2 - tetrahydrofur
  • R 6 may be further substituted with at least one substitution selected from: F, Cl, Br, I, C 1 -C 5 linear or branched alkyl, OH, alkoxy (e.g., OMe), amide (e.g., C(O)N(R) 2 ), C(O)-alkyl, C(O)-pyrrolidine, C(O)-piperidine, N(R) 2 (e.g., N(CH 3 ) 2 , NH 2 ), NH(R 10 ), N(R 10 )(R 11 ), CF 3 , aryl, phenyl, heteroaryl, substituted or unsubstituted C 3 -C 8 cycloalkyl (e.g., cyclobutanol), substituted or unsubstituted 3-8 membered heterocyclic ring (e.g.
  • R 6 of formula I(b) and/or I(l) is -R 8 -O-R 10 .
  • -R 8 - O-R 10 is CH 2 -O-CH 3 .
  • R 6 is R 8 -S-R 10 .
  • R 6 is C 1 -C 5 linear or branched, substituted or unsubstituted alkyl. In some embodiments, R 6 is C 1 -C 5 linear or branched, substituted alkyl. In some embodiments, the substituted alkyl is CH(CH 3 )CH 2 OCH 3 , CH(CH 3 )CH 2 NH 2 , CH(CH 3 )C(O)N(CH 3 ) 2 , CH 2 -CH(OH)Ph, (CH 2 ) 3 N(H)CH 2 CH 3 , CH(CH 3 )(CH 2 ) 2 OH, CH(CH 2 OH)(CH 2 CH 3 ), (CH 2 ) 3 -OCH 3 , (CH 2 ) 2 -OCH 3 , (CH 2 ) 2 -OCH 3 , (CH 2 ) 2 -OCH(CH 3 ) 2 , CH(CH 2 OH)(CH 2 CH(CH 3 ) 2 ), CH 2 CH(CH 3 )(OCH
  • R 6 is C 1 -C 5 linear or branched, unsubstituted alkyl.
  • the unsubstituted alkyl is methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, pentyl, or neopentyl; each represents a separate embodiment according to this invention.
  • R 6 is substituted or unsubstituted C 3 -C 8 cycloalkyl. In some embodiments, R 6 is substituted C 3 -C 8 cycloalkyl.
  • the substituted cycloalkyl is methoxycyclopropyl, methylcyclobutyl, aminomethyl-cyclobutyl, or methoxycyclobutyl, 2,3-dihydro-1H-indenol; each represents a separate embodiment according to this invention.
  • R 6 is unsubstituted C 3 -C 8 cycloalkyl.
  • the unsubstituted cycloalkyl is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl or cyclooctyl; each represents a separate embodiment according to this invention.
  • R 6 is substituted or unsubstituted saturated or unsaturated, single fused, bridged or spiro 3-10 membered carbocyclic or heterocyclic ring.
  • R 6 the carbocyclic or heterocyclic ring as defined in R 6 is further substituted with at least one substitution selected from: F, Cl, Br, I, C 1 -C 5 linear or branched alkyl, OH, alkoxy (e.g., OMe), amide , C(O)N(R) 2 , C(O)-alkyl, C(O)- pyrrolidine, C(O)-piperidine, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), N(CH 3 ) 2 , NH 2 , CF 3 , aryl, phenyl, heteroaryl, substituted or unsubstituted C 3 -C 8 cycloalkyl (e.g., cyclobut
  • R 6 is piperidine. In some embodiments, R 6 is 1-methylpiperidine. In some embodiments, R 6 is 3-fluoro-1-methylpiperidine. In some embodiments, R 6 is 1-(2,2,2- trifluoroethyl)piperidine, In some embodiments, R 6 is azetidine. In some embodiments, R 6 is 1-methyl- azetidine. In some embodiments, R 6 is morpholine. In some embodiments, R 6 is pyrrolidine. In some embodiments, R 6 is pyrrolidinone. In some embodiments, R 6 is tetrahydropyran. In some embodiments, R 6 is tetrahydrofurane.
  • R 6 is 8-methyl-8-azabicyclo[3.2.1]octane. In some embodiments, R 6 is dioxane. In some embodiments, R 6 is 1,3-dioxane. In some embodiments, R 6 is substituted or unsubstituted saturated or unsaturated, single fused, bridged or spiro 3-10 membered carbocyclic ring. In some embodiments, R 6 is 4,4-difluorocyclohexane.
  • R 7 of formula I, II, I(a)-I(f) and/or I(i) is H, F, Cl, Br, I, OH, O-R 20 , SH, R 8 -OH, R 8 -SH, SR 10 , -R 8 -O-R 10 , -R 8 -S-R 10 , R 8 -(C 3 -C 8 cycloalkyl), R 8 -(3-8 membered heterocyclic ring), CF 3 , CD 3 , OCD 3 , CN, NO 2 , -CH 2 CN, -R 8 CN, NH 2 , NHR, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), R 8 -N(R 10 )(R 11 ), R 9 -R 8 -N(R 10 )(R 11 ), B(OH) 2 , -OC(O)CF 3 , -OCH 2 Ph
  • R 7 is further substituted with at least one substitution selected from: F, Cl, Br, I, C 1 -C 5 linear or branched alkyl, OH, alkoxy (e.g., OMe), amide (e.g., C(O)N(R) 2 ), C(O)- alkyl, C(O)-pyrrolidine, C(O)-piperidine, N(R) 2 NH(R 10 ), N(R 10 )(R 11 ), (e.g., N(CH 3 ) 2 , NH 2 ), CF 3 , aryl, phenyl, heteroaryl, substituted or unsubstituted C 3 -C 8 cycloalkyl (e.g., cyclobutanol), substituted or unsubstituted 3-8 membered heterocyclic ring (e.g.
  • R 7 of formula I, II, I(b), I(d)-I(f) and/or I(i) is H.
  • R 7 is F.
  • R 7 is Cl.
  • R 7 is Br.
  • R 7 is I.
  • R 7 is OH.
  • R 7 is O-R 20 .
  • R 7 is CF 3 .
  • R 7 is CN. In some embodiments, R 7 is NH 2 . In some embodiments, R 7 is NHR. In some embodiments, R 7 is N(R) 2 . In some embodiments, R 7 is NH(R 10 ). In some embodiments, R 7 is N(R 10 )(R 11 ). In some embodiments, R 7 is NHC(O)-R 10 . In some embodiments, R 7 is COOH. In some embodiments, R 7 is -C(O)Ph. In some embodiments, R 7 is C(O)O-R 10 . In some embodiments, R 7 is COO-CH 3. In some embodiments, R 7 is C(O)H. In some embodiments, R 7 is C(O)-R 10 .
  • R 7 is C 1 -C 5 linear or branched C(O)-haloalkyl. In some embodiments, R 7 is -C(O)NH 2 . In some embodiments, R 7 is C(O)NHR. In some embodiments, C(O)NHR is C(O)NH(CH 3 ). In some embodiments, R 7 is C(O)N(R 10 )(R 11 ). In some embodiments, C(O)N(R 10 )(R 11 ) is C(O)NH(CH 3 ), C(O)NH(CH 2 CH 2 OCH 3 ), or C(O)NH(CH 2 CH 2 OH); each represents a separate embodiment according to this invention. In some embodiments, R 7 is SO 2 R.
  • R 7 is C 1 -C 5 linear or branched, substituted or unsubstituted alkyl.
  • the alkyl is methylimidazole, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, pentyl, neopentyl or hexyl; each represents a separate embodiment according to this invention.
  • R 7 is C 1 -C 5 linear or branched, or C 3 -C 8 cyclic haloalkyl. In some embodiments, R 7 is C 1 -C 5 linear haloalkyl.
  • the haloalkyl is CHF 2 .
  • R 7 is C 1 -C 5 branched haloalkyl.
  • R 7 is C 3 -C 8 cyclic haloalkyl.
  • R 7 is C 1 -C 5 linear or branched, or C3- C8 cyclic alkoxy optionally wherein at least one methylene group (CH 2 ) in the alkoxy is replaced with an oxygen atom.
  • R 7 is C 1 -C 5 linear alkoxy.
  • the alkoxy is methoxy. In some embodiments, the alkoxy is ethoxy.
  • R 7 is C 1 -C 5 branched alkoxy. In some embodiments, R 7 is C 3 -C 8 cyclic alkoxy. In some embodiments, R 7 is C 1 -C 5 linear or branched thioalkyl. In some embodiments, R 7 is C 1 -C 5 linear or branched haloalkoxy. In some embodiments, R 7 is C 1 -C 5 linear haloalkoxy. In some embodiments, R 7 is C 1 -C 5 branched haloalkoxy. In some embodiments, R 7 is C 1 -C 5 linear or branched alkoxyalkyl.
  • R 7 is substituted or unsubstituted C 3 -C 8 cycloalkyl.
  • the cycloalkyl is cyclopropyl, cyclopropanol, cyclobutyl, cyclopentyl, bicyclo[1.1.1]pentane, cyclohexyl, cycloheptyl or cyclooctyl; each represents a separate embodiment according to this invention.
  • R 7 is substituted or unsubstituted 3-10 membered single, fused, bridged or spiro, saturated, unsaturated or aromatic, carbocyclic or heterocyclic ring.
  • R 7 is substituted or unsubstituted 3- 10 membered single, fused, bridged or spiro, saturated, unsaturated or aromatic heterocyclic ring. In some embodiments, R 7 is substituted or unsubstituted 4-7 membered heterocyclic ring. In some embodiments, R 7 is unsubstituted 4-7 membered heterocyclic ring.
  • R 7 is a substituted or unsubstituted 3-10 membered bridged, fused or spiro heterocyclic ring.
  • the ring is 4-azaspiro[2.4]heptane, 2-oxa-5-azaspiro[3.4]octane, 1,4-dioxa-6-azaspiro[4.4]nonane, 4,7- diazaspiro[2.5]octane, 2,5-diazabicyclo[2.2.1]heptane; each represents a separate embodiment according to this invention.
  • R 7 is R 8 -(substituted or unsubstituted single, fused or spiro 3-8 membered heterocyclic ring). In some embodiments, R 7 is R 8 -(unsubstituted single 3-8 membered heterocyclic ring). In some embodiments, R 7 is R 8 -(unsubstituted fused 3-8 membered heterocyclic ring). In some embodiments, R 7 is R 8 -(unsubstituted spiro 3-8 membered heterocyclic ring). In some embodiments, R 7 is R 8 -(substituted single 3-8 membered heterocyclic ring).
  • R 7 is R 8 -(substituted fused 3-8 membered heterocyclic ring). In some embodiments, R 7 is R 8 -(substituted spiro 3-8 membered heterocyclic ring). In some embodiments, the heterocyclic ring may be saturated. In some embodiments, the heterocyclic ring may be unsaturated. In some embodiments, the hetrocyclic ring may be aromatic. In some embodiments, R 7 is substituted or unsubstituted aryl. In some embodiments, R 7 is phenyl.
  • R 7 may be further substituted with at least one substitution selected from: F, Cl, Br, I, C 1 -C 5 linear or branched alkyl, OH, alkoxy (e.g., OMe), amide (e.g., C(O)N(R) 2 , C(O)-pyrrolidine, C(O)-piperidine, N(R) 2 NH(R 10 ), N(R 10 )(R 11 ), (e.g., N(CH 3 ) 2 , NH 2 ), CF 3 , aryl, phenyl, heteroaryl, substituted or unsubstituted C 3 -C 8 cycloalkyl (e.g., cyclobutanol), C 1 -C 5 linear or branched haloalkyl (e.g., CH 2 CF 3 , CHF 2 ), substituted or unsubstituted 3-8 membered heterocyclic ring (e.g.
  • R 7 of formula I(a) is O-R 20 .
  • R 7 is substituted or unsubstituted 4-7 membered heterocyclic ring.
  • R 7 is substituted or unsubstituted 3-10 membered single, fused, bridged or spiro, saturated, unsaturated or aromatic, carbocyclic or heterocyclic ring.
  • R 7 is substituted or unsubstituted 3-10 membered single, fused, bridged or spiro, saturated, unsaturated or aromatic heterocyclic ring. In some embodiments, R 7 is substituted or unsubstituted 4-7 membered heterocyclic ring. In some embodiments, R 7 is unsubstituted 4-7 membered heterocyclic ring.
  • the heterocyclic ring is morpholine, tetrahydrofuran, tetrahydropyran, oxetane, pyrrolidine, pyrrolidin-3-one, pyrrolidin-2-one, pyrrolidinone, imidazole, pyrazole, isoxazolidine, piperazine, piperidine, piperidine-2-one, oxadiazole, triazole, isoxazolidine, or 2-oxopyrrolidine; each represents a separate embodiment according to this invention.
  • R 7 is substituted 4-7 membered heterocyclic ring.
  • the heterocyclic ring is 3,3-dimethylmorpholine, oxetan-3-ol, pyrrolidin-2-ol, pyrrolidin- 3-ol, 3-methoxypyrrolidine, pyrrolidine-3-carbonitrile, 3-cyanopyrrolidine, 1-methylpyrrolidine, 2,2- dimethylpyrrolidine, 3,3-difluoropyrrolidine, difluoromethylpyrrolidine, pyrrolidin-3-one-O- methyloxime, pyrrolidin-3-one O-methyl oxime, 1-methylpiperazine, 1-methylpiperazine, piperidin-3- ol, piperidin-4-ol, piperidine-4-carbonitrile, 4-fluoropiperidine; each represents a separate embodiment according to this invention.
  • R 7 is a substituted or unsubstituted 3-10 membered bridged, fused or spiro heterocyclic ring.
  • the ring is 4-azaspiro[2.4]heptane, 2- oxa-5-azaspiro[3.4]octane, 1,4-dioxa-6-azaspiro[4.4]nonane; each represents a separate embodiment according to this invention.
  • R 7 is morpholine.
  • R 7 is tetrahydrofuran.
  • R 7 is tetrahydropyran.
  • R 7 is oxetane.
  • R 7 is oxetan-3-ol. In some embodiments, R 7 is pyrrolidine. In some embodiments, R 7 is pyrrolidin-2-ol. In some embodiments, R 7 is pyrrolidin-3-ol. In some embodiments, R 7 is 3- methoxypyrrolidine. In some embodiments, R 7 is pyrrolidine-3-carbonitrile. In some embodiments, R 7 is 1-methylpyrrolidine. In some embodiments, R 7 is pyrrolidin-2-one. In some embodiments, R 7 is pyrrolidin-3-one. In some embodiments, R 7 is pyrrolidinone. In some embodiments, R 7 is imidazole. In some embodiments, R 7 is pyrazole.
  • R 7 is isoxazolidine. In some embodiments, R 7 is piperazine. In some embodiments, R 7 is piperidine. In some embodiments, R 7 is piperidin-3-ol. In some embodiments, R 7 is piperidin-4-ol. In some embodiments, R 7 is piperidine-2-one. In some embodiments, R 7 is piperazine-2-one. In some embodiments, R 7 is piperidine-4-carbonitrile. In some embodiments, R 7 is 4-fluoropiperidine. In some embodiments, R 7 is 2,2-dimethylpyrrolidine. In some embodiments, R 7 is pyrrolidin-3-one O-methyl oxime.
  • R 7 is a substituted or unsubstituted 3-10 membered bridged, fused or spiro heterocyclic ring.
  • R 7 is 4- azaspiro[2.4]heptane.
  • R 7 is 2-oxa-5-azaspiro[3.4]octane.
  • R 7 is 1,4-dioxa-6-azaspiro[4.4]nonane.
  • R 7 is 4,7-diazaspiro[2.5]octane.
  • R 7 is 2,5-diazabicyclo[2.2.1]heptane.
  • R 7 is 3,3- dimethylmorpholine.
  • R 7 is 1-methylpiperazine. In some embodiments, R 7 is oxadiazole. In some embodiments, R 7 is triazole. In some embodiments, R 7 is substituted or unsubstituted aryl. In some embodiments, R 7 is phenyl.
  • R 7 may be further substituted with at least one substitution selected from F, Cl, Br, I, C 1 -C 5 linear or branched alkyl, OH, alkoxy (e.g., OMe), amide (e.g., C(O)N(R) 2 , C(O)-pyrrolidine, C(O)-piperidine, N(R) 2 NH(R 10 ), N(R 10 )(R 11 ), (e.g., N(CH 3 ) 2 , NH 2 ), CF 3 , aryl, phenyl, heteroaryl, substituted or unsubstituted C 3 -C 8 cycloalkyl (e.g., cyclobutanol), substituted or unsubstituted 3-8 membered heterocyclic ring (e.g.
  • pyran oxetane, piperidine, pyrazole, methyl-pyrrazole, triazole, imidazole), C 1 -C 5 linear or branched haloalkyl (e.g., CH 2 CF 3 , CHF 2 ), halophenyl, (benzyloxy)phenyl, CN and NO 2 ; each represents a separate embodiment according to this invention.
  • C 1 -C 5 linear or branched haloalkyl e.g., CH 2 CF 3 , CHF 2
  • halophenyl e.g., (benzyloxy)phenyl
  • CN and NO 2 each represents a separate embodiment according to this invention.
  • R 7 of formula I(c) is not H, F, Cl, C 1 -C 5 linear or branched, or C 3 -C 8 cyclic alkoxy, C 1 -C 5 linear or branched haloalkoxy or C 1 -C 5 linear or branched, substituted or unsubstituted alkyl.
  • R 7 of formula I, II, I(a)-I(f) and/or I(i) is represented by the structure of formula A: wherein X 1 is N or O; R 1 and R 2 are each independently H, F, Cl, Br, I, OH, SH, or CF 3 , substituted or unsubstituted C 1 -C 5 alkyl (e.g., CH 2 OH, CH 2 OCH 3 ), C 1 -C 5 linear or branched, or C 3 -C 8 cyclic haloalkyl, substituted or unsubstituted C 1 -C 5 linear or branched, or C 3 -C 8 cyclic alkoxy, 3-8 membered carbocyclic or heterocyclic ring (e.g., oxetane); or R 1 and R 2 are joined to form a C 3 -C 8 carbocyclic or heterocyclic ring (e.g., cyclopropyl); R 3 and R 3 and R
  • X 1 is O.
  • R 1 of formula A, I(h), I(m), and/or I(o) is H.
  • R 1 is F.
  • R 1 is CF 3 .
  • R 1 is Cl.
  • R 1 is Br.
  • R 1 is I.
  • R 1 is OH.
  • R 1 is SH.
  • R 1 is substituted or unsubstituted C 1 -C 5 alkyl.
  • R 1 is CH 2 OH.
  • R 1 is CH 2 OCH 3 .
  • R 1 is C 1 -C 5 linear or branched, or C 3 -C 8 cyclic haloalkyl. In other embodiments, R 1 is substituted or unsubstituted C 1 -C 5 linear or branched, or C 3 -C 8 cyclic alkoxy. In other embodiments, R 1 is 3-8 membered carbocyclic or heterocyclic ring. In other embodiments, R 1 is 3-8 membered heterocyclic ring. In other embodiments, R 1 is oxetane. In other embodiments, R 1 is 3-8 membered carbocyclic ring. [0086] In some embodiments, R 2 of formula A, I(h), I(m), and/or I(o) is H.
  • R 2 is F. In other embodiments R 2 is CF 3 . In other embodiments, R 2 is Cl. In other embodiments, R 2 is Br. In other embodiments, R 2 is I. In other embodiments, R 2 is OH. In other embodiments, R 2 is SH. In other embodiments, R 2 is substituted or unsubstituted C 1 -C 5 alkyl. In other embodiments, R 2 is CH 2 OH. In other embodiments, R 2 is CH 2 OCH 3 . In other embodiments, R 2 is C 1 -C 5 linear or branched, or C 3 -C 8 cyclic haloalkyl.
  • R 3 is substituted or unsubstituted C 1 -C 5 alkyl.
  • the alkyl is methoxyethylene, methylaminoethylene, aminoethylene; each represents a separate embodiment according to this invention.
  • R 3 is -R 8 -O-R 10 .
  • R 3 is (CH 2 ) 2 -O-CH 3 ).
  • R 3 is R 8 -N(R 10 )(R 11 ).
  • R 3 is (CH 2 ) 2 - NH(CH 3 ).
  • R 3 is substituted or unsubstituted C 3 -C 8 cycloalkyl.
  • the cycloalkyl is cyclopropyl.
  • R 3 is substituted or unsubstituted 5- 7 membered heterocyclic ring.
  • the heterocyclic ring is pyrrolidine, methylpyrrolidine, or piperidine; each represents a separate embodiment according to this invention.
  • R 3 is pyrrolidine.
  • R 3 is methylpyrrolidine.
  • R 3 is piperidine.
  • R 3 is R 20 as defined hereinbelow.
  • R 4 of formula A, I(h), I(m), and/or I(o) is H.
  • R 4 is methyl.
  • R 4 is substituted or unsubstituted C 1 -C 5 alkyl.
  • the alkyl is methoxyethylene, methylaminoethylene, aminoethylene; each represents a separate embodiment according to this invention.
  • R 4 is -R 8 -O-R 10 .
  • R 4 is (CH 2 ) 2 -O-CH 3 ).
  • R 4 is R 8 -N(R 10 )(R 11 ).
  • R 4 is (CH 2 ) 2 - NH(CH 3 ).
  • R 4 is substituted or unsubstituted C 3 -C 8 cycloalkyl.
  • the cycloalkyl is cyclopropyl.
  • R 4 is substituted or unsubstituted 5- 7 membered heterocyclic ring.
  • the heterocyclic ring is pyrrolidine, methylpyrrolidine, or piperidine; each represents a separate embodiment according to this invention.
  • R 4 is pyrrolidine.
  • R 4 is methylpyrrolidine.
  • R 4 is piperidine.
  • R 4 is R 20 as defined hereinbelow.
  • R 3 and R 4 of formula A, I(h), I(m), and/or I(o) are joined to form a 3-8 membered heterocyclic ring.
  • the heterocyclic ring is imidazole, pyrrolidine, pyrrolidone, 2-oxopyrrolidine, piperidine, morpholine, or piperazine; each represents a separate embodiment according to this invention.
  • R 2 and R 4 of formula A, I(h) and/or I(m) are joined to form Ring F. In some embodiments, Ring F is absent.
  • Ring F is a substituted or unsubstituted, saturated or unsaturated, 4-8 membered heterocyclic ring.
  • R 2 and R 4 are joined to form pyrrolidine, 1-methylpyrrolidine, pyrrolidin-2-one, pyridine, piperidine, imidazole, pyrimidine, triazole, oxadiazole, pyrazole; each represents a separate embodiment according to this invention.
  • Ring F is unsubstituted, saturated 4-8 membered heterocyclic ring.
  • Ring F is pyrrolidine, morpholine or piperidine; each represents a separate embodiment according to this invention.
  • Ring F is a substituted saturated 4-8 membered heterocyclic ring.
  • Ring F is 1-methylpyrrolidine, 3,3-difluoropyrrolidine, pyrrolidine-3-ol, 3-methoxypyrrolidine, 3-(difluoromethyl)pyrrolidine, or pyrrolidine-3-carbonitrile; each represents a separate embodiment according to this invention.
  • Ring F is a substituted or unsubstituted unsaturated, 4-8 membered heterocyclic ring.
  • Ring F is pyrrolidin-2-one, pyrrolidin-3-one, pyridine, piperidine-2-one, imidazole, pyrimidine, triazole, oxadiazole, or pyrazole; each represents a separate embodiment according to this invention.
  • R 1 is absent.
  • R 3 is absent.
  • R 1 and/or R 3 are absent.
  • R 2 and R 4 of formula A, I(h) and/or I(m) are joined to form substituted or unsubstituted, saturated or unsaturated, 4-8 membered heterocyclic ring.
  • the heterocyclic ring is pyrrolidine, morpholine, 1-methylpyrrolidine, pyrrolidin-2-one, pyrrolidin-3-one, 3,3-difluoropyrrolidine, pyrrolidine-3-ol, 3-methoxypyrrolidine, 3-(difluoromethyl)pyrrolidine, pyrrolidine-3-carbonitrile, pyridine, piperidine, piperidine-2-one, imidazole, pyrimidine, triazole, oxadiazole, or pyrazole; each represents a separate embodiment according to this invention.
  • Ring F is absent.
  • Ring F is a substituted or unsubstituted, saturated or unsaturated, 4-8 membered heterocyclic ring.
  • Ring F is unsubstituted, saturated 4-8 membered heterocyclic ring.
  • Ring F is pyrrolidine, morpholine or piperidine; each represents a separate embodiment according to this invention.
  • Ring F is a substituted saturated 4-8 membered heterocyclic ring.
  • Ring F is 1-methylpyrrolidine, 3,3-difluoropyrrolidine, pyrrolidine-3-ol, 3-methoxypyrrolidine, 3- (difluoromethyl)pyrrolidine, or pyrrolidine-3-carbonitrile; each represents a separate embodiment according to this invention.
  • Ring F is a substituted or unsubstituted unsaturated, 4-8 membered heterocyclic ring.
  • Ring F is pyrrolidin-2-one, pyrrolidin-3-one, pyridine, piperidine-2-one, imidazole, pyrimidine, triazole, oxadiazole, or pyrazole; each represents a separate embodiment according to this invention.
  • Ring F of formula I(h) and/or I(m) is absent.
  • Ring F is a substituted or unsubstituted, saturated or unsaturated, 4-8 membered heterocyclic ring.
  • Ring F is a substituted, saturated, 4-8 membered heterocyclic ring.
  • Ring F is a substituted unsaturated, 4-8 membered heterocyclic ring.
  • Ring F is an unsubstituted, saturated, 4-8 membered heterocyclic ring.
  • Ring F is an unsubstituted, unsaturated, 4-8 membered heterocyclic ring.
  • Ring F is pyrrolidine.
  • Ring F is pyrrolidine-2-one. In some embodiments, Ring F is piperidine. In some embodiments, Ring F is piperazine. In some embodiments, Ring F is morpholine. In some embodiments, Ring F is a pyridinyl. In other embodiments, Ring F is 2-pyridinyl. In other embodiments, Ring F is pyrimidine. In other embodiments, Ring F is imidazole. In other embodiments, Ring F is pyridazine. In other embodiments, Ring F is pyrazine. In other embodiments, Ring F is pyrazole. In other embodiments, Ring F is thiazole. In other embodiments, Ring F is isothiazolyl.
  • Ring F is thiadiazolyl. In other embodiments, Ring F is triazolyl. In other embodiments, Ring F is thiazolyl. In other embodiments, Ring F is oxazolyl. In other embodiments, Ring F is isoxazolyl. In other embodiments, Ring F is pyrrolyl. In other embodiments, Ring F is oxadiazolyl. In other embodiments, Ring F is 1,2,3-, 1,2,4-, 1,2,5- or 1,3,4- oxadiazolyl; each is a separate embodiment according to this invention. In other embodiments, Ring F is oxazolonyl. In other embodiments, Ring F is oxazolidonyl.
  • Ring F is thiazolonyl. In other embodiments, Ring F is isothiazolinonyl. In other embodiments, Ring F is isoxazolidinonyl. In other embodiments, Ring F is imidazolidinonyl. In other embodiments, Ring F is pyrazolonyl. In other embodiments, Ring F is 2H-pyrrol-2-onyl. In other embodiments, Ring F is triazolopyrimidine.
  • Ring F is 3H-[1,2,3]triazolo[4,5-d]pyrimidine, 1H-[1,2,3]triazolo[4,5-d]pyrimidine, [1,2,4]triazolo[4,3-c]pyrimidine, [1,2,4]triazolo[4,3-a]pyrimidine, [1,2,3]triazolo[1,5-a]pyrimidine, [1,2,3]triazolo[1,5-c]pyrimidine, [1,2,4]triazolo[1,5-a]pyrimidine or [1,2,4]triazolo[1,5-c]pyrimidine; each is a separate embodiment according to this invention.
  • R 7 ’ of formula I, II and/or I(a)-I(o) is F, Cl, Br, I, OH, O-R 20 , SH, R 8 -OH, R 8 -SH, -R 8 - O-R 10 , R 8 -(C 3 -C 8 cycloalkyl), R 8 -(3-8 membered heterocyclic ring), CF 3 , CD 3 , OCD 3 , CN, NO 2 , - CH 2 CN, -R 8 CN, NH 2 , NHR, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), R 8 -N(R 10 )(R 11 ), R 9 -R 8 -N(R 10 )(R 11 ), B(OH) 2 , -OC(O)CF 3 , -OCH 2 Ph, NHC(O)-R 10 , NHCO-N(R 10 )(R 11 ),
  • the heterocyclic ring is morpholine, pyran, oxetane, pyrrolidine, 3,3-difluoropyrrolidine, imidazole, pyrazole, triazole, piperazine, piperidine, piperidin-2- one, piperidin-4-ol, dioxazole, 2-oxopyrrolidine; each represents a separate embodiment according to this invention.
  • R 7 ’ is morpholine, pyran, oxetane, pyrrolidine, 3,3- difluoropyrrolidine, imidazole, pyrazole, triazole, piperazine, piperidine, piperidin-2-one, piperidin-4- ol, dioxazole, 2-oxopyrrolidine; each represents a separate embodiment according to this invention.
  • R 7 ’ is further substituted with at least one substitution selected from: F, Cl, Br, I, C 1 -C 5 linear or branched alkyl, OH, alkoxy (e.g., OMe), amide (e.g., C(O)N(R) 2 , C(O)-pyrrolidine, C(O)-piperidine, N(R) 2 NH(R 10 ), N(R 10 )(R 11 ), (e.g., N(CH 3 ) 2 , NH 2 ), CF 3 , aryl, phenyl, heteroaryl, substituted or unsubstituted C 3 -C 8 cycloalkyl (e.g., cyclobutanol), substituted or unsubstituted 3-8 membered heterocyclic ring (e.g.
  • R 7 ’ of formula I, II and/or I(a)-I(o) is H.
  • R 7 ’ is F.
  • R 7 ’ is Cl.
  • R 7 ’ is Br.
  • R 7 ’ is I.
  • R 7 ’ is CF 3 .
  • R 7 ’ is C 1 -C 5 linear or branched, substituted or unsubstituted alkyl. In some embodiments, R 7 ’ is C 1 -C 5 linear or branched unsubstituted alkyl. In some embodiemnts, the alkyl is isopropyl, methyl, ethyl; each represents a separate embodiment according to this invention. In some embodiments, R 7 ’ is C 1 -C 5 linear or branched substituted alkyl. In some embodiments, R 7 ’ is isopropyl. In some embodiments, R 7 ’ is methyl. In some embodiments, R 7 ’ is ethyl.
  • R 7 ’ is C 1 -C 5 linear or branched, or C 3 -C 8 cyclic haloalkyl. In some embodiments, R 7 ’ is C 1 -C 5 linear or branched haloalkyl. In some embodiments, the haloalkyl is CHF 2 . In some embodiments, R 7 ’ is C 3 -C 8 cyclic haloalkyl. In some embodiments, R 7 ’ is substituted or unsubstituted C 3 -C 8 cycloalkyl.
  • R 7 ’ is imidazole. In some embodiments, R 7 ’ is pyrazole. In some embodiments, R 7 ’ is triazole. In some embodiments, R 7 ’ is piperazine. In some embodiments, R 7 ’ is piperidine. In some embodiments, R 7 ’ is piperidin-2-one. In some embodiments, R 7 ’ is piperidin-4- ol. In some embodiments, R 7 ’ is dioxazole. In some embodiments, R 7 ’ is 2-oxopyrrolidine.
  • R 7 and R 7 ’ of formula I, II, and/or I(a)-I(f) are joined to form a 3-8 membered substituted or unsubstituted, saturated, unsaturated or aromatic, carbocyclic or heterocyclic ring including but not limited to: cyclopentyl, cyclohexyl, piperidine, tetrahydrofuran, tetrahydropyran, pyrrolidine; each represents a separate embodiment according to this invention.
  • R 7 and R 7 ’ are joined to form a 5 or 6 membered substituted or unsubstituted, saturated, unsaturated or aromatic, carbocyclic or heterocyclic ring.
  • R 7 and R 7 ’ are joined to form a 5 membered unsubstituted saturated or unsaturated carbocyclic ring. In some embodiments, R 7 and R 7 ’ are joined to form 6 membered unsubstituted saturated or unsaturated carbocyclic ring. In some embodiments, R 7 and R 7 ’ are joined to form a cyclohexyl. In some embodiments, R 7 and R 7 ’ are joined to form a 5 membered substituted saturated or unsaturated carbocyclic ring. In some embodiments, R 7 and R 7 ’ are joined to form a cyclopentyl.
  • R 7 and R 7 ’ are joined to form 6 membered substituted saturated or unsaturated carbocyclic ring. In some embodiments, R 7 and R 7 ’ are joined to form a 6 membered substituted or unsubstituted, aromatic, carbocyclic ring. In some embodiments, R 7 and R 7 ’ are joined to form a 5 or 6 membered substituted or unsubstituted, aromatic, heterocyclic ring. In some embodiments, R 7 and R 7 ’ are joined to form a 5 or 6 membered substituted or unsubstituted, heterocyclic ring.
  • R 7 and R 7 ’ are joined to form a 6 membered substituted or unsubstituted, heterocyclic ring. In some embodiments, R 7 and R 7 ’ are joined to form a piperidine. In some embodiments, R 7 and R 7 ’ are joined to form a tetrahydropyran. In some embodiments, R 7 and R 7 ’ are joined to form a 5 membered substituted or unsubstituted, heterocyclic ring. In some embodiments, R 7 and R 7 ’ are joined to form a pyrrolidine. In some embodiments, R 7 and R 7 ’ are joined to form a tetrahydrofuran.
  • R 7 and R 7 ’ of formula I(c) are different. In some embodiments, R 7 and R 7 ’ of formula I(c) are not H, F, Cl, C 1 -C 5 linear or branched, or C 3 -C 8 cyclic alkoxy , C 1 -C 5 linear or branched haloalkoxy or C 1 -C 5 linear or branched, substituted or unsubstituted alkyl; each represents a separate embodiment according to this invention. [00103] In some embodiments, R 7 ’’ of formula I(i)-I(o) is H.
  • R 7 ’’ of formula I(i)-I(m) is F, Cl, Br, I, OH, O-R 20 , SH, R 8 -OH, R 8 -SH, -R 8 -O-R 10 , R 8 -(C 3 -C 8 cycloalkyl), R 8 -(3-8 membered heterocyclic ring), CF 3 , CD 3 , OCD 3 , CN, NO 2 , -CH 2 CN, -R 8 CN, NH 2 , NHR, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), R 8 -N(R 10 )(R 11 ), R 9 -R 8 -N(R 10 )(R 11 ), B(OH) 2 , -OC(O)CF 3 , -OCH 2 Ph, NHC(O)-R 10 , NHCO- N(R 10 )(R 11 ), COOH, -
  • R 7 ’’ is further substituted with at least one substitution selected from: F, Cl, Br, I, C 1 -C 5 linear or branched alkyl, OH, alkoxy (e.g., OMe), amide (e.g., C(O)N(R) 2 , C(O)-pyrrolidine, C(O)- piperidine, N(R) 2 NH(R 10 ), N(R 10 )(R 11 ), (e.g., N(CH 3 ) 2 , NH 2 ), CF 3 , aryl, phenyl, heteroaryl, substituted or unsubstituted C 3 -C 8 cycloalkyl (e.g., cyclobutanol), substituted or unsubstituted 3-8 membered heterocyclic ring (e.g.
  • R 7 ’’ of formula I(i)-I(o) is H.
  • R 7 ’’ is F.
  • R 7 ’’ is Cl.
  • R 7 ’’ is Br.
  • R 7 ’’ is I.
  • R 7 ’’ is CF 3 .
  • R 7 ’’ is C 1 -C 5 linear or branched, substituted or unsubstituted alkyl. In some embodiments, R 7 ’’ is C 1 -C 5 linear or branched unsubstituted alkyl. In some embodiemnts, the alkyl is isopropyl, methyl, ethyl; each represents a separate embodiment according to this invention. In some embodiments, R 7 ’’ is C 1 -C 5 linear or branched substituted alkyl. In some embodiments, R 7 ’’ is isopropyl. In some embodiments, R 7 ’’ is methyl. In some embodiments, R 7 ’’ is ethyl.
  • R 7 ’’ is C 1 -C 5 linear or branched, or C 3 -C 8 cyclic alkoxy optionally wherein at least one methylene group (CH 2 ) in the alkoxy is replaced with an oxygen atom.
  • R 7 ’’ is C 1 -C 5 linear or branched alkoxy.
  • R 7 ’’ is methoxy.
  • R 7 ’’ is C 1 -C 5 linear or branched, or C 3 -C 8 cyclic haloalkyl.
  • R 7 ’’ is C 1 -C 5 linear or branched haloalkyl.
  • the haloalkyl is CHF 2 .
  • R 7 ’’ is C 3 -C 8 cyclic haloalkyl.
  • R 7 ’’ is substituted or unsubstituted C 3 -C 8 cycloalkyl.
  • the cycloalkyl is cyclopropyl, cyclpbutyl, cyclopentyl, cyclohexyl, or cycloheptyl; each represents a separate embodiment according to this invention.
  • the cycloalkyl is cyclopropyl.
  • the cycloalkyl is cyclohexyl.
  • R 7 ’’ is a substituted or unsubstituted 3-8 membered heterocyclic ring. In some embodiments, R 7 ’’ is morpholine. In some embodiments, R 7 ’’ is pyran. In some embodiments, R 7 ’’ is oxetane. In some embodiments, R 7 ’’ is pyrrolidine. In some embodiments, R 7 ’’’’ is 3,3- difluoropyrrolidine. In some embodiments, R 7 ’’ is imidazole. In some embodiments, R 7 ’’’’ is pyrazole. In some embodiments, R 7 ’’ is triazole. In some embodiments, R 7 ’’ is piperazine.
  • R 7 ’’ is piperidine. In some embodiments, R 7 ’’ is piperidin-2-one. In some embodiments, R 7 ’’ is piperidin-4-ol. In some embodiments, R 7 ’’ is dioxazole. In some embodiments, R 7 ’’ is 2-oxopyrrolidine.
  • R 7 ’ and R 7 ’’ of formula I(j)-I(o) are joined to form a 3-8 membered substituted or unsubstituted, saturated, unsaturated or aromatic, carbocyclic or heterocyclic ring including but not limited to: cyclopentyl, cyclohexyl, piperidine, tetrahydrofuran, tetrahydropyran, pyrrolidine; each represents a separate embodiment according to this invention.
  • R 7 ’ and R 7 ’’ are joined to form a 5 or 6 membered substituted or unsubstituted, saturated, unsaturated or aromatic, carbocyclic or heterocyclic ring.
  • R 7 ’ and R 7 ’’ are joined to form a 5 membered unsubstituted saturated or unsaturated carbocyclic ring. In some embodiments, R 7 ’ and R 7 ’’ are joined to form 6 membered unsubstituted saturated or unsaturated carbocyclic ring. In some embodiments, R 7 ’ and R 7 ’’ are joined to form a cyclohexyl. In some embodiments, R 7 ’ and R 7 ’’ are joined to form a 5 membered substituted saturated or unsaturated carbocyclic ring. In some embodiments, R 7 ’ and R 7 ’’ are joined to form a cyclopentyl.
  • R 7 ’ and R 7 ’’ are joined to form 6 membered substituted saturated or unsaturated carbocyclic ring. In some embodiments, R 7 ’ and R 7 ’’ are joined to form a 6 membered substituted or unsubstituted, aromatic, carbocyclic ring. In some embodiments, R 7 ’ and R 7 ’’ are joined to form a 5 or 6 membered substituted or unsubstituted, aromatic, heterocyclic ring. In some embodiments, R 7 ’ and R 7 ’’ are joined to form a 5 or 6 membered substituted or unsubstituted, heterocyclic ring.
  • R 7 ’ and R 7 ’’ are joined to form a 6 membered substituted or unsubstituted, heterocyclic ring. In some embodiments, R 7 ’ and R 7 ’’ are joined to form a piperidine. In some embodiments, R 7 ’ and R 7 ’’ are joined to form a tetrahydropyran. In some embodiments, R 7 ’ and R 7 ’’ are joined to form a 5 membered substituted or unsubstituted, heterocyclic ring. In some embodiments, R 7 ’ and R 7 ’’ are joined to form a pyrrolidine.
  • R 7 ’ and R 7 ’’ are joined to form a tetrahydrofuran.
  • R 7 ’ and R 7 ’’ of formula I(c) and/or I(i)-I(o) are different.
  • R 7 and R 7 ’ of formula I(c) and/or I(i)-I(n) are not H, F, Cl, C 1 -C 5 linear or branched, or C 3 -C 8 cyclic alkoxy , C 1 -C 5 linear or branched haloalkoxy or C 1 -C 5 linear or branched, substituted or unsubstituted alkyl; each represents a separate embodiment according to this invention.
  • R 7 ’’’ of formula I(i) is H.
  • R 7 ’’’ of formula I(i) is F, Cl, Br, I, OH, O-R 20 , SH, R 8 -OH, R 8 -SH, -R 8 -O-R 10 , R 8 -(C 3 -C 8 cycloalkyl), R 8 -(3-8 membered heterocyclic ring), CF 3 , CD 3 , OCD 3 , CN, NO 2 , -CH 2 CN, -R 8 CN, NH 2 , NHR, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), R 8 -N(R 10 )(R 11 ), R 9 -R 8 -N(R 10 )(R 11 ), B(OH) 2 , -OC(O)CF 3 , -OCH 2 Ph, NHC(O)-R 10 ,
  • R 7 ’’’ is further substituted with at least one substitution selected from: F, Cl, Br, I, C 1 -C 5 linear or branched alkyl, OH, alkoxy (e.g., OMe), amide (e.g., C(O)N(R) 2 , C(O)-pyrrolidine, C(O)- piperidine, N(R) 2 NH(R 10 ), N(R 10 )(R 11 ), (e.g., N(CH 3 ) 2 , NH 2 ), CF 3 , aryl, phenyl, heteroaryl, substituted or unsubstituted C 3 -C 8 cycloalkyl (e.g., cyclobutanol), substituted or unsubstituted 3-8 membered heterocyclic ring (e.g.
  • R 7 ’’’ of formula I(i) is H.
  • R 7 ’’’ is F.
  • R 7 ’’’ is Cl.
  • R 7 ’’’ is Br.
  • R 7 ’’’ is I.
  • R 7 ’’’ is CF 3 .
  • R 7 ’’’ is C 1 -C 5 linear or branched, substituted or unsubstituted alkyl. In some embodiments, R 7 ’’’ is C 1 -C 5 linear or branched unsubstituted alkyl. In some embodiemnts, the alkyl is isopropyl, methyl, ethyl; each represents a separate embodiment according to this invention. In some embodiments, R 7 ’’’’ is C 1 -C 5 linear or branched substituted alkyl. In some embodiments, R 7 ’’’ is isopropyl. In some embodiments, R 7 ’’’ is methyl. In some embodiments, R 7 ’’’ is ethyl.
  • R 7 ’’’ is C 1 -C 5 linear or branched, or C 3 -C 8 cyclic alkoxy optionally wherein at least one methylene group (CH 2 ) in the alkoxy is replaced with an oxygen atom.
  • R 7 ’’’ is C 1 -C 5 linear or branched alkoxy.
  • R 7 ’’’ is methoxy.
  • R 7 ’’’ is C 1 -C 5 linear or branched, or C 3 -C 8 cyclic haloalkyl.
  • R 7 ’’’ is C 1 -C 5 linear or branched haloalkyl.
  • the haloalkyl is CHF 2 .
  • R 7 ’’’ is C 3 -C 8 cyclic haloalkyl.
  • R 7 ’’’ is substituted or unsubstituted C 3 -C 8 cycloalkyl.
  • the cycloalkyl is cyclopropyl, cyclpbutyl, cyclopentyl, cyclohexyl, or cycloheptyl; each represents a separate embodiment according to this invention.
  • R 7 ’’’ is a substituted or unsubstituted 3-8 membered heterocyclic ring.
  • R 7 ’’’ is morpholine. In some embodiments, R 7 ’’’ is pyran. In some embodiments, R 7 ’’’ is oxetane. In some embodiments, R 7 ’’’ is pyrrolidine. In some embodiments, R 7 ’’’ is 3,3- difluoropyrrolidine. In some embodiments, R 7 ’’’ is imidazole. In some embodiments, R 7 ’’’ is pyrazole. In some embodiments, R 7 ’’’ is triazole. In some embodiments, R 7 ’’’’ is piperazine. In some embodiments, R 7 ’’’ is piperidine.
  • R 7 ’’’ is piperidin-2-one. In some embodiments, R 7 ’’’’ is piperidin-4-ol. In some embodiments, R 7 ’’’ is dioxazole. In some embodiments, R 7 ’’’ is 2- oxopyrrolidine. [00109] In some embodiments, R 7 ’’’’ of formula I(i) is H.
  • R 7 ’’’ of formula I(i) is F, Cl, Br, I, OH, O-R 20 , SH, R 8 -OH, R 8 -SH, -R 8 -O-R 10 , R 8 -(C 3 -C 8 cycloalkyl), R 8 -(3-8 membered heterocyclic ring), CF 3 , CD 3 , OCD 3 , CN, NO 2 , -CH 2 CN, -R 8 CN, NH 2 , NHR, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), R 8 -N(R 10 )(R 11 ), R 9 -R 8 -N(R 10 )(R 11 ), B(OH) 2 , -OC(O)CF 3 , -OCH 2 Ph, NHC(O)-R 10 , NHCO- N(R 10 )(R 11 ), COOH, -C(O)
  • R 7 ’’’’ is further substituted with at least one substitution selected from: F, Cl, Br, I, C 1 - C 5 linear or branched alkyl, OH, alkoxy (e.g., OMe), amide (e.g., C(O)N(R) 2 , C(O)-pyrrolidine, C(O)- piperidine, N(R) 2 NH(R 10 ), N(R 10 )(R 11 ), (e.g., N(CH 3 ) 2 , NH 2 ), CF 3 , aryl, phenyl, heteroaryl, substituted or unsubstituted C 3 -C 8 cycloalkyl (e.g., cyclobutanol), substituted or unsubstituted 3-8 membered heterocyclic ring (e.g.
  • R 7 ’’’’ of formula I(i) is H.
  • R 7 ’’’’ is F.
  • R 7 ’’’’ is Cl.
  • R 7 ’’’’ is Br.
  • R 7 ’’’’ is I.
  • R 7 ’’’’ is CF 3 .
  • R 7 ’’’’ is C 1 -C 5 linear or branched, substituted or unsubstituted alkyl. In some embodiments, R 7 ’’’ is C 1 -C 5 linear or branched unsubstituted alkyl. In some embodiments, the alkyl is isopropyl, methyl, ethyl; each represents a separate embodiment according to this invention. In some embodiments, R 7 ’’’’’ is C 1 -C 5 linear or branched substituted alkyl. In some embodiments, R 7 ’’’’ is isopropyl. I’n some embodiments, R 7 ’’’’ is methyl.
  • R 7 ’’’’ is ethyl. In some embodiments, R 7 ’’’’ is C 1 -C 5 linear or branched, or C 3 -C 8 cyclic alkoxy optionally wherein at least one methylene group (CH 2 ) in the alkoxy is replaced with an oxygen atom. In some embodiments, R 7 ’’’’ is C 1 -C 5 linear or branched alkoxy. In some embodiments, R 7 ’’ is methoxy. In some embodiments, R 7 ’’’’ is C 1 -C 5 linear or branched, or C 3 -C 8 cyclic haloalkyl.
  • R 7 ’’’ is C 1 -C 5 linear or branched haloalkyl.
  • the haloalkyl is CHF 2 .
  • R 7 ’’’ is C 3 -C 8 cyclic haloalkyl.
  • R 7 ’’’ is substituted or unsubstituted C 3 -C 8 cycloalkyl.
  • the cycloalkyl is cyclopropyl, cyclpbutyl, cyclopentyl, cyclohexyl, or cycloheptyl; each represents a separate embodiment according to this invention.
  • R 7 ’’’’ is a substituted or unsubstituted 3-8 membered heterocyclic ring. In some embodiments, R 7 ’’’’ is morpholine. In some embodiments, R 7 ’’’’ is pyran. In some embodiments, R 7 ’’’’ is oxetane. In some embodiments, R 7 ’’’’ is pyrrolidine. In some embodiments, R 7 ’’’’’ is 3,3-difluoropyrrolidine. In some embodiments, R 7 ’’’’ is imidazole. In some embodiments, R 7 ’’’’ is pyrazole. In some embodiments, R 7 ’’’’ is triazole.
  • R 7 ’’’’ is piperazine. In some embodiments, R 7 ’’’’ is piperidine. In some embodiments, R 7 ’’’’ is piperidin-2-one. In some embodiments, R 7 ’’’’ is piperidin-4-ol. In some embodiments, R 7 ’’’’ is dioxazole. In some embodiments, R 7 ’’’’ is 2-oxopyrrolidine. [00111] In some embodiments, R 7 ’ and R 7 ’’ of formula I(i) are joined to form a 3-8 membered substituted or unsubstituted, saturated, unsaturated or aromatic, carbocyclic or heterocyclic ring.
  • R 7 ’ and R 7 ’’ are joined to form a 5 membered unsubstituted saturated or unsaturated carbocyclic ring. In some embodiments, R 7 ’ and R 7 ’’ are joined to form a cyclopentane. In some embodiments, R 7 ’ and R 7 ’’ are joined to form 6 membered unsubstituted saturated or unsaturated carbocyclic ring. In some embodiments, R 7 ’ and R 7 ’’ are joined to form a cyclohexane. In some embodiments, R 7 ’ and R 7 ’’ are joined to form a 5 membered substituted saturated or unsaturated carbocyclic ring.
  • R 7 ’ and R 7 ’’ are joined to form 6 membered substituted saturated or unsaturated carbocyclic ring. In some embodiments, R 7 ’ and R 7 ’’ are joined to form a 6 membered substituted or unsubstituted, aromatic, carbocyclic ring. In some embodiments, R 7 ’ and R 7 ’’ are joined to form a 5 or 6 membered substituted or unsubstituted, aromatic, heterocyclic ring. In some embodiments, R 7 ’ and R 7 ’’ are joined to form a 5 or 6 membered substituted or unsubstituted, heterocyclic ring.
  • R 7 ’ and R 7 ’’ are joined to form a 6 membered substituted or unsubstituted, heterocyclic ring. In some embodiments, R 7 ’ and R 7 ’’ are joined to form a piperidine. In some embodiments, R 7 ’ and R 7 ’’ are joined to form a tetrahydropyran. In some embodiments, R 7 ’ and R 7 ’’ are joined to form a 5 membered substituted or unsubstituted, heterocyclic ring. In some embodiments, R 7 ’ and R 7 ’’ are joined to form a tetrahydrofuran.
  • R 7 ’ and R 7 ’’ are joined to form a pyrrolidine.
  • R 7 ’ and R 7 ’’ of formula I(i) are different.
  • R 7 ’ and R 7 ’’ of formula I(i) are not H, F, Cl, C 1 -C 5 linear or branched, or C 3 -C 8 cyclic alkoxy, C 1 -C 5 linear or branched haloalkoxy or C 1 -C 5 linear or branched, substituted or unsubstituted alkyl; each represents a separate embodiment according to this invention.
  • R 7 ’’ and R 7 of formula I(i) are joined to form a 3-8 membered substituted or unsubstituted, saturated, unsaturated or aromatic, carbocyclic or heterocyclic ring. In some embodiments, R 7 ’’ and R 7 are joined to form a 5 membered unsubstituted saturated or unsaturated carbocyclic ring. In some embodiments, R 7 ’’ and R 7 are joined to form a cyclopentane. In some embodiments, R 7 ’’ and R 7 are joined to form 6 membered unsubstituted saturated or unsaturated carbocyclic ring.
  • R 7 ’’ and R 7 are joined to form a cyclohexane. In some embodiments, R 7 ’’ and R 7 are joined to form a 5 membered substituted saturated or unsaturated carbocyclic ring. In some embodiments, R 7 ’’ and R 7 are joined to form 6 membered substituted saturated or unsaturated carbocyclic ring. In some embodiments, R 7 ’ and R 7 ’’ are joined to form a 6 membered substituted or unsubstituted, aromatic, carbocyclic ring. In some embodiments, R 7 ’’ and R 7 are joined to form a 5 or 6 membered substituted or unsubstituted, aromatic, heterocyclic ring.
  • R 7 ’’ and R 7 are joined to form a 5 or 6 membered substituted or unsubstituted, heterocyclic ring. In some embodiments, R 7 ’’ and R 7 are joined to form a 6 membered substituted or unsubstituted, heterocyclic ring. In some embodiments, R 7 ’’ and R 7 are joined to form a piperidine. In some embodiments, R 7 ’’ and R 7 are joined to form a tetrahydropyran. In some embodiments, R 7 ’’ and R 7 are joined to form a 5 membered substituted or unsubstituted, heterocyclic ring.
  • R 7 ’’ and R 7 are joined to form a tetrahydrofuran. In some embodiments, R 7 ’’ and R 7 are joined to form a pyrrolidine. [00114] In some embodiments, R 7 ’’ and R 7 of formula I(i) are different. In some embodiments, R 7 ’’ and R 7 of formula I(i) are not H, F, Cl, C 1 -C 5 linear or branched, or C 3 -C 8 cyclic alkoxy , C 1 -C 5 linear or branched haloalkoxy or C 1 -C 5 linear or branched, substituted or unsubstituted alkyl; each represents a separate embodiment according to this invention.
  • R 7 and R 7 ’’’ of formula I(i) are joined to form a 3-8 membered substituted or unsubstituted, saturated, unsaturated or aromatic, carbocyclic or heterocyclic ring. In some embodiments, R 7 and R 7 ’’’ are joined to form a 5 membered unsubstituted saturated or unsaturated carbocyclic ring. In some embodiments, R 7 and R 7 ’’’ are joined to form 6 membered unsubstituted saturated or unsaturated carbocyclic ring. In some embodiments, R 7 and R 7 ’’’ are joined to form a 5 membered substituted saturated or unsaturated carbocyclic ring.
  • R 7 and R 7 ’’’ are joined to form 6 membered substituted saturated or unsaturated carbocyclic ring. In some embodiments, R 7 and R 7 ’’’ are joined to form a 6 membered substituted or unsubstituted, aromatic, carbocyclic ring. In some embodiments, R 7 and R 7 ’’ are joined to form a 5 or 6 membered substituted or unsubstituted, aromatic, heterocyclic ring. In some embodiments, R 7 and R 7 ’’’ are joined to form a 5 or 6 membered substituted or unsubstituted, heterocyclic ring.
  • R 7 and R 7 ’’’ are joined to form a cyclopentane. In some embodiments, R 7 and R 7 ’’’ are joined to form a cyclohexane. [00116] In some embodiments, R 7 and R 7 ’’’ of formula I(i) are different. In some embodiments, R 7 and R 7 ’’’ of formula I(i) are not H, F, Cl, C 1 -C 5 linear or branched, or C 3 -C 8 cyclic alkoxy , C 1 -C 5 linear or branched haloalkoxy or C 1 -C 5 linear or branched, substituted or unsubstituted alkyl; each represents a separate embodiment according to this invention.
  • R 7 ’’’ and R 7 ’’’’ of formula I(i) are joined to form a 3-8 membered substituted or unsubstituted, saturated, unsaturated or aromatic, carbocyclic or heterocyclic ring. In some embodiments, R 7 ’’’ and R 7 ’’’’ are joined to form a 5 membered unsubstituted saturated or unsaturated carbocyclic ring. In some embodiments, R 7 ’’’ and R 7 ’’’’ are joined to form 6 membered unsubstituted saturated or unsaturated carbocyclic ring.
  • R 7 ’’’ and R 7 ’’’’ are joined to form a 5 membered substituted saturated or unsaturated carbocyclic ring. In some embodiments, R 7 ’’’ and R 7 ’’’’ are joined to form 6 membered substituted saturated or unsaturated carbocyclic ring. In some embodiments, R 7 ’’’ and R 7 ’’’ are joined to form a 6 membered substituted or unsubstituted, aromatic, carbocyclic ring. In some embodiments, R 7 ’’’ and R 7 ’’’’ are joined to form a 5 or 6 membered substituted or unsubstituted, aromatic, heterocyclic ring.
  • R 7 ’’’ and R 7 ’’’’ are joined to form a 5 or 6 membered substituted or unsubstituted, heterocyclic ring. In some embodiments, R 7 ’’’ and R 7 ’’’ are joined to form a 6 membered substituted or unsubstituted, heterocyclic ring. In some embodiments, R 7 ’’’ and R 7 ’’’ are joined to form a piperidine. In some embodiments, R 7 ’’’ and R 7 ’’’’ are joined to form a tetrahydrofuran. In some embodiments, R 7 ’’’ and R 7 ’’’’ are joined to form a tetrahydropyran.
  • R 7 ’’’ and R 7 ’’’’ are joined to form a 5 membered substituted or unsubstituted, heterocyclic ring. In some embodiments, R 7 ’’’ and R 7 ’’’’ are joined to form a pyrrolidine. In some embodiments, R 7 ’’’ and R 7 ’’’’ are joined to form a cyclopentane. In some embodiments, R 7 ’’’’ and R 7 ’’’’’ are joined to form a cyclohexane. [00118] In some embodiments, R 7 ’’’ and R 7 ’’’’’ of formula I(i) are different.
  • R 7 ’’’ and R 7 ’’’ of formula I(i) are not H, F, Cl, C 1 -C 5 linear or branched, or C 3 -C 8 cyclic alkoxy , C 1 - C 5 linear or branched haloalkoxy or C 1 -C 5 linear or branched, substituted or unsubstituted alkyl; each represents a separate embodiment according to this invention. [00119] In some embodiments, at least two of R 7 , R 7 ’, R 7 ’’, R 7 ’’’ and R 7 ’’’’’ are not H.
  • R 30 of formula I, II and/or I(a)-I(o) is H, R 20 , F, Cl, Br, I, OH, SH, alkoxy, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), CF 3 , CN, NO 2 , C 1 -C 5 linear or branched, substituted or unsubstituted alkyl, methyl, ethyl, CH 2 -CH 2 -O-CH 2 -CH 2 -O-CH 3 , CH 2 -O-CH 2 -CH 2 -O-CH 3 , C 1 -C 5 linear or branched alkoxy, C 1 -C 5 linear or branched haloalkyl, CHF 2 , CF 3 , CF 2 CH
  • R 30 is further substituted with at least one substitution selected from: F, Cl, Br, I, C 1 -C 5 linear or branched alkyl, OH, alkoxy (e.g., OMe), amide (e.g., C(O)N(R) 2 , C(O)-pyrrolidine, C(O)-piperidine, N(R) 2 NH(R 10 ), N(R 10 )(R 11 ), (e.g., N(CH 3 ) 2 , NH 2 ), CF 3 , aryl, phenyl, heteroaryl, substituted or unsubstituted C 3 -C 8 cycloalkyl (e.g., cyclobutanol), substituted or unsubstituted 3-8 membered heterocyclic ring (e.g.
  • R 30 is H. In some embodiments, R 30 is alkyl. In some embodiments, R 30 is methyl. In some embodiments, R 30 is R 20 .
  • R of formula I, II and/or I(a)-I(o) is H, F, Cl, Br, I, OH, SH, alkoxy, NH(R 10 ), N(R 10 )(R 11 ), CF 3 , CN, NO 2 , COOH, C 1 -C 5 linear or branched, substituted or unsubstituted alkyl, C 1 -C 5 linear or branched alkoxy, C 1 -C 5 linear or branched haloalkyl, R 8 -aryl, -R 8 -O-R 8 -O-R 10 , - R 8 -O-R 10 , -R 8 -R 10 , substituted or unsubstituted aryl, or substituted or unsubstituted heteroaryl; each represents a separate embodiment according to this invention.
  • R is further substituted with at least one substitution selected from: F, Cl, Br, I, C 1 -C 5 linear or branched alkyl, OH, alkoxy (e.g., OMe), amide (e.g., C(O)N(R) 2 , C(O)-pyrrolidine, C(O)-piperidine, N(R) 2 NH(R 10 ), N(R 10 )(R 11 ), (e.g., N(CH 3 ) 2 , NH 2 ), CF 3 , aryl, phenyl, heteroaryl, substituted or unsubstituted C 3 -C 8 cycloalkyl (e.g., cyclobutanol), substituted or unsubstituted 3-8 membered heterocyclic ring (e.g.
  • R is H.
  • R is NH(R 10 ).
  • R is NH-CH 2 -cyclopropyl.
  • R is C 1 -C 5 linear or branched, substituted or unsubstituted alkyl.
  • R is methyl.
  • R is ethyl.
  • R is propyl.
  • R is isopropyl. In some embodiments, R is butyl. In some embodiments, R is substituted alkyl. In some embodiments, R is CH 2 -OH. In some embodiments, R is CH 2 -CH 2 -OH. In some embodiments, R is C3- C8 substituted or unsubstituted cycloalkyl. In some embodiments, R is cyclopropyl. In some embodiments, R is C 1 -C 5 linear or branched alkoxy. In some embodiments, R is methoxy. In some embodiments, R is ethoxy. In some embodiments, R is propoxy. In some embodiments, R is isopropoxy. In some embodiments, R is COOH.
  • R is R 8 -O-R 10 . In some embodiments, R is CH 2 -OH. In some embodiments, R is CH 2 -CH 2 -OH. [00122] In various embodiments, each R 8 of compound of formula I, II and/or I(a)-I(o) is independently CH 2 . In some embodiments, R 8 is CH 2 CH 2 . In some embodiments, R 8 is CH 2 CH 2 CH 2 . In some embodiments, R 8 is CH 2 CH 2 CH 2 CH 2 . In some embodiments, R 8 is CH 2 CH 2 CH 2 CH 2 . [00123] In some embodiments, p of formula I, II and/or I(a)-I(o) is 1. In other embodiments, p is 2. In other embodiments, p is 3. In some embodiments, p is 4.
  • R 10 of formula I, II and/or I(a)-I(o) is H, C 1 -C 5 substituted or unsubstituted linear or branched alkyl (e.g., methyl, ethyl, CH 2 -cyclopropyl, CH 2 -CH 2 -O-CH 3 ; each represents a separate embodiment according to this invention), C 1 -C 5 substituted or unsubstituted linear or branched haloalky, CH 2 CF 3 , C 1 -C 5 linear or branched alkoxy (e.g., O-CH 3 ), R 20 , C(O)R, or S(O) 2 R; each represents a separate embodiment according to this invention.
  • C 1 -C 5 substituted or unsubstituted linear or branched alkyl e.g., methyl, ethyl, CH 2 -cyclopropyl, CH 2 -CH 2 -O-CH 3 ; each represents a separate embodiment according
  • R 10 is H. In some embodiments, R 10 is C 1 -C 5 substituted or unsubstituted linear or branched alkyl. In some embodiments, R 10 is C 1 -C 5 unsubstituted linear or branched alkyl. In other embodiments, R 10 is CH 3 . In other embodiments, R 10 is CH 2 CH 3. In other embodiments, R 10 is CH 2 CH 2 CH 3 . In some embodiments, R 10 is is isopropyl. In some embodiments, R 10 is butyl. In some embodiments, R 10 is isobutyl. In some embodiments, R 10 is t-butyl. In some embodiments, R 10 is pentyl.
  • R 10 is isopentyl. In some embodiments, R 10 is neopentyl. In some embodiments, R 10 is benzyl. In some embodiments, R 10 is C 1 -C 5 substituted linear or branched alkyl. In other embodiments, R 10 is CH 2 -CH 2 -O-CH 3 . In other embodiments, R 10 is CH 2 CF 3 . In other embodiments, R 10 is C 1 -C 5 substituted or unsubstituted linear or branched haloalkyl. In other embodiments, R 10 is C 1 -C 5 linear or branched alkoxy. In other embodiments, R 10 is O-CH 3 . In other embodiments, R 10 is R 20 .
  • R 10 is C(O)R. In other embodiments, R 10 is S(O) 2 R. In some embodiments, R 10 is further substituted with at lest one substitution selected from: F, Cl, Br, I, C 1 -C 5 linear or branched alkyl, OH, alkoxy (e.g., OMe), amide (e.g., C(O)N(R) 2 , C(O)-pyrrolidine, C(O)-piperidine, N(R) 2 NH(R 10 ), N(R 10 )(R 11 ), (e.g., N(CH 3 ) 2 , NH 2 ), CF 3 , aryl, phenyl, heteroaryl, substituted or unsubstituted C 3 -C 8 cycloalkyl (e.g., cyclobutanol), substituted or unsubstituted 3-8 membered heterocyclic ring (e.g.
  • pyran oxetane, piperidine, pyrazole, methyl-pyrrazole, triazole, imidazole), halophenyl, (benzyloxy)phenyl, CN and NO 2 ; each represents a separate embodiment according to this invention.
  • R 11 of formula I, II and/or I(a)-I(o) is H, C 1 -C 5 substituted or unsubstituted linear or branched alkyl (e.g., methyl, ethyl, CH 2 -CH 2 -O-CH 3 , CH 2 CF 3 , C 1 -C 5 linear or branched alkoxy (e.g., O-CH 3 ), C(O)R, or S(O) 2 R; each represents a separate embodiment according to this invention.
  • R 11 is H.
  • R 11 is C 1 -C 5 substituted or unsubstituted linear or branched alkyl.
  • R 11 is C 1 -C 5 unsubstituted linear or branched alkyl. In other embodiments, R 11 is CH 3 . In other embodiments, R 11 is CH 2 CH 3 . In other embodiments, R 11 is CH 2 CH 2 CH 3 . In some embodiments, R 11 is isopropyl. In some embodiments, R 11 is butyl. In some embodiments, R 11 is isobutyl. In some embodiments, R 11 is t-butyl. In some embodiments, R 11 is pentyl. In some embodiments, R 11 is isopentyl. In some embodiments, R 11 is neopentyl. In some embodiments, R 11 is benzyl.
  • R 11 is C 1 -C 5 substituted linear or branched alkyl. In other embodiments, R 11 is CH 2 -CH 2 -O-CH 3 . In other embodiments, R 11 is CH 2 CF 3 . In other embodiments, R 11 is C 1 -C 5 substituted or unsubstituted linear or branched haloalkyl. In other embodiments, R 11 is C 1 -C 5 linear or branched alkoxy. In other embodiments, R 11 is O-CH 3 . In other embodiments, R 11 is R 20 . In other embodiments, R 11 is C(O)R. In other embodiments, R 11 is S(O) 2 R.
  • R 11 is further substituted with at lest one substitution selected from: F, Cl, Br, I, C 1 - C 5 linear or branched alkyl, OH, alkoxy (e.g., OMe), amide (e.g., C(O)N(R) 2 , C(O)-pyrrolidine, C(O)- piperidine, N(R) 2 NH(R 10 ), N(R 10 )(R 11 ), (e.g., N(CH 3 ) 2 , NH 2 ), CF 3 , aryl, phenyl, heteroaryl, substituted or unsubstituted C 3 -C 8 cycloalkyl (e.g., cyclobutanol), substituted or unsubstituted 3-8 membered heterocyclic ring (e.g.
  • R 10 and R 11 of formula I, II and/or I(a)-I(o) are joined to form a substituted or unsubstituted 3-8 membered heterocyclic ring.
  • R 10 and R 11 are joined to form a piperazine ring.
  • R 10 and R 11 are joined to form a piperidine ring.
  • substitutions include: F, Cl, Br, I, C 1 -C 5 linear or branched alkyl, OH, alkoxy , OMe, amide , C(O)N(R) 2 , C(O)-pyrrolidine, C(O)-piperidine, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), N(CH 3 ) 2 , NH 2 , CF 3 , aryl, phenyl, heteroaryl, substituted or unsubstituted C 3 -C 8 cycloalkyl , cyclobutanol, substituted or unsubstituted 3-8 membered heterocyclic ring pyran, oxetane, piperidine, pyrazole, methyl-pyrrazole, triazole, imidazole, halophenyl, (benzyloxy)phenyl, CN, and NO 2 ; each represents a separate embodiment according to
  • n of formula I, II, I(a)-I(h) and/or I(j)-I(o) is an integer between 0 and 4. In some embodiments, n of formula I(c) is an integer between 1 and 4. In some embodiments, n of formula I, II, I(a)-I(h) and/or I(j)-I(n) is 0. In some embodiments, n of formula I, II, I(a)-I(h) and/or I(j)-I(n) is 1. In some embodiments, n of formula I, II, I(a)-I(h) and/or I(j)-I(n) is 2.
  • n of formula I, II, I(a)-I(h) and/or I(j)-I(n) is 3. In some embodiments, n of formula I, II, I(a)-I(h) and/or I(j)-I(n) is 4. In some embodiments, n of formula I, II, I(a)-I(h) and/or I(j)-I(n) is 1 or 2. [00130] In some embodiments, A’ of formula I(f) is a 3-8 membered single or fused saturated, unsaturated or aromatic heterocyclic ring. In some embodiments, A’ is a 3-8 membered single heterocyclic ring.
  • A’ is a fused 4-10 membered heterocyclic ring. In some embodiments, A’ is a single aromatic 3-8 membered heterocyclic ring. In some embodiments, A’ is a fused aromatic 3-10 membered heterocyclic ring. In some embodiments, A’ is a saturated 3-8 membered single heterocyclic ring. In some embodiments, A’ is piperidine. In some embodiments, A’ is pyrrolidine. In some embodiments, A’ is piperazine. In some embodiments, A’ is morpholine. In some embodiments, A’ is a pyridinyl. In other embodiments, A’ is 2-pyridinyl. In other embodiments, A’ is 3-pyridinyl.
  • A’ is 4-pyridinyl. In other embodiments, A’ is pyrimidine. In other embodiments, A’ is pyridazine. In other embodiments, A’ is pyrazine. In other embodiments, A’ is pyrazole. In other embodiments, A’ is benzothiazolyl. In other embodiments, A’ is benzimidazolyl. In other embodiments, A’ is quinolinyl. In other embodiments, A’ is isoquinolinyl. In other embodiments, A’ is indolyl. In other embodiments, A’ is indenyl. In other embodiments, A’ is benzofuran-2(3H)-one.
  • A’ is benzo[d][1,3]dioxole. In other embodiments, A’ is tetrahydrothiophene1,1- dioxide. In other embodiments, A’ is thiazole. In other embodiments, A’ is benzimidazole. In others embodiment, A’ is piperidine. In other embodiments, A’ is imidazole. In other embodiments, A’ is thiophene. In other embodiments, A’ is isoquinoline. In other embodiments, A’ is indole. In other embodiments, A’ is 1,3-dihydroisobenzofuran. In other embodiments, A’ is benzofuran.
  • A’ is tetrahydro-2H-pyran. In other embodiments, A’ is isothiazolyl. In other embodiments, A’ is thiadiazolyl. In other embodiments, A’ is triazolyl. In other embodiments, A’ is thiazolyl. In other embodiments, A’ is oxazolyl. In other embodiments, A’ is isoxazolyl. In other embodiments, A’ is pyrrolyl. In other embodiments, A’ is furanyl. In other embodiments, A’ is oxadiazolyl.
  • A’ is 1,2,3-, 1,2,4-, 1,2,5- or 1,3,4- oxadiazolyl; each is a separate embodiment according to this invention.
  • A’ is tetrahydrofuranyl.
  • A’ is oxazolonyl.
  • A’ is oxazolidonyl.
  • A’ is thiazolonyl.
  • A’ is isothiazolinonyl.
  • A’ is isoxazolidinonyl.
  • A’ is imidazolidinonyl.
  • A’ is pyrazolonyl.
  • A’ is 2H-pyrrol-2-onyl. In other embodiments, A’ is furanonyl. In other embodiments, A’ is thiophenonyl. In other embodiments, A’ is thiane 1,1 dioxide. In other embodiments, A’ is triazolopyrimidine.
  • A’ is 3H-[1,2,3]triazolo[4,5-d]pyrimidine, 1H- [1,2,3]triazolo[4,5-d]pyrimidine, [1,2,4]triazolo[4,3-c]pyrimidine, [1,2,4]triazolo[4,3-a]pyrimidine, [1,2,3]triazolo[1,5-a]pyrimidine, [1,2,3]triazolo[1,5-c]pyrimidine, [1,2,4]triazolo[1,5-a]pyrimidine or [1,2,4]triazolo[1,5-c]pyrimidine; each is a separate embodiment according to this invention.
  • A’ is 6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine. In other embodiments, A’ is 1,2,3,4- tetrahydronaphthalene. In other embodiments, A’ is chroman. In other embodiments, A’ is isochroman. In other embodiments, A’ is 1,2,3,4-tetrahydroquinoline. In other embodiments, A’ is 1,2,3,4- tetrahydroisoquinoline. In other embodiments, A’ is 2,3-dihydro-1H-indene. In other embodiments, A’ is 2,3-dihydrobenzofuran.
  • A’ is 1,3-dihydroisobenzofuran. In other embodiments, A’ is isoindoline. In other embodiments, A’ is indoline. In some embodiments, A’ of formula I(f) is not a phenyl.
  • R 100 of formula I(g) is H, C 1 -C 5 substituted or unsubstituted linear or branched alkyl (e.g., methyl, ethyl), R 8 -OH (e.g., (CH 2 ) 2 -OH), -R 8 -O-R 10 (e.g., (CH 2 ) 2 -O-CH 3 ), R 8 - N(R 10 )(R 11 ) (e.g., (CH 2 ) 2 -NH(CH 3 ), (CH 2 ) 2 -NH 2 ), R 20 , or a substituted or unsubstituted 3-8 membered heterocyclic ring (e.g., pyrrolidine, piperidine); each represents a separate embodiment according to this invention.
  • R 8 -OH e.g., (CH 2 ) 2 -OH
  • -R 8 -O-R 10 e.g., (CH 2 ) 2 -O-CH 3
  • R 100 is H. In some embodiments, R 100 is C 1 -C 5 substituted or unsubstituted linear or branched alkyl. In some embodiments, R 100 is C 1 -C 5 unsubstituted linear or branched alkyl. In other embodiments, R 100 is CH 3 . In other embodiments, R 100 is CH 2 CH 3 . In other embodiments, R 100 is CH 2 CH 2 CH 3 . In some embodiments, R 100 is is isopropyl. In some embodiments, R 100 is butyl. In some embodiments, R 100 is isobutyl. In some embodiments, R 100 is t-butyl. In some embodiments, R 100 is pentyl.
  • R 100 is isopentyl. In some embodiments, R 100 is neopentyl. In some embodiments, R 100 is benzyl. In some embodiments, R 100 is C 1 -C 5 substituted linear or branched alkyl. In other embodiments, R 100 is CH 2 -CH 2 -O-CH 3 . In other embodiments, R 100 is CH 2 - CH 2 -OH. In other embodiments, R 100 is R 8 -OH. In other embodiments, R 100 is (CH 2 ) 2 -OH. In other embodiments, R 100 is -R 8 -O-R 10. In other embodiments, R 100 is (CH 2 ) 2 -O-CH 3 .
  • R 100 is R 8 -N(R 10 )(R 11 ). In other embodiments, R 100 is (CH 2 ) 2 -NH(CH 3 ). In other embodiments, R 100 is (CH 2 ) 2 -NH 2 . In other embodiments, R 100 is R 20 as defined hereinabove. In other embodiments, R 100 is a substituted or unsubstituted 3-8 membered heterocyclic ring. In other embodiments, R 100 is pyrrolidine. In other embodiments, R 100 is piperidine. In other embodiments, R 100 is C 1 -C 5 substituted or unsubstituted linear or branched haloalkyl.
  • R 100 is C 1 -C 5 linear or branched alkoxy. In other embodiments, R 100 is O-CH 3 . In other embodiments, R 100 is C(O)R. In other embodiments, R 100 is S(O) 2 R.
  • R 100 is further substituted with at least one substitution selected from: F, Cl, Br, I, C 1 -C 5 linear or branched alkyl, OH, alkoxy (e.g., OMe), amide (e.g., C(O)N(R) 2 , C(O)-pyrrolidine, C(O)-piperidine, N(R) 2 NH(R 10 ), N(R 10 )(R 11 ), (e.g., N(CH 3 ) 2 , NH 2 ), CF 3 , aryl, phenyl, heteroaryl, substituted or unsubstituted C 3 -C 8 cycloalkyl (e.g., cyclobutanol), substituted or unsubstituted 3-8 membered heterocyclic ring (e.g.
  • Ring W of formula I(j) and/or I(n) is a 3-10 membered single, fused, bridged or spiro, saturated, unsaturated or aromatic, carbocyclic or heterocyclic ring. In some embodiments, Ring W is a 3-8 membered single saturated heterocyclic ring.
  • Ring W is morpholine (e.g., 2 or 3-morpholine), tetrahydrofuran, tetrahydropyran, oxetane, pyrrolidine, piperazine, piperidine; each represents a separate embodiment according to this invention.
  • morpholine e.g., 2 or 3-morpholine
  • tetrahydrofuran tetrahydropyran
  • oxetane pyrrolidine
  • piperazine piperidine
  • Ring W is further substituted with R 200 to form a substituted heterocyclic ring, including but not limited to: oxetan-3-ol, pyrrolidin-2-ol, pyrrolidin-3-ol, 3-methoxypyrrolidine, 3- cyanopyrrolidine, 1-methylpyrrolidine, 3-(difluoromethyl)pyrrolidine, 3,3-difluoropyrrolidine, piperidin-3-ol, piperidin-4-ol, piperidine-4-carbonitrile, 4-fluoropiperidine, 2,2-dimethylpyrrolidine, pyrrolidin-3-one-O-methyloxime, 3,3-dimethylmorpholine or 1-methylpiperazine; each represents a separate embodiment according to this invention.
  • Ring W is a 3-8 membered single unsaturated heterocyclic ring.
  • Ring W is a pyrrolidin-2-one, pyrrolidin-3- one, pyrrolidinone, pyrrolidin-3-one-O-methyloxime, imidazole, pyrazole, isoxazolidine, piperidine-2- one, piperazine-2-one, oxadiazole, triazole, 2-oxopyrrolidine; each represents a separate embodiment according to this invention.
  • Ring W is a 3-10 membered spiro, saturated, heterocyclic ring.
  • Ring W is 4-azaspiro[2.4]heptane, 2-oxa-5- azaspiro[3.4]octane, 1,4-dioxa-6-azaspiro[4.4]nonane, 4,7-diazaspiro[2.5]octane; each represents a separate embodiment according to this invention.
  • Ring W is a 3-10 membered bridged, saturated, heterocyclic ring.
  • Ring W is bicyclo[1.1.1]pentane, 2,5- diazabicyclo[2.2.1]heptane; each represents a separate embodiment according to this invention.
  • Ring W is a 3-8 membered single saturated carbocyclic ring (i.e., cycloalkyl).
  • Ring W is cyclopropyl.
  • R 200 of formula I(j), I(k), I(l) and/or I(n) is H, R 20 , F, Cl, Br, I, OH, SH, alkoxy, NH 2 , N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), CF 3 , CN, NO 2 , C 1 -C 5 linear or branched, substituted or unsubstituted alkyl, methyl, ethyl, CH 2 -CH 2 -O-CH 2 -CH 2 -O-CH 3 , CH 2 -O-CH 2 -CH 2 -O-CH 3 , C 1 -C 5 linear or branched alkoxy, methoxy, C 1 -C 5 linear or branched haloalkyl, CHF 2 , CF 3 , CF 2 CH 3 , CH 2 CF 3, CF 2 CH 2 CH 3, CH 2 CH 2 CF 3, CF 2 CH(CH 2 CH(CH
  • R 200 is H. In some embodiments, R 200 is F. In some embodiments, R 200 is Cl. In some embodiments, R 200 is Br. In some embodiments, R 200 is I. In some embodiments, R 200 is OH. In some embodiments, R 200 is SH. In some embodiments, R 200 is alkoxy. In some embodiments, R 200 is NH 2 . In some embodiments, R 200 is N(R 10 )(R 11 ) . In some embodiments, R 200 is CF 3 . In some embodiments, R 200 is CN. In some embodiments, R 200 is NO 2 . In some embodiments, R 200 is C 1 -C 5 linear or branched, substituted or unsubstituted alkyl.
  • R 200 and the carbon atom to which it is connected are C(CH 3 ) 2 . In some embodiments, R 200 and the carbon atom to which it is connected are CF 2 .
  • Q 1 of formula I(k) is O. In some embodiments, Q 1 is NH. In some embodiments, Q 1 is CH 2 . In some embodiments, Q 1 is CH(R). In some embodiments, Q 1 is C(R) 2 .
  • t is 0. In some embodiments, t is 1. In some embodiments, t is 2. In some embodiments, t is 1 or 2. In some embodiments, t is between 1 and 3. In some embodiments, t is between 0 and 2. [00138] In various embodiments, this invention is directed to the compounds presented in Table 1, pharmaceutical compositions and/or method of use thereof, each represents a separate embodiment according to this invention: Table 1: P-597588-PC10 [00139] It is well understood that in structures presented in this invention wherein the carbon atom has less than 4 bonds, H atoms are present to complete the valence of the carbon.
  • this invention is directed to the compounds listed hereinabove, pharmaceutical compositions and/or method of use thereof, wherein the compound is pharmaceutically acceptable salt, stereoisomer, tautomer, hydrate, N-oxide, reverse amide analog, prodrug, isotopic variant (deuterated analog), PROTAC, pharmaceutical product or any combination thereof.
  • the compounds are c-MYC mRNA translation modulators.
  • the compounds are c-MYC mRNA translation inhibitors.
  • the compounds are c-MYC inhibitors.
  • the compounds are a c-MYC mRNA transcription regulators. In various embodiments, the compounds are any combination of c-MYC mRNA translation modulators, c- MYC mRNA transcription regulators and c-MYC inhibitors.
  • the term “alkyl” can be any straight- or branched-chain alkyl group containing up to about 30 carbons unless otherwise specified. In various embodiments, an alkyl includes C 1 -C 5 carbons. In some embodiments, an alkyl includes C 1 -C6 carbons. In some embodiments, an alkyl includes C 1 -C 5 carbons. In some embodiments, an alkyl includes C 1 -C8 carbons.
  • an alkyl includes C 1 -C10 carbons. In some embodiments, an alkyl is a C 1 -C12 carbons. In some embodiments, an alkyl is a C 1 -C20 carbons. In some embodiments, branched alkyl is an alkyl substituted by alkyl side chains of 1 to 5 carbons. In various embodiments, the alkyl group may be unsubstituted.
  • the alkyl group may be substituted by a halogen, haloalkyl, hydroxyl, alkoxy, carbonyl, amido, alkylamido, dialkylamido, cyano, nitro, CO 2 H, amino, alkylamino, dialkylamino, carboxyl, thio, thioalkyl, C 1 -C 5 linear or branched haloalkoxy, CF 3 , phenyl, halophenyl, (benzyloxy)phenyl, -CH 2 CN, NH 2 , NH-alkyl, N(alkyl) 2 , -OC(O)CF 3 , -OCH 2 Ph, -NHCO-alkyl, - C(O)Ph, C(O)O-alkyl, C(O)H, -C(O)NH 2 or any combination thereof.
  • the alkyl group can be a sole substituent, or it can be a component of a larger substituent, such as in an alkoxy, alkoxyalkyl, haloalkyl, arylalkyl, alkylamino, dialkylamino, alkylamido, alkylurea, etc.
  • Preferred alkyl groups are methyl, ethyl, and propyl, and thus halomethyl, dihalomethyl, trihalomethyl, haloethyl, dihaloethyl, trihaloethyl, halopropyl, dihalopropyl, trihalopropyl, methoxy, ethoxy, propoxy, arylmethyl, arylethyl, arylpropyl, methylamino, ethylamino, propylamino, dimethylamino, diethylamino, methylamido, acetamido, propylamido, halomethylamido, haloethylamido, halopropylamido, methyl-urea, ethyl-urea, propyl-urea, 2, 3, or 4-CH 2 -C 6 H 4 -Cl, C(OH)(CH 3 )(Ph), etc.
  • aryl refers to any aromatic ring that is directly bonded to another group and can be either substituted or unsubstituted.
  • the aryl group can be a sole substituent, or the aryl group can be a component of a larger substituent, such as in an arylalkyl, arylamino, arylamido, etc.
  • the term aryl according to this invention includes also heteroaryl.
  • Exemplary aryl groups include, without limitation, phenyl, tolyl, xylyl, furanyl, naphthyl, pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, triazinyl, thiazolyl, oxazolyl, isooxazolyl, pyrazolyl, imidazolyl, thiophene-yl, pyrrolyl, indolyl, phenylmethyl, phenylethyl, phenylamino, phenylamido, 3-methyl-4H-1,2,4-triazolyl, oxadiazolyl, 5-methyl-1,2,4-oxadiazolyl, isothiazolyl, thiadiazolyl, triazolyl, etc.
  • Substitutions include but are not limited to: F, Cl, Br, I, C 1 -C 5 linear or branched alkyl, C 1 -C 5 linear or branched haloalkyl, C 1 -C 5 linear or branched alkoxy, C 1 -C 5 linear or branched haloalkoxy, CF 3 , phenyl, halophenyl, CN, NO 2 , -CH 2 CN, NH 2 , NH-alkyl, N(alkyl) 2 , hydroxyl, -OC(O)CF 3 , -OCH 2 Ph, -NHCO-alkyl, COOH, - C(O)Ph, C(O)O-alkyl, C(O)H, -C(O)NH 2 or any combination thereof.
  • alkoxy refers to an ether group substituted by an alkyl group as defined above. Alkoxy refers both to linear and to branched alkoxy groups. Nonlimiting examples of alkoxy groups are methoxy, ethoxy, propoxy, iso-propoxy, tert-butoxy.
  • aminoalkyl refers to an amine group substituted by an alkyl group as defined above. Aminoalkyl refers to monoalkylamine, dialkylamine or trialkylamine. Nonlimiting examples of aminoalkyl groups are -N(Me) 2 , -NHMe, -NH3.
  • haloalkyl group refers, in some embodiments, to an alkyl group as defined above, which is substituted by one or more halogen atoms, e.g. by F, Cl, Br or I.
  • haloalkyl include but is not limited to fluoroalkyl, i.e., to an alkyl group bearing at least one fluorine atom.
  • Nonlimiting examples of haloalkyl groups are CF 3 , CF 2 CF 3 , CF 2 CH 3 , CH 2 CF 3 , CF 2 CH 2 CH 3 , CH 2 CH 2 CF 3 , CF 2 CH(CH 3 ) 2 and CF(CH 3 )-CH(CH 3 ) 2 .
  • a “halophenyl” group refers, in some embodiments, to a phenyl substitutent which is substituted by one or more halogen atoms, e.g. by F, Cl, Br or I. In one embodiment, the halophenyl is 4- chlorophenyl.
  • An “alkoxyalkyl” group refers, in some embodiments, to an alkyl group as defined above, which is substituted by alkoxy group as defined above, e.g. by methoxy, ethoxy, propoxy, i-propoxy, t- butoxy etc.
  • Nonlimiting examples of alkoxyalkyl groups are -CH 2 -O-CH 3 , -CH 2 -O-CH(CH 3 ) 2 , -CH 2 -O- C(CH 3 ) 3 , -CH 2 -CH 2 -O-CH 3 , -CH 2 -CH 2 -O-CH(CH 3 ) 2 , -CH 2 -CH 2 -O-C(CH 3 ) 3 .
  • a “cycloalkyl” or "carbocyclic" group refers, in various embodiments, to a ring structure comprising carbon atoms as ring atoms, which may be either saturated or unsaturated, substituted or unsubstituted, single or fused.
  • the cycloalkyl is a 3-10 membered ring. In some embodiments the cycloalkyl is a 3-12 membered ring. In some embodiments the cycloalkyl is a 6 membered ring. In some embodiments the cycloalkyl is a 5-7 membered ring. In some embodiments the cycloalkyl is a 3-8 membered ring.
  • the cycloalkyl group may be unsubstituted or substituted by a halogen, alkyl, haloalkyl, hydroxyl, alkoxy, carbonyl, amido, alkylamido, dialkylamido, cyano, nitro, CO 2 H, amino, alkylamino, dialkylamino, carboxyl, thio, thioalkyl, C 1 -C 5 linear or branched haloalkoxy, CF 3 , phenyl, halophenyl, (benzyloxy)phenyl, -CH 2 CN, NH 2 , NH-alkyl, N(alkyl) 2 , -OC(O)CF 3 , -OCH 2 Ph, - NHCO-alkyl, -C(O)Ph, C(O)O-alkyl, C(O)H, -C(O)NH 2 or any combination thereof.
  • the cycloalkyl ring may be fused to another saturated or unsaturated cycloalkyl or heterocyclic 3-8 membered ring. In some embodiments, the cycloalkyl ring is a saturated ring. In some embodiments, the cycloalkyl ring is an unsaturated ring.
  • Non limiting examples of a cycloalkyl group comprise cyclohexyl, cyclohexenyl, cyclopropyl, cyclopropenyl, cyclopentyl, cyclopentenyl, cyclopentadienyl, cyclobutyl, cyclobutenyl, cycloctyl, cycloctadienyl (COD), cycloctaene (COE) etc.
  • a “heterocycle” or “heterocyclic” group refers, in various embodiments, to a ring structure comprising in addition to carbon atoms, sulfur, oxygen, nitrogen or any combination thereof, as part of the ring.
  • heterocycle or heteroaromatic ring refers in various embodiments, to an aromatic ring structure comprising in addition to carbon atoms, sulfur, oxygen, nitrogen or any combination thereof, as part of the ring.
  • the heterocycle or heteroaromatic ring is a 3-10 membered ring.
  • the heterocycle or heteroaromatic ring is a 3-12 membered ring.
  • the heterocycle or heteroaromatic ring is a 6 membered ring.
  • the heterocycle or heteroaromatic ring is a 5-7 membered ring.
  • the heterocycle or heteroaromatic ring is a 3-8 membered ring.
  • the heterocycle group or heteroaromatic ring may be unsubstituted or substituted by a halogen, alkyl, haloalkyl, hydroxyl, alkoxy, carbonyl, amido, alkylamido, dialkylamido, cyano, nitro, CO 2 H, amino, alkylamino, dialkylamino, carboxyl, thio, thioalkyl, C 1 -C 5 linear or branched haloalkoxy, CF 3 , phenyl, halophenyl, (benzyloxy)phenyl, -CH 2 CN, NH 2 , NH-alkyl, N(alkyl) 2 , -OC(O)CF 3 , -OCH 2 Ph, - NHCO-alkyl, -C(O)Ph, C(O)O-alkyl, C(O)H, -C(O)NH 2 or any combination thereof.
  • the heterocycle ring or heteroaromatic ring may be fused to another saturated or unsaturated cycloalkyl or heterocyclic 3-8 membered ring.
  • the heterocyclic ring is a saturated ring.
  • the heterocyclic ring is an unsaturated ring.
  • Non limiting examples of a heterocyclic ring or heteroaromatic ring systems comprise pyridine, piperidine, morpholine, piperazine, thiophene, pyrrole, benzodioxole, benzofuran-2(3H)-one, benzo[d][1,3]dioxole, indole, oxazole, isoxazole, imidazole and 1-methylimidazole, furane, triazole, pyrimidine, pyrazine, oxacyclobutane (1 or 2- oxacyclobutane), naphthalene, tetrahydrothiophene 1,1-dioxide, thiazole, benzimidazole, piperidine, 1- methylpiperidine, isoquinoline, 1,3-dihydroisobenzofuran, benzofuran, 3-methyl-4H-1,2,4-triazole, oxadiazolyl, 5-methyl-1,2,
  • heterocyclic ring refers to substituted or unsubstituted, 3 to 8 membered, saturated, unsaturated or aromatic, single, fused or spiro rings, which comprise at least one heteroatom selected from: N, O or S.
  • the heterocyclic ring may be substituted, unsubstitutied, saturated, unsaturated, aromatic, single, fused or spiro ring; each represent a separate embodiment according to this invention.
  • the heterocyclic ring(s) may be 3-10; 3- 9; 3-8; 3-7; 3-6; 3-5; 4-6; 4-7; 4-8; 4-9; 5-6; 5-7; 5-8; 5-10 or 5-9 membered ring(s); each represents a separate embodiment according to this invention.
  • heterocyclic rings include, but ot limited to: pyran, tetrahydropyran, pyrrazole, imidazole, furan, tetrahydrofuran, dioxane, oxetane, azetidine, pyridine, pyridazine, pyrimidine, piperidine, piperazine, triazole, oxadiazole, tetrahydrofuran (THF), tetrahydrofurane, morpholine, thiomorpholine 1,1-dioxide, oxa-azaspirodecane, azaspiroheptane, 5- azaspiro[2.4]heptane, 2-azaspiro[3.3]heptane, oxa-azaspiroheptane, 2-oxa-6-azaspiro[3.3]heptane pyrrol, pyrrolidine, pyrrolidine-2-one, 2-oxo-pyrrolidine, pyr
  • the heterocyclic ring may be further substituted with at least one group selected from: F, Cl, Br, I, CF 3 , R 20 as defined hereinbelow, C 1 -C 5 linear or branched alkyl (e.g., methyl, ethyl, propyl), alkyleneamine (e.g., CH 2 -NH 2 ), C 1 -C 5 linear or branched haloalkyl (e.g., CH 2 CF 3 , CHF 2 ), OH, alkoxy (e.g., OCH 3 ), alkylene-OH (e.g., CH 2 -OH), amide, alkylene-amide (e.g., CH 2 -C(O)NH 2 ), C(O)- heterocyclic ring, amine (e.g., NH 2 ), alkylamine (e.g., NH(CH 3 )), dialkylamine (e.g., N(CH 3 ) 2 ), CF
  • “single or fused saturated, unsaturated or aromatic heterocyclic ring” or “saturated, unsaturated, aromatic, single, fused or spiro heterocyclic ring” can be any such ring(s), which comprise at least one heteroatom selected from: N, O or S, including but not limited to: pyridinyl, (2-, 3-, and 4-pyridinyl), quinolinyl, pyrimidinyl, pyridazinyl, pyrazinyl, triazinyl, tetrazinyl, thiazolyl, isothiazolyl, oxazolyl, isoxazolyl, imidazolyl, 1-methylimidazole, pyrazolyl, pyrrolyl, furanyl, thiophene-yl, quinolinyl, isoquinolinyl, 2,3-dihydroindenyl, indenyl, tetrahydronaph
  • the heterocyclic ring according to this invention includes: pyran, tetrahydropyran, pyrrazole, imidazole, furan, tetrahydrofuran, dioxane, oxetane, azetidine, pyridine, pyridazine, pyrimidine, piperidine, piperazine, triazole, oxadiazole, tetrahydrofuran (THF), tetrahydrofurane, morpholine, thiomorpholine 1,1-dioxide, oxa-azaspirodecane, azaspiroheptane, 5-azaspiro[2.4]heptane, 2-azaspiro[3.3]heptane, oxa-azaspiroheptane, pyrrol, pyrrolidine, pyrrolidine-2-one, 2-oxo-pyrrolidine, pyrrolidinone, quinuclidine, aze
  • the heterocyclic ring may be further substituted with at least one group selected from: F, Cl, Br, I, CF 3 , R 20 as defined hereinbelow, C 1 -C 5 linear or branched alkyl (e.g., methyl, ethyl, propyl), alkyleneamine (e.g., CH 2 -NH 2 ), C 1 -C 5 linear or branched haloalkyl (e.g., CH 2 CF 3 , CHF 2 ), OH, alkoxy (e.g., OCH 3 ), alkylene-OH (e.g., CH 2 -OH), amide, alkylene-amide (e.g., CH 2 -C(O)NH 2 ), C(O)-heterocyclic ring, amine (e.g., NH 2 ), alkylamine (e.g., NH(CH 3 )), dialkylamine (e.g., N(CH 3 ) 2 ),
  • this invention provides a compound of this invention or its isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, tautomer, hydrate, N-oxide, reverse amide analog, prodrug, isotopic variant (deuterated analog), PROTAC, polymorph, or crystal or combinations thereof.
  • this invention provides an isomer of the compound of this invention.
  • this invention provides a metabolite of the compound of this invention.
  • this invention provides a pharmaceutically acceptable salt of the compound of this invention.
  • this invention provides a pharmaceutical product of the compound of this invention.
  • this invention provides a tautomer of the compound of this invention.
  • this invention provides a hydrate of the compound of this invention. In some embodiments, this invention provides an N-oxide of the compound of this invention. In some embodiments, this invention provides a reverse amide analog of the compound of this invention. In some embodiments, “reverse amide analog” refers to acyclic amides or amides of acyclic amines. In some embodiments, this invention provides a prodrug of the compound of this invention. In some embodiments, this invention provides an isotopic variant (including but not limited to deuterated analog) of the compound of this invention. In some embodiments, this invention provides a PROTAC (Proteolysis targeting chimera) of the compound of this invention.
  • PROTAC Proteolysis targeting chimera
  • this invention provides a polymorph of the compound of this invention. In some embodiments, this invention provides a crystal of the compound of this invention. In some embodiments, this invention provides composition comprising a compound of this invention, as described herein, or, In some embodiments, a combination of an isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, tautomer, hydrate, N-oxide, reverse amide analog, prodrug, isotopic variant (deuterated analog), PROTAC, polymorph, or crystal of the compound of this invention.
  • the term “isomer” includes, but is not limited to, stereoisomers including optical isomers and analogs, structural isomers and analogs, conformational isomers and analogs, and the like.
  • the isomer is a stereoisomer.
  • the isomer is an optical isomer.
  • Certain compounds of the present invention may exist in particular geometric or stereoisomeric forms. The present invention contemplates all such compounds, including cis- and trans-isomers, R- and S-enantiomers, diastereomers, the racemic mixtures thereof, and other mixtures thereof, as falling within the scope of the invention.
  • asymmetric carbon atoms may be present in a substituent such as an alkyl group. All such isomers, as well as mixtures thereof, are included in this invention. [00156] In various embodiments, this invention encompasses the use of various stereoisomers of the compounds of the invention. It will be appreciated by those skilled in the art that the compounds of the present invention may contain at least one chiral center. Accordingly, the compounds used in the methods of the present invention may exist in, and be isolated in, optically-active or racemic forms.
  • the compounds according to this invention may further exist as stereoisomers which may be also optically- active isomers (e.g., enantiomers such as (R) or (S)), as enantiomerically enriched mixtures, racemic mixtures, or as single diastereomers, diastereomeric mixtures, or any other stereoisomers, including but not limited to: (R)(R), (R)(S), (S)(S), (S)(R), (R)(R)(R), (R)(R)(S), (R)(S)(R), (S)(R)(R), (R)(S)(R), (S)(R)(S), (S)(R)(S), (S)(S)(R)(R) or (S)(S)(S)(S) stereoisomers.
  • enantiomers such as (R) or (S)
  • the present invention encompasses any racemic, optically-active, polymorphic, or stereroisomeric form, or mixtures thereof, which form possesses properties useful in the treatment of the various conditions described herein.
  • optically active forms for example, by resolution of the racemic form by recrystallization techniques, by synthesis from optically-active starting materials, by chiral synthesis, or by chromatographic separation using a chiral stationary phase.
  • the compounds of the present invention can also be present in the form of a racemic mixture, containing substantially equivalent amounts of stereoisomers.
  • the compounds of the present invention can be prepared or otherwise isolated, using known procedures, to obtain a stereoisomer substantially free of its corresponding stereoisomer (i.e., substantially pure).
  • substantially pure it is intended that a stereoisomer is at least about 80% pure, more preferably at least about 95% pure, even more preferably at least about 98% pure, most preferably at least about 99% pure.
  • the compound according to the invention comprises a substantially pure stereoisomer.
  • the substantially pure stereoisomer is at least 70%; 75%; 80%; 85%; 90%; 93%; 95%; 97%; 98%; 99%; 99.5% pure; each represents a separate embodiment according to this invention.
  • the compound comprises a single stereoisomer in a purity of >80%; >85%; >90%; >91%; >92%; >93%; >94%; >95%; >96%; >97%; >98%; >99%; >99.5% enantiomeric excess (ee); each represents a separate embodiment according to this invention.
  • the compound comprises a single stereoisomer in a purity >80%; >85%; >90%; >91%; >92%; >93%; >94%; >95%; >96%; >97%; >98%; >99%; >99.5% enantiomeric ratio (er); each represents a separate embodiment according to this invention.
  • the compound comprises a single stereoisomer in a purity higher than 80%; 85%; 90%; 91%; 92%; 93%; 94%; 95%; 96%; 97%; 98%; 99%; 99.5%; each represents a separate embodiment according to this invention.
  • the compound is a substantially pure single enantiomer.
  • the compound comprises a mixture of enantiomers.
  • the compound is a racemate.
  • the compound has two chiral centers.
  • the compound comprises a mixture of stereoisomers.
  • the compound comprises a mixture of 2, 3, or 4 stereoisomers; each represents a separate embodiment according to this invention.
  • the compound is a single stereoisomer. In various embodiments, the compound is a substantially pure single stereoisomer. In various embodiments, the substantially pure stereoisomer has at least 80%, 85%, 90%, 95%, 97%, 98%, 99% purity; each represents a separate embodiment according to this invention. In various embodiments, the compound is the substantially pure RR stereoisomer. In various embodiments, the compound is the substantially pure SS stereoisomer. In various embodiments, the compound is the substantially pure RS stereoisomer. In various embodiments, the compound is the substantially pure SR stereoisomer.
  • Compounds of the present invention can also be in the form of a hydrate, which means that the compound further includes a stoichiometric or non-stoichiometric amount of water bound by non-covalent intermolecular forces.
  • a chemical functional group e.g., alkyl or aryl
  • substituted it is herein defined that one or more substitutions are possible.
  • the term “substituted” according to this invention refers to but is not limited to at least one group selected from: halogen, C 1 -C 5 linear or branched alkyl, OH, C 1 -C 5 linear or branched alkyl-OH (e.g., C(CH 3 ) 2 CH 2 -OH, CH 2 CH 2 -OH), alkoxy (e.g., OMe), amide (e.g., C(O)N(R) 2 , C(O)-pyrrolidine, C(O)- piperidine, N(R) 2 , NH(R 10 ), N(R 10 )(R 11 ), (e.g., N(CH 3 ) 2 , NH 2 ), CF 3 , aryl, phenyl, heteroaryl, substituted or unsubstituted C 3 -C 8 cycloalkyl (e.g., cyclobutanol), substituted or unsubstituted or unsubsti
  • pyran oxetane, piperidine, pyrazole, methyl-pyrrazole, triazole, imidazole), C 1 - C 5 linear or branched haloalkyl (e.g., CHF 2 , CH 2 CF 3 ), halophenyl, (benzyloxy)phenyl, CN and NO 2 ; each represents a separate embodiment according to this invention.
  • Compounds of the present invention may exist in the form of one or more of the possible tautomers and depending on the conditions it may be possible to separate some or all of the tautomers into individual and distinct entities.
  • the invention includes “pharmaceutically acceptable salts” of the compounds of this invention, which may be produced, by reaction of a compound of this invention with an acid or base. Certain compounds, particularly those possessing acidic or basic groups, can also be in the form of a salt, preferably a pharmaceutically acceptable salt.
  • pharmaceutically acceptable salt refers to those salts that retain the biological effectiveness and properties of the free bases or free acids, which are not biologically or otherwise undesirable.
  • the salts are formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid nitric acid phosphoric acid and the like, and organic acids such as acetic acid, propionic acid, glycolic acid, pyruvic acid, oxalic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid, N-acetylcysteine and the like.
  • inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid nitric acid phosphoric acid and the like
  • organic acids such as acetic acid, propionic acid, glycolic acid, pyruvic acid, oxalic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tart
  • Suitable pharmaceutically acceptable salts of amines of the compounds of this invention may be prepared from an inorganic acid or from an organic acid.
  • examples of inorganic salts of amines are bisulfates, borates, bromides, chlorides, hemisulfates, hydrobromates, hydrochlorates, 2-hydroxyethylsulfonates (hydroxyethanesulfonates), iodates, iodides, isethionates, nitrates, persulfates, phosphate, sulfates, sulfamates, sulfanilates, sulfonic acids (alkylsulfonates, arylsulfonates, halogen substituted alkylsulfonates, halogen substituted arylsulfonates), sulfonates and thiocyanates.
  • examples of organic salts of amines may be selected from aliphatic, cycloaliphatic, aromatic, araliphatic, heterocyclic, carboxylic and sulfonic classes of organic acids, examples of which are acetates, arginines, aspartates, ascorbates, adipates, anthranilates, alkane carboxylates, substituted alkane carboxylates, alginates, benzenesulfonates, benzoates, bisulfates, butyrates, bicarbonates, bitartrates, citrates, camphorates, camphorsulfonates, cyclohexylsulfamates, cyclopentanepropionates, calcium edetates, camsylates, carbonates, clavulanates, cinnamates, dicarboxylates, digluconates, dodecylsulfonates, dihydrochlorides, decanoates, enan
  • examples of inorganic salts of carboxylic acids or hydroxyls may be selected from ammonium, alkali metals to include lithium, sodium, potassium, cesium; alkaline earth metals to include calcium, magnesium, aluminium; zinc, barium, cholines, quaternary ammoniums.
  • examples of organic salts of carboxylic acids or hydroxyl may be selected from arginine, organic amines to include aliphatic organic amines, alicyclic organic amines, aromatic organic amines, benzathines, t-butylamines, benethamines (N-benzylphenethylamine), dicyclohexylamines, dimethylamines, diethanolamines, ethanolamines, ethylenediamines, hydrabamines, imidazoles, lysines, methylamines, meglumines, N-methyl-D-glucamines, N,N’- dibenzylethylenediamines, nicotinamides, organic amines, ornithines, pyridines, picolies, piperazines, procain, tris(hydroxymethyl)methylamines, triethylamines, triethanolamines, trimethylamines, tromethamines and ureas.
  • the salts may be formed by conventional means, such as by reacting the free base or free acid form of the product with one or more equivalents of the appropriate acid or base in a solvent or medium in which the salt is insoluble or in a solvent such as water, which is removed in vacuo or by freeze drying or by exchanging the ions of a existing salt for another ion or suitable ion-exchange resin.
  • Pharmaceutical composition [00171] Another aspect of the present invention relates to a pharmaceutical composition including a pharmaceutically acceptable carrier and a compound according to the aspects of the present invention.
  • the pharmaceutical composition can contain one or more of the above-identified compounds of the present invention.
  • the pharmaceutical composition of the present invention will include a compound of the present invention or its pharmaceutically acceptable salt, as well as a pharmaceutically acceptable carrier.
  • pharmaceutically acceptable carrier refers to any suitable adjuvants, carriers, excipients, or stabilizers, and can be in solid or liquid form such as, tablets, capsules, powders, solutions, suspensions, or emulsions.
  • the composition will contain from about 0.01 to 99 percent, preferably from about 20 to 75 percent of active compound(s), together with the adjuvants, carriers and/or excipients. While individual needs may vary, determination of optimal ranges of effective amounts of each component is within the skill of the art.
  • Typical dosages comprise about 0.01 to about 100 mg/kg body wt.
  • the preferred dosages comprise about 0.1 to about 100 mg/kg body wt.
  • the most preferred dosages comprise about 1 to about 100 mg/kg body wt.
  • Treatment regimen for the administration of the compounds of the present invention can also be determined readily by those with ordinary skill in art. That is, the frequency of administration and size of the dose can be established by routine optimization, preferably while minimizing any side effects.
  • the solid unit dosage forms can be of the conventional type.
  • the solid form can be a capsule and the like, such as an ordinary gelatin type containing the compounds of the present invention and a carrier, for example, lubricants and inert fillers such as, lactose, sucrose, or cornstarch.
  • these compounds are tabulated with conventional tablet bases such as lactose, sucrose, or cornstarch in combination with binders like acacia, cornstarch, or gelatin, disintegrating agents, such as cornstarch, potato starch, or alginic acid, and a lubricant, like stearic acid or magnesium stearate.
  • conventional tablet bases such as lactose, sucrose, or cornstarch in combination with binders like acacia, cornstarch, or gelatin
  • disintegrating agents such as cornstarch, potato starch, or alginic acid
  • a lubricant like stearic acid or magnesium stearate.
  • the tablets, capsules, and the like can also contain a binder such as gum tragacanth, acacia, corn starch, or gelatin; excipients such as dicalcium phosphate; a disintegrating agent such as corn starch, potato starch, alginic acid; a lubricant such as magnesium stearate; and a sweetening agent such as sucrose, lactose, or saccharin.
  • a binder such as gum tragacanth, acacia, corn starch, or gelatin
  • excipients such as dicalcium phosphate
  • a disintegrating agent such as corn starch, potato starch, alginic acid
  • a lubricant such as magnesium stearate
  • a sweetening agent such as sucrose, lactose, or saccharin.
  • a liquid carrier such as a fatty oil.
  • Various other materials may be present as coatings or to modify the physical form of the dosage unit. For instance, tablets can be coated with
  • a syrup can contain, in addition to active ingredient, sucrose as a sweetening agent, methyl and propylparabens as preservatives, a dye, and flavoring such as cherry or orange flavor.
  • these active compounds can be incorporated with excipients and used in the form of tablets, capsules, elixirs, suspensions, syrups, and the like.
  • Such compositions and preparations should contain at least 0.1% of active compound.
  • the percentage of the compound in these compositions can, of course, be varied and can conveniently be between about 2% to about 60% of the weight of the unit.
  • the amount of active compound in such therapeutically useful compositions is such that a suitable dosage will be obtained.
  • compositions according to the present invention are prepared so that an oral dosage unit contains between about 1 mg and 800 mg of active compound.
  • the active compounds of the present invention may be orally administered, for example, with an inert diluent, or with an assimilable edible carrier, or they can be enclosed in hard- or soft-shell capsules, or they can be compressed into tablets, or they can be incorporated directly with the food of the diet.
  • the pharmaceutical forms suitable for injectable use include sterile aqueous solutions or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersions. In all cases, the form should be sterile and should be fluid to the extent that easy syringability exists.
  • the carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (e.g., glycerol, propylene glycol, and liquid polyethylene glycol), suitable mixtures thereof, and vegetable oils.
  • the compounds or pharmaceutical compositions of the present invention may also be administered in injectable dosages by solution or suspension of these materials in a physiologically acceptable diluent with a pharmaceutical adjuvant, carrier or excipient.
  • Such adjuvants, carriers and/or excipients include, but are not limited to, sterile liquids, such as water and oils, with or without the addition of a surfactant and other pharmaceutically and physiologically acceptable components.
  • sterile liquids such as water and oils
  • Illustrative oils are those of petroleum, animal, vegetable, or synthetic origin, for example, peanut oil, soybean oil, or mineral oil.
  • water, saline, aqueous dextrose and related sugar solution, and glycols, such as propylene glycol or polyethylene glycol are preferred liquid carriers, particularly for injectable solutions.
  • These active compounds may also be administered parenterally. Solutions or suspensions of these active compounds can be prepared in water suitably mixed with a surfactant such as hydroxypropylcellulose.
  • Dispersions can also be prepared in glycerol, liquid polyethylene glycols, and mixtures thereof in oils.
  • oils are those of petroleum, animal, vegetable, or synthetic origin, for example, peanut oil, soybean oil, or mineral oil.
  • water, saline, aqueous dextrose and related sugar solution, and glycols such as, propylene glycol or polyethylene glycol are preferred liquid carriers, particularly for injectable solutions.
  • these preparations contain a preservative to prevent the growth of microorganisms.
  • the compounds of the present invention in solution or suspension may be packaged in a pressurized aerosol container together with suitable propellants, for example, hydrocarbon propellants like propane, butane, or isobutane with conventional adjuvants.
  • suitable propellants for example, hydrocarbon propellants like propane, butane, or isobutane with conventional adjuvants.
  • the materials of the present invention also may be administered in a non-pressurized form such as in a nebulizer or atomizer.
  • the compounds of this invention are administered in combination with an anti-cancer therapy. Examples of such therapies include but are not limited to: chemotherapy, immunotherapy, radiotherapy, biological therapy, surgical intervention, and combinations thereof.
  • the compound is administered in combination with an anti-cancer agent by administering the compounds as herein described, alone or in combination with other agents.
  • administering can be accomplished in any manner effective for delivering the compounds or the pharmaceutical compositions to the cancerous cells.
  • Exemplary modes of administration include, without limitation, administering the compounds or compositions orally, topically, transdermally, parenterally, subcutaneously, intravenously, intramuscularly, intraperitoneally, by intranasal instillation, by intracavitary or intravesical instillation, intraocularly, intraarterially, intralesionally, or by application to mucous membranes, such as, that of the nose, throat, and bronchial tubes.
  • Biological Activity [00184]
  • the invention provides compounds and compositions, including any embodiment described herein, for use in any of the methods of this invention.
  • compositions may further comprise additional active ingredients, whose activity is useful for the particular application for which the compound of this invention is being administered.
  • the invention relates to the treatment, inhibition, and reduction of cancer, employing the use of a compound according to this invention or a pharmaceutically acceptable salt thereof.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting cancer in a subject, comprising administering a compound according to this invention, to a subject suffering from cancer under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit cancer in said subject.
  • the compound is a c-MYC mRNA translation modulator.
  • the compound is a c-MYC mRNA translation inhibitor.
  • the compound is a c- MYC inhibitor.
  • the compound is a c-MYC mRNA transcription regulator.
  • the compound is any combination of a c-MYC mRNA translation modulator, a c- MYC mRNA transcription regulator and a c-MYC inhibitor.
  • the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • the cancer is early cancer. In some embodiments, the cancer is advanced cancer. In some embodiments, the cancer is invasive cancer. In some embodiments, the cancer is metastatic cancer. In some embodiments, the cancer is drug resistant cancer.
  • the cancer is selected from the following list: bladder cancer (urothelial carcinoma), myelodysplasia, breast cancer, cervix cancer, endometrium cancer, esophagus cancer, head and neck cancer (squamous cell carcinoma), kidney cancer (e.g., renal cell carcinoma, clear cell renal cell carcinoma), liver cancer (hepatocellular carcinoma), lung cancer (e.g., metastatic, non-small cell, NSCLC, squamous cell carcinoma, small cell (SCLC)), metastatic cacner (e.g., to brain), nasopharynx cancer, solid tumor cancer, stomach cancer, adrenocortical carcinoma, Glioblastoma multiforme, acute myeloid leukemia, chronic lymphocytic leukemia, lymphoma (e.g., Hodgkin's (classical), diffuse large B-cell, primary central nervous system), malignant melanoma, uveal melanoma, mening
  • bladder cancer urotheli
  • squamous cell biliary cancer
  • bladder cancer muscle invasive urothelial carcinoma
  • colorectal cancer metastatic colorectal cancer
  • fallopian tube cancer gastroesophageal junction cacner (e.g., adenocarcinoma), larynx cancer (e.g., squamous cell), merkel cell cancer, mouth cancer, ovary cancer (e.g., epithelial), pancreas cacner (e.g., adenocarcinoma, metastatic), penis cancer (e.g., squamous cell carcinoma), peritoneum cancer, prostate cancer (e.g., castration-resistant, metastatic), rectum cancer, skin cancer (e.g., basal cell carcinoma, squamous cell carcinoma), small intestine cancer (e.g., adenocarcinoma), testicular cancer, thymus cancer, anaplastic thyroid cancer, cholangiocarcinoma, chordoma,
  • the cancer is selected from a list including but not limited to: breast cancer, ovarian carcinoma, acute myeloid leukemia, chronic myelogenous leukemia, Hodgkin’s and Burkitt’s lymphoma, diffuse large Bcell lymphoma, prostate cancer, colon cancer, gastric cancer, primary central nervous system lymphoma, glioblastoma, medulloblastoma, melanoma, non-small cell lung carcinoma, germinal center-derived lymphomas, esophageal squamous cell carcinoma, osteosarcoma, bladder cancer, pancreatic cancer, lung adenocarcinoma, BRAF V600E thyroid cancer, choroid plexus carcinoma, colitis-associated cancer, epithelial ovarian cancer, colorectal cancer, pancreatic cancer and uterine cancer.
  • the cancer may be selected from solid tumors and non-solid tumors.
  • this invention is directed to a method for suppressing, reducing or inhibiting tumor growth in a subject, comprising administering a compound of this invention, to a subject under conditions effective to suppress, reduce or inhibit tumor growth in said subject.
  • the tumor may be a solid tumor or a non-solid tumor.
  • the solid tumor cancer is selected from a list including but not limited to: breast cancer, ovarian carcinoma, prostate cancer, colon cancer, gastric cancer, glioblastoma, medulloblastoma, melanoma, non-small cell lung carcinoma, esophageal squamous cell carcinoma, osteosarcoma, bladder cancer, pancreatic cancer, lung adenocarcinoma, BRAF V600E thyroid cancer, choroid plexus carcinoma, colitis-associated cancer, epithelial ovarian cancer, colorectal cancer, pancreatic cancer and uterine cancer.
  • the non-solid tumors include but not limited to: hematological malignancies including leukemia, lymphoma or myeloma and inherited cancers such as retinoblastoma and Wilm’s tumor.
  • the non-solid tumor cancer is selected from a list including but not limited to: acute myeloid leukemia, chronic myelogenous leukemia, Hodgkin’s and Burkitt’s lymphoma, diffuse large Bcell lymphoma, primary central nervous system lymphoma, glioblastoma, medulloblastoma, germinal center-derived lymphomas, myeloma, retinoblastoma and Wilm’s tumor.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting cancer comprising administering a compound of this invention to a subject suffering from cancer under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the cancer.
  • the cancer is early cancer.
  • the cancer is advanced cancer.
  • the cancer is invasive cancer.
  • the cancer is metastatic cancer.
  • the cancer is drug resistant cancer.
  • the compound is a c- MYC mRNA translation modulator.
  • the compound is a c-MYC mRNA translation inhibitor.
  • the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c-Myc protein in a cell. In some embodiments, the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention. [00196] In various embodiments, this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting breast cancer comprising administering a compound of this invention to a subject suffering from breast cancer under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the breast cancer. In some embodiments, the breast cancer is early breast cancer.
  • the breast cancer is advanced breast cancer. In some embodiments, the breast cancer is invasive breast cancer. In some embodiments, the breast cancer is metastatic breast cancer. In some embodiments, the breast cancer is drug resistant breast cancer. In some embodiments, the compound is a c-MYC mRNA translation modulator. In some embodiments, the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c-Myc protein in a cell. In some embodiments, the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting ovarian carcinoma comprising administering a compound of this invention to a subject suffering from ovarian carcinoma under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the ovarian carcinoma.
  • the ovarian carcinoma is early ovarian carcinoma.
  • the ovarian carcinoma is advanced ovarian carcinoma.
  • the ovarian carcinoma is invasive ovarian carcinoma.
  • the ovarian carcinoma is metastatic ovarian carcinoma.
  • the ovarian carcinoma is drug resistant ovarian carcinoma.
  • the compound is a c-MYC mRNA translation modulator. In some embodiments, the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c-Myc protein in a cell. In some embodiments, the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting acute myeloid leukemia comprising administering a compound of this invention to a subject suffering from acute myeloid leukemia under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the acute myeloid leukemia.
  • the acute myeloid leukemia is early acute myeloid leukemia.
  • the acute myeloid leukemia is advanced acute myeloid leukemia.
  • the acute myeloid leukemia is invasive acute myeloid leukemia.
  • the acute myeloid leukemia is metastatic acute myeloid leukemia.
  • the acute myeloid leukemia is drug resistant acute myeloid leukemia.
  • the compound is a c-MYC mRNA translation modulator. In some embodiments, the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c-Myc protein in a cell. In some embodiments, the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting chronic myelogenous leukemia comprising administering a compound of this invention to a subject suffering from chronic myelogenous leukemia under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the chronic myelogenous leukemia.
  • the chronic myelogenous leukemia is early chronic myelogenous leukemia.
  • the chronic myelogenous leukemia is advanced chronic myelogenous leukemia.
  • the chronic myelogenous leukemia is invasive chronic myelogenous leukemia.
  • the chronic myelogenous leukemia is metastatic chronic myelogenous leukemia. In some embodiments, the chronic myelogenous leukemia is drug resistant chronic myelogenous leukemia.
  • the compound is a c-MYC mRNA translation modulator. In some embodiments, the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c- Myc protein in a cell.
  • the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting Hodgkin’s and/or Burkitt’s lymphoma comprising administering a compound of this invention to a subject suffering from Hodgkin’s and/or Burkitt’s lymphoma under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the Hodgkin’s and/or Burkitt’s lymphoma.
  • the Hodgkin’s and/or Burkitt’s lymphoma is early Hodgkin’s and/or Burkitt’s lymphoma. In some embodiments, the Hodgkin’s and/or Burkitt’s lymphoma is advanced Hodgkin’s and/or Burkitt’s lymphoma. In some embodiments, the Hodgkin’s and/or Burkitt’s lymphoma is invasive Hodgkin’s and/or Burkitt’s lymphoma. In some embodiments, the Hodgkin’s and/or Burkitt’s lymphoma is metastatic Hodgkin’s and/or Burkitt’s lymphoma.
  • the Hodgkin’s and/or Burkitt’s lymphoma is drug resistant Hodgkin’s and/or Burkitt’s lymphoma.
  • the compound is a c-MYC mRNA translation modulator. In some embodiments, the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c-Myc protein in a cell. In some embodiments, the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting diffuse large Bcell lymphoma comprising administering a compound of this invention to a subject suffering from diffuse large Bcell lymphoma under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the diffuse large Bcell lymphoma.
  • the diffuse large Bcell lymphoma is early diffuse large Bcell lymphoma.
  • the diffuse large Bcell lymphoma is advanced diffuse large Bcell lymphoma.
  • the diffuse large Bcell lymphoma is invasive diffuse large Bcell lymphoma.
  • the diffuse large Bcell lymphoma is metastatic diffuse large Bcell lymphoma. In some embodiments, the diffuse large Bcell lymphoma is drug resistant diffuse large Bcell lymphoma. In some embodiments, the compound is a c-MYC mRNA translation modulator. In some embodiments, the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c-Myc protein in a cell. In some embodiments, the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting prostate cancer comprising administering a compound of this invention to a subject suffering from prostate cancer under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the prostate cancer.
  • the prostate cancer is early prostate cancer.
  • the prostate cancer is advanced prostate cancer.
  • the prostate cancer is invasive prostate cancer.
  • the prostate cancer is metastatic prostate cancer.
  • the prostate cancer is drug resistant prostate cancer.
  • the compound is a c-MYC mRNA translation modulator.
  • the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c- Myc protein in a cell. In some embodiments, the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting colon cancer comprising administering a compound of this invention to a subject suffering from colon cancer under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the colon cancer.
  • the colon cancer is early colon cancer.
  • the colon cancer is advanced colon cancer.
  • the colon cancer is invasive colon cancer.
  • the colon cancer is metastatic colon cancer.
  • the colon cancer is drug resistant colon cancer.
  • the compound is a c-MYC mRNA translation modulator.
  • the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c-Myc protein in a cell. In some embodiments, the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting gastric cancer comprising administering a compound of this invention to a subject suffering from gastric cancer under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the gastric cancer.
  • the gastric cancer is early gastric cancer.
  • the gastric cancer is advanced gastric cancer.
  • the gastric cancer is invasive gastric cancer.
  • the gastric cancer is metastatic gastric cancer.
  • the gastric cancer is drug resistant gastric cancer.
  • the compound is a c-MYC mRNA translation modulator.
  • the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c-Myc protein in a cell. In some embodiments, the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting lymphoma comprising administering a compound of this invention to a subject suffering from lymphoma under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the lymphoma.
  • the lymphoma is early lymphoma.
  • the lymphoma is advanced lymphoma.
  • the lymphoma is invasive lymphoma.
  • the lymphoma is metastatic lymphoma.
  • the lymphoma is drug resistant lymphoma.
  • the lymphoma is primary central nervous system lymphoma. In some embodiments, the lymphoma is germinal center-derived lymphoma. In some embodiments, the lymphoma is Hodgkin’s lymphoma. In some embodiments, the lymphoma is Burkitt’s lymphoma. In some embodiments, the lymphoma is diffuse large B-cell lymphoma. In some embodiments, the compound is a c-MYC mRNA translation modulator. In some embodiments, the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC.
  • the compound reduces the amount of c-Myc protein in a cell.
  • the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting glioblastoma comprising administering a compound of this invention to a subject suffering from glioblastoma under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the glioblastoma.
  • the glioblastoma is early glioblastoma.
  • the glioblastoma is advanced glioblastoma. In some embodiments, the glioblastoma is invasive glioblastoma. In some embodiments, the glioblastoma is metastatic glioblastoma. In some embodiments, the glioblastoma is drug resistant glioblastoma. In some embodiments, the compound is a c-MYC mRNA translation modulator. In some embodiments, the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC.
  • the compound reduces the amount of c-Myc protein in a cell.
  • the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting medulloblastoma comprising administering a compound of this invention to a subject suffering from medulloblastoma under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the medulloblastoma.
  • the medulloblastoma is early medulloblastoma.
  • the medulloblastoma is advanced medulloblastoma. In some embodiments, the medulloblastoma is invasive medulloblastoma. In some embodiments, the medulloblastoma is metastatic medulloblastoma. In some embodiments, the medulloblastoma is drug resistant medulloblastoma. In some embodiments, the compound is a c-MYC mRNA translation modulator. In some embodiments, the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC.
  • the compound reduces the amount of c-Myc protein in a cell.
  • the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting melanoma comprising administering a compound of this invention to a subject suffering from melanoma under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the melanoma.
  • the melanoma is early melanoma.
  • the melanoma is advanced melanoma.
  • the melanoma is invasive melanoma. In some embodiments, the melanoma is metastatic melanoma. In some embodiments, the melanoma is drug resistant melanoma. In some embodiments, the compound is a c-MYC mRNA translation modulator. In some embodiments, the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c- MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c-Myc protein in a cell.
  • the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting non-small cell lung carcinoma comprising administering a compound of this invention to a subject suffering from non-small cell lung carcinoma under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the non-small cell lung carcinoma.
  • the non-small cell lung carcinoma is early non-small cell lung carcinoma.
  • the non-small cell lung carcinoma is advanced non-small cell lung carcinoma.
  • the non-small cell lung carcinoma is invasive non-small cell lung carcinoma.
  • the non-small cell lung carcinoma is metastatic non-small cell lung carcinoma. In some embodiments, the non-small cell lung carcinoma is drug resistant non-small cell lung carcinoma. In some embodiments, the compound is a c-MYC mRNA translation modulator. In some embodiments, the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c- Myc protein in a cell. In some embodiments, the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting esophageal squamous cell carcinoma comprising administering a compound of this invention to a subject suffering from esophageal squamous cell carcinoma under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the esophageal squamous cell carcinoma.
  • the esophageal squamous cell carcinoma is early esophageal squamous cell carcinoma.
  • the esophageal squamous cell carcinoma is advanced esophageal squamous cell carcinoma.
  • the esophageal squamous cell carcinoma is invasive esophageal squamous cell carcinoma. In some embodiments, the esophageal squamous cell carcinoma is metastatic esophageal squamous cell carcinoma. In some embodiments, the esophageal squamous cell carcinoma is drug resistant esophageal squamous cell carcinoma.
  • the compound is a c-MYC mRNA translation modulator. In some embodiments, the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC.
  • the compound reduces the amount of c- Myc protein in a cell.
  • the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting osteosarcoma comprising administering a compound of this invention to a subject suffering from osteosarcoma under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the osteosarcoma.
  • the osteosarcoma is early osteosarcoma.
  • the osteosarcoma is advanced osteosarcoma.
  • the osteosarcoma is invasive osteosarcoma. In some embodiments, the osteosarcoma is metastatic osteosarcoma. In some embodiments, the osteosarcoma is drug resistant osteosarcoma. In some embodiments, the compound is a c-MYC mRNA translation modulator. In some embodiments, the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c-Myc protein in a cell.
  • the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting bladder cancer comprising administering a compound of this invention to a subject suffering from bladder cancer under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the bladder cancer.
  • the bladder cancer is early bladder cancer.
  • the bladder cancer is advanced bladder cancer.
  • the bladder cancer is invasive bladder cancer.
  • the bladder cancer is metastatic bladder cancer.
  • the bladder cancer is drug resistant bladder cancer.
  • the compound is a c-MYC mRNA translation modulator. In some embodiments, the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c-Myc protein in a cell. In some embodiments, the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting pancreatic cancer comprising administering a compound of this invention to a subject suffering from pancreatic cancer under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the pancreatic cancer.
  • the pancreatic cancer is early pancreatic cancer.
  • the pancreatic cancer is advanced pancreatic cancer.
  • the pancreatic cancer is invasive pancreatic cancer.
  • the pancreatic cancer is metastatic pancreatic cancer.
  • the pancreatic cancer is drug resistant pancreatic cancer.
  • the compound is a c-MYC mRNA translation modulator. In some embodiments, the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c-Myc protein in a cell. In some embodiments, the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting lung adenocarcinoma comprising administering a compound of this invention to a subject suffering from lung adenocarcinoma under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the lung adenocarcinoma.
  • the lung adenocarcinoma is early lung adenocarcinoma.
  • the lung adenocarcinoma is advanced lung adenocarcinoma.
  • the lung adenocarcinoma is invasive lung adenocarcinoma.
  • the lung adenocarcinoma is metastatic lung adenocarcinoma. In some embodiments, the lung adenocarcinoma is drug resistant lung adenocarcinoma. In some embodiments, the compound is a c- MYC mRNA translation modulator. In some embodiments, the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c-Myc protein in a cell.
  • the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting thyroid cancer comprising administering a compound of this invention to a subject suffering from thyroid cancerunder conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the thyroid cancer.
  • the thyroid cancer is early thyroid cancer.
  • the thyroid cancer is advanced thyroid cancer.
  • the thyroid cancer is invasive thyroid cancer.
  • the thyroid cancer is metastatic thyroid cancer.
  • the thyroid cancer is drug resistant thyroid cancer.
  • the thyroid cancer is BRAF V600E thyroid cancer.
  • the compound is a c-MYC mRNA translation modulator.
  • the compound is a c-MYC mRNA translation inhibitor.
  • the compound is a c-MYC mRNA transcription regulator.
  • the compound is selective to c-MYC.
  • the compound reduces the amount of c-Myc protein in a cell.
  • the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting choroid plexus carcinoma comprising administering a compound of this invention to a subject suffering from choroid plexus carcinoma under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the choroid plexus carcinoma.
  • the choroid plexus carcinoma is early choroid plexus carcinoma.
  • the choroid plexus carcinoma is advanced choroid plexus carcinoma.
  • the choroid plexus carcinoma is invasive choroid plexus carcinoma.
  • the choroid plexus carcinoma is metastatic choroid plexus carcinoma.
  • the choroid plexus carcinoma is drug resistant choroid plexus carcinoma.
  • the compound is a c-MYC mRNA translation modulator. In some embodiments, the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c-Myc protein in a cell. In some embodiments, the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • the compound is a c-MYC mRNA translation modulator. In some embodiments, the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c-Myc protein in a cell. In some embodiments, the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting ovarian cancer comprising administering a compound of this invention to a subject suffering from ovarian cancer under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the ovarian cancer.
  • the ovarian cancer is early ovarian cancer.
  • the ovarian cancer is advanced ovarian cancer .
  • the ovarian cancer is invasive ovarian cancer.
  • the ovarian cancer is metastatic ovarian cancer.
  • the ovarian cancer is drug resistant ovarian cancer.
  • the ovarian cancer is epithelial ovarian cancer.
  • the compound is a c-MYC mRNA translation modulator.
  • the compound is a c-MYC mRNA translation inhibitor.
  • the compound is a c-MYC mRNA transcription regulator.
  • the compound is selective to c-MYC.
  • the compound reduces the amount of c-Myc protein in a cell.
  • the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting colorectal cancer comprising administering a compound of this invention to a subject suffering from colorectal cancer under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the colorectal cancer.
  • the colorectal cancer is early colorectal cancer.
  • the colorectal cancer is advanced colorectal cancer.
  • the colorectal cancer is invasive colorectal cancer.
  • the colorectal cancer is metastatic colorectal cancer.
  • the colorectal cancer is drug resistant colorectal cancer.
  • the compound is a c-MYC mRNA translation modulator. In some embodiments, the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c-Myc protein in a cell. In some embodiments, the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention is directed to a method of treating, suppressing, reducing the severity, reducing the risk of developing or inhibiting uterine cancer comprising administering a compound of this invention to a subject suffering from uterine cancer under conditions effective to treat, suppress, reduce the severity, reduce the risk of developing, or inhibit the uterine cancer.
  • the uterine cancer is early uterine cancer.
  • the uterine cancer is advanced uterine cancer.
  • the uterine cancer is invasive uterine cancer.
  • the uterine cancer is metastatic uterine cancer.
  • the uterine cancer is drug resistant uterine cancer.
  • the compound is a c-MYC mRNA translation modulator. In some embodiments, the compound is a c-MYC mRNA translation inhibitor. In some embodiments, the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c-Myc protein in a cell. In some embodiments, the compound is any one of the compounds listed in Table 1; each compound represents a separate embodiment according to this invention.
  • this invention provides methods for increasing the survival of a subject suffering from metastatic cancer comprising the step of administering to said subject a compound of this invention and/or an isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, tautomer, hydrate, N-oxide, reverse amide analog, prodrug, isotopic variant (e.g., deuterated analog), PROTAC, polymorph, or crystal of said compound, or any combination thereof.
  • the compound is a c-MYC mRNA translation modulator.
  • the compound is a c- MYC mRNA translation inhibitor.
  • the compound is a c-MYC mRNA transcription regulator.
  • the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c-Myc protein in a cell.
  • the cancer is breast cancer, ovarian carcinoma, acute myeloid leukemia, chronic myelogenous leukemia, Hodgkin’s and Burkitt’s lymphoma, diffuse large Bcell lymphoma, prostate cancer, colon cancer, gastric cancer, primary central nervous system lymphoma, glioblastoma, medulloblastoma, melanoma, non- small cell lung carcinoma, germinal center-derived lymphomas, esophageal squamous cell carcinoma, osteosarcoma, bladder cancer, pancreatic cancer, lung adenocarcinoma, thyroid cancer, choroid plexus carcinoma, colitis-associated cancer, colorectal cancer, or uterine cancer; each represents a separate embodiment according to this invention.
  • this invention provides methods for treating, suppressing, reducing the severity, reducing the risk, or inhibiting advanced cancer comprising the step of administering to said subject a compound of this invention and/or an isomer, metabolite, pharmaceutically acceptable salt, pharmaceutical product, tautomer, hydrate, N-oxide, reverse amide analog, prodrug, isotopic variant (e.g., deuterated analog), PROTAC, polymorph, or crystal of said compound, or any combination thereof.
  • the compound is a c-MYC mRNA translation modulator.
  • the compound is a c-MYC mRNA translation inhibitor.
  • the compound is a c-MYC mRNA transcription regulator. In some embodiments, the compound is selective to c-MYC. In some embodiments, the compound reduces the amount of c-Myc protein in a cell.
  • the cancer is breast cancer, ovarian carcinoma, acute myeloid leukemia, chronic myelogenous leukemia, Hodgkin’s and Burkitt’s lymphoma, diffuse large Bcell lymphoma, prostate cancer, colon cancer, gastric cancer, primary central nervous system lymphoma, glioblastoma, medulloblastoma, melanoma, non-small cell lung carcinoma, germinal center-derived lymphomas, esophageal squamous cell carcinoma, osteosarcoma, bladder cancer, pancreatic cancer, lung adenocarcinoma, thyroid cancer, choroid plexus carcinoma, colitis-associated cancer, colorectal cancer, or uterine cancer; each represents a separate embodiment according to
  • the compounds of the present invention are useful in the treatment, reducing the severity, reducing the risk of developing, or inhibition of early cancer, metastatic cancer, advanced cancer, drug resistant cancer, and various forms of cancer.
  • the cancer is breast cancer, ovarian carcinoma, acute myeloid leukemia, chronic myelogenous leukemia, Hodgkin’s and Burkitt’s lymphoma, diffuse large Bcell lymphoma, prostate cancer, colon cancer, gastric cancer, primary central nervous system lymphoma, glioblastoma, medulloblastoma, melanoma, non-small cell lung carcinoma, germinal center- derived lymphomas, esophageal squamous cell carcinoma, osteosarcoma, bladder cancer, pancreatic cancer, lung adenocarcinoma, thyroid cancer, choroid plexus carcinoma, colitis-associated cancer, colorectal cancer, or uterine cancer; each represents a separate embodiment accordin g to this invention.
  • Preferred compounds of the present invention are selectively disruptive to cancer cells, causing ablation of cancer cells but preferably not normal cells. Significantly, harm to normal cells is minimized because the cancer cells are susceptible to disruption at much lower concentrations of the compounds of the present invention.
  • the cancer is invasive. In some embodiments the cancer is metastatic cancer. In some embodiments the cancer is advanced cancer. In some embodiments the cancer is drug resistant cancer. [00225] In various embodiments “metastatic cancer” refers to a cancer that spread (metastasized) from its original site to another area of the body. Virtually all cancers have the potential to spread. Whether metastases develop depends on the complex interaction of many tumor cell factors, including the type of cancer, the degree of maturity (differentiation) of the tumor cells, the location and how long the cancer has been present, as well as other incompletely understood factors. Metastases spread in three ways - by local extension from the tumor to the surrounding tissues, through the bloodstream to distant sites or through the lymphatic system to neighboring or distant lymph nodes.
  • drug-resistant cancer refers to cancer cells that acquire resistance to chemotherapy. Cancer cells can acquire resistance to chemotherapy by a range of mechanisms, including the mutation or overexpression of the drug target, inactivation of the drug, or elimination of the drug from the cell. Tumors that recur after an initial response to chemotherapy may be resistant to multiple drugs (they are multidrug resistant). In the conventional view of drug resistance, one or several cells in the tumor population acquire genetic changes that confer drug resistance.
  • the reasons for drug resistance are: a) some of the cells that are not killed by the chemotherapy mutate (change) and become resistant to the drug. Once they multiply, there may be more resistant cells than cells that are sensitive to the chemotherapy; b) Gene amplification. A cancer cell may produce hundreds of copies of a particular gene.
  • This gene triggers an overproduction of protein that renders the anticancer drug ineffective; c) cancer cells may pump the drug out of the cell as fast as it is going in using a molecule called p-glycoprotein; d) cancer cells may stop taking in the drugs because the protein that transports the drug across the cell wall stops working; e) the cancer cells may learn how to repair the DNA breaks caused by some anti-cancer drugs; f) cancer cells may develop a mechanism that inactivates the drug.
  • P-gp P-glycoprotein
  • This protein is a clinically important transporter protein belonging to the ATP-binding cassette family of cell membrane transporters.
  • resistant cancer refers to drug-resistant cancer as described herein above. In some embodiments “resistant cancer” refers to cancer cells that acquire resistance to any treatment such as chemotherapy, radiotherapy or biological therapy.
  • this invention is directed to treating, suppressing, reducing the severity, reducing the risk of developing, or inhibiting cancer in a subject, wherein the subject has been previously treated with chemotherapy, radiotherapy or biological therapy.
  • “Chemotherapy” refers to chemical treatment for cancer such as drugs that kill cancer cells directly. Such drugs are referred as "anti-cancer” drugs or "antineoplastics.” Today's therapy uses more than 100 drugs to treat cancer. Chemotherapy is used to control tumor growth when cure is not possible; to shrink tumors before surgery or radiation therapy; to relieve symptoms (such as pain); and to destroy microscopic cancer cells that may be present after the known tumor is removed by surgery (called adjuvant therapy).
  • Radiotherapy also referred herein as “Radiation therapy” refers to high energy x-rays and similar rays (such as electrons) to treat disease. Many people with cancer will have radiotherapy as part of their treatment. This can be given either as external radiotherapy from outside the body using x-rays or from within the body as internal radiotherapy. Radiotherapy works by destroying the cancer cells in the treated area. Although normal cells can also be damaged by the radiotherapy, they can usually repair themselves. Radiotherapy treatment can cure some cancers and can also reduce the chance of a cancer coming back after surgery. It may be used to reduce cancer symptoms.
  • Bio therapy refers to substances that occur naturally in the body to destroy cancer cells. There are several types of treatment including: monoclonal antibodies, cancer growth inhibitors, vaccines and gene therapy. Biological therapy is also known as immunotherapy.
  • the pharmaceutical composition can also contain, or can be administered in conjunction with, other therapeutic agents or treatment regimen presently known or hereafter developed for the treatment of various types of cancer. Examples of other therapeutic agents or treatment regimen include, without limitation, radiation therapy, immunotherapy, chemotherapy, surgical intervention, and combinations thereof.
  • the compound according to this invention is administered in combination with an anti-cancer therapy.
  • anti-cancer therapy examples include but are not limited to: chemotherapy, immunotherapy, radiotherapy, biological therapy, surgical intervention, and combinations thereof.
  • the compound is administered in combination with an anti-cancer agent by administering the compounds as herein described, alone or in combination with other agents.
  • the composition for cancer treatment of the present invention can be used together with existing chemotherapy drugs or be made as a mixture with them.
  • Such a chemotherapy drug includes, for example, alkylating agents, nitrosourea agents, antimetabolites, antitumor antibiotics, alkaloids derived from plant, topoisomerase inhibitors, hormone therapy medicines, hormone antagonists, aromatase inhibitors, P-glycoprotein inhibitors, platinum complex derivatives, other immunotherapeutic drugs, and other anticancer agents. Further, they can be used together with hypoleukocytosis (neutrophil) medicines that are cancer treatment adjuvant, thrombopenia medicines, antiemetic drugs, and cancer pain medicines for patient's QOL recovery or be made as a mixture with them.
  • hypoleukocytosis neurotrophil
  • this invention provides a method of modulating c-MYC mRNA translation in a cell, comprising contacting a compound represented by the structure of formula I, II and/or I(a)-I(o) and/or by the structures listed in Table 1, as defined herein above, with a cell, thereby modulating c-MYC mRNA translation in said cell.
  • the method is carried out by regulating c-MYC mRNA splicing.
  • the method is carried out by inclusion or exclusion of untranslated region or alternative usage of exons.
  • the method is carried out by regulation of c-MYC mRNA modifications.
  • the method is carried out by regulation of the interaction of RNA binding protein with c-MYC mRNA thereby changing mRNA localization. In some embodiments, the method is carried out by regulating c-MYC mRNA localization in the cytoplasm. In some embodiments, the method is carried out by regulating ribosomes or ribosome accessory factor to c-MYC mRNA. In some embodiments, the method is carried out by reducing the amount of c-MYC protein in the cell.
  • This invention further provides a method of regulating c-MYC mRNA transcription in a cell, comprising contacting a compound represented by the structure of formula I, II and/or I(a)-I(o) and/or by the structures listed in Table 1, as defined herein above, with a cell, thereby regulating c-MYC mRNA transcription in said cell.
  • the method is carried out by regulating c-MYC mRNA splicing.
  • the method is carried out by inclusion or exclusion of untranslated region or alternative usage of exons.
  • the method is carried out by regulation of c-MYC mRNA modifications.
  • the method is carried out by regulation of the interaction of RNA binding protein with c-MYC mRNA thereby changing mRNA localization. In some embodiments, the method is carried out by regulating c-MYC mRNA localization in the cytoplasm. In some embodiments, the method is carried out by regulating ribosomes or ribosome accessory factor to c-MYC mRNA. In some embodiments, the method is carried out by reducing the amount of c-MYC protein in the cell. [00238] In various embodiments, this invention is directed to a method of destroying a cancerous cell comprising providing a compound of this invention and contacting the cancerous cell with the compound under conditions effective to destroy the contacted cancerous cell.
  • the cells to be destroyed can be located either in vivo or ex vivo (i.e., in culture).
  • a still further aspect of the present invention relates to a method of treating or preventing a cancerous condition that includes providing a compound of the present invention and then administering an effective amount of the compound to a patient in a manner effective to treat or prevent a cancerous condition.
  • the patient to be treated is characterized by the presence of a precancerous condition, and the administering of the compound is effective to prevent development of the precancerous condition into the cancerous condition. This can occur by destroying the precancerous cell prior to or concurrent with its further development into a cancerous state.
  • the patient to be treated is characterized by the presence of a cancerous condition, and the administering of the compound is effective either to cause regression of the cancerous condition or to inhibit growth of the cancerous condition, i.e., stopping its growth altogether or reducing its rate of growth.
  • This preferably occurs by destroying cancer cells, regardless of their location in the patient body. That is, whether the cancer cells are located at a primary tumor site or whether the cancer cells have metastasized and created secondary tumors within the patient body.
  • subject or patient refers to any mammalian patient, including without limitation, humans and other primates, dogs, cats, horses, cows, sheep, pigs, rats, mice, and other rodents.
  • the subject is male. In some embodiments, the subject is female. In some embodiments, while the methods as described herein may be useful for treating either males or females. [00243]
  • administering the compounds of the present invention they can be administered systemically or, alternatively, they can be administered directly to a specific site where cancer cells or precancerous cells are present. Thus, administering can be accomplished in any manner effective for delivering the compounds or the pharmaceutical compositions to the cancer cells or precancerous cells.
  • Exemplary modes of administration include, without limitation, administering the compounds or compositions orally, topically, transdermally, parenterally, subcutaneously, intravenously, intramuscularly, intraperitoneally, by intranasal instillation, by intracavitary or intravesical instillation, intraocularly, intraarterially, intralesionally, or by application to mucous membranes, such as, that of the nose, throat, and bronchial tubes.
  • EXAMPLE 1 General Synthetic Details for Compounds of the Invention (Schemes 1-22) General Methods [00245] All reagents were commercial grade and were used as received without further purification, unless otherwise specified. Reagent grade solvents were used in all cases, unless otherwise specified. Thin layer chromatography was carried out using pre-coated silica gel F-254 plates (thickness 0.25 mm). 1 H- NMR and 19 F-NMR spectra were recorded on a Bruker Bruker Avance 400MHz or Avance III 400MHz spectrometer. The chemical shifts are expressed in ppm using the residual solvent as internal standard.
  • Splitting patterns are designated as s (singlet), d (doublet), dd (doublet of doublets), t (triplet), dt (doublet of triplets), q (quartet), m (multiplet) and br s (broad singlet).
  • Cross-coupling partners to introduce R 2 include various boronic acid / esters (Suzuki-Miyaura coupling) or various organostannane reagents (Stille coupling) to furnish the final compounds with various right-hand sides (RHS), Structure I. Synthesis of benzo[d]imidazo[2,1-b]thiazole compounds, Structure II Scheme 2. Second generation synthesis of benzo[d]imidazo[2,1-b]thiazole compounds, Structure II.
  • the first step of the synthesis involves bromination of the ⁇ -carbonyl position of various substituted aryl methyl ketones 6, using pyridinium tribromide in the presence of HBr in acetic acid affording substituted phenacyl bromide intermediates 7.
  • These intermediates 7 facilitate ready diversification of the right-hand side (RHS) of the final compounds, Structure II.
  • Intermediate 7 undergoes a alkylation reaction followed by intramolecular cyclization with ethyl 2- aminobenzothiazole-6-carboxylate 1 at elevated temperature to from ester benzo[d]imidazo[2,1- b]thiazole intermediate 8. Hydrolysis of ester intermediate 8 with sodium hydroxide in water/THF mixture affords acid intermediate 9.
  • the final step involves an amide coupling of various primary ⁇ secondary amines with acid intermediate 9, using HATU as a coupling reagent delivering the final compounds with various left-hand side (LHS) amides, Structure II.
  • HATU left-hand side
  • the first step involves a “one-pot” alkylation and intramolecular cyclization reaction between substituted phenacyl bromide intermediates 7 (as in Scheme 2) and 2-amino-6- bromobenzothiazole 10 at elevated temperature affording 7-bromo-2-aryl-lbenzo[d]imidazo[2,1- b]thiazole intermediates 11.
  • the bromo heterocyclic intermediate 11 is employed as the key starting material for the final palladium-catalyzed aminocarbonylation reaction at elevated temperature.
  • Various primary ⁇ secondary amines are used in this final palladium-catalyzed aminocarbonylation reaction to provide a variety of left-hand side (LHS) amides, Structure II.
  • the thiol moiety is introduced by reaction of the 2-chlorobenzimidazole intermediate 3 with thiourea at elevated temperature to form intermediate 4.
  • the third step involves “one pot” acetylation and intramolecular cyclization, using acetic anhydride and sulfuric acid to generate the tricyclic benzo[4,5]imidazo[2,1-b]thiazole ester intermediate 5.
  • Hydrolysis of the methyl ester intermediate 5 using sodium hydroxide in a water/THF mixture gave carboxylic acid intermediate 6.
  • Amide coupling reaction between carboxylic acid intermediate 6 and methylamine hydrochloride, using HATU as a coupling reagent affords the important methylamide intermediate 7.
  • the bromo heteroaryl moiety of intermediate 7 is used in the final palladium-catalyzed aminocarbonylation reaction at elevated temperature with a variety of primary/secondary amines to deliver the final left-hand side (LHS) amides, Structure IV.
  • the first step of the synthesis involves electrophilic amination reaction of ethyl 2- aminobenzothiazole-6-carboxylate 1 with O-(2,4,6-trimethylbenzenesulfonyl)hydroxylamine (MSH) 2 in DCM affording the salt intermediate 3.
  • the salt intermediate 3 undergoes an amide coupling reaction with various terephthalic acids 4, using HATU to provide the mono acylated intermediate 5.
  • Step four of the synthesis involves alkylation of the amino moiety of intermediate 5 with 4-carboxylic acid substituted phenacyl bromides 6 followed by intramolecular cyclization in refluxing ethanol to form the imidazothiazolo[4,5-b]pyridine benzoic acid intermediate 7.
  • Amide coupling reaction of the benzoic acid intermediate 7 with methylamine hydrochloride using HATU as the coupling reagent affords the methylamide intermediate 8.
  • the 7-bromo heteroaryl moiety of intermediate 8 undergoes a palladium-catalyzed aminocarbonylation reaction at elevated temperature, using various primary/secondary amines to furnish the desired 4- (methylcarbamoyl)phenyl)imidazo[2',1':2,3]thiazolo[4,5-b]pyridine-7-carboxamide compounds, Structure VI. Synthesis of 4-(methylcarbamoyl)phenyl)imidazo[2',1':2,3]thiazolo[5,4-b]pyridine-7-carboxamide compounds, Structure VII Scheme 8.
  • the first step of the synthesis involves reaction of potassium thiocyanate and substituted 2,6- dichloro-3-pyridinamine 1 in refluxing ethanol, in the presence of concentrated aqueous hydrochloric acid affording the 5-chlorothiazolo[5,4-b]pyridin-2-amine intermediate 2.
  • the second step involves alkylation of the amino moiety of intermediate 2 with 4-carboxylic acid substituted phenacyl bromides 3 followed by intramolecular cyclization in refluxing dioxane to form the imidazothiazolo[5,4- b]pyridine benzoic acid intermediate 4.
  • Amide coupling reaction of the benzoic acid intermediate 4 with methylamine hydrochloride, using HATU as the coupling reagent affords the methylamide intermediate 5.
  • the 7-chloro heteroaryl moiety of intermediate 5 undergoes a palladium-catalyzed aminocarbonylation reaction at elevated temperature, using various primary/secondary amines to furnish the desired 4-(methylcarbamoyl)phenyl)imidazo[2',1':2,3]thiazolo[5,4-b]pyridine-7-carboxamide compounds, Structure VII.
  • the first step of the synthesis involves reaction of potassium thiocyanate with a 6-substituted 2,4-dichloropyrimidin-5-amine 1 in acetic acid at elevated temperature affording the 5- chlorothiazolo[5,4-d]pyrimidin-2-amine intermediate 2.
  • the second step involves alkylation of the amino moiety of intermediate 2 with 4-carboxylic acid substituted phenacyl bromides 3 followed by intramolecular cyclization in refluxing dioxane to generate the imidazo[2',1':2,3]thiazolo[5,4- d]pyrimidin-7-yl)benzoic acid intermediate 4.
  • Amide coupling reaction of the benzoic acid intermediate 4 with methylamine hydrochloride, using HATU as the coupling reagent affords the methylamide intermediate 5.
  • the 2-chloroimidazolo moiety of intermediate 5 undergoes a palladium- catalyzed aminocarbonylation reaction at elevated temperature, using various primary/secondary amines to deliver the desired 4-(methylcarbamoyl)phenyl)imidazo[2',1':2,3]thiazolo[5,4-d]pyrimidine-2- carboxamide compounds, Structure VIII.
  • Synthesis of 4-(methylcarbamoyl)phenyl)imidazo[2',1':2,3]thiazolo[4,5-c]pyridine-7-carboxamide compounds Structure IX Scheme 10.
  • the first step of the synthesis involves reaction of potassium thiocyanate with a substituted 4,6-dichloropyridin-3-amine 1 in refluxing ethanol, in the presence of concentrated aqueous hydrochloric acid affording the 6-chlorothiazolo[4,5-c]pyridin-2-amine intermediate 2.
  • the second step involves alkylation of the amino moiety of intermediate 2 with 4-carboxylic acid substituted phenacyl bromides 3 followed by intramolecular cyclization in refluxing dioxane to generate the imidazo[2',1':2,3]thiazolo[4,5-c]pyridin-2-yl)benzoic acid intermediate 4.
  • Amide coupling reaction of the benzoic acid intermediate 4 with methylamine hydrochloride, using HATU as the coupling reagent affords the methylamide intermediate 5.
  • the 7-chloro heteroaryl moiety of intermediate 5 undergoes a palladium-catalyzed aminocarbonylation reaction at elevated temperature, using various primary/secondary amines to deliver the desired 4- (methylcarbamoyl)phenyl)imidazo[2',1':2,3]thiazolo[4,5-c]pyridine-7-carboxamide compounds, Structure IX.
  • the first step of the synthesis involved primary amide formation from substituted aryl carboxylic acids 1. This was achieved using ammonium chloride and coupling reagents such as CDI or HATU to afford primary amide intermediates 2 and nitrile intermediates 3. Reduction of mixtures of 2 or 3 using borane in THF at elevated temperatures and subsequent protecting group strategy afforded intermediates 4. Palladium-mediated, Miyaura borylation of aryl bromide intermediates 4 gave the desired aryl boronic ester intermediates 6.
  • the final step of the synthetic sequence involved acid mediated N-Boc deprotection of intermediates 7.
  • the first step of the synthesis involved primary amide formation from substituted aryl carboxylic acids 6 (as in Scheme 5). This was achieved using ammonium chloride and coupling reagents such as CDI or HATU to afford primary amide intermediates 9. Reduction of intermediates 9 using borane in THF at elevated temperatures and subsequent protecting group strategy afforded intermediates 10. Intermediates 10 were subjected to palladium-catalyzed aminocarbonylation with the desired amine (as in Scheme 3) at elevated temperature to provide intermediates 7. Acid mediated deprotection of intermediates 7 gave final compounds, Structure X.
  • Intermediates 20 are deprotected under acidic conditions to generate intermediates 21.
  • Intermediates 16 undergo the same synthetic procedure as outlined in Scheme 11 to generate final compounds, Structure XIII.
  • intermediates 24 were separated by chiral HPLC/SFC to generate two enantiomers. The resulting intermediates were deprotected using acidic conditions, to generate the enantiomers of Structure XIII.
  • Synthesis of benzo[d]imidazo[2,1-b]thiazole compounds Structure IXV Scheme 16.
  • the first step of the synthesis involved amide formation from substituted aryl carboxylic acids 1.
  • Intermediates 40 were then subsequently treated with Boc2O under basic conditions to give intermediates 41.
  • Hydrolysis of ester intermediates 41 with lithium hydroxide in a mixture of water/THF/MeOH afforded carboxylic acid intermediates 42.
  • Intermediates 42 were subjected to HATU mediated amide coupling with a diverse range of primary/secondary amines, to generate intermediates 43.
  • Acid mediated deprotection reaction gave compounds, Structure XVI.
  • intermediates 43 were separated by chiral HPLC/SFC to generate two enantiomers. The resulting intermediates were deprotected using acidic conditions, to generate the enantiomers of Structure XVI. Second generation synthesis of intermediates 41 Scheme 21.
  • Second generation synthesis of intermediates 41 (as in Scheme 20).
  • the first step of the synthesis involved a palladium-mediated Suzuki-Miyaura coupling reaction to introduce a vinyl substituent on intermediate 44 to generate intermediate 45.
  • Intermediate 45 is subjected to oxidation to generate aldehyde intermediates 46.
  • the final step of the synthesis involved an oxidative intermolecular cyclization between intermediates 46 and intermediate 3 to give ester intermediates 41.
  • Alternative synthesis of intermediates 46 Scheme 22.
  • Alternative synthesis of intermediates 46 (as in Scheme 21).
  • This step of the synthesis involved oxidation of benzyl alcohol intermediates 47 using Dess- Martin periodinane or other oxidants to generate aldehyde intermediates 46.
  • the first step of the synthesis involved reaction of 5-fluoroisobenzofuran-1,3-dione in formamide at elevated temperaturess affording 5-fluoroisoindoline-1,3-dione intermediate 33.
  • Intermediate 33 was subjected to regioselective nitration to generate intermediate 35.
  • the nitro group was reduced using 10% palladium on activated carbon to give intermediate 36.
  • Intermediate 36 was treated with t-butyl nitrite and copper(I) bromide to generate intermediate 37.
  • the final step of the synthesis involved reduction of intermediate 37 with diborane in THF at elevated temperatures following by in-situ Boc protection affording intermediate 38 (Scheme 30).
  • Scheme 31 Synthesis of functionalized Anologues 45.
  • N-Boc protecting group was removed by 4 N hydrochloride in 1,4-dioxane or by trifluoroacetic acid to generate benzo[d]imidazo[2,1-b]thiazole-7-carboxamide analogues 10 as a free base or as the hydrochloride/formic acid salt.
  • Chiral resolution was performed on N-Boc protected compounds 9 to generate, after subsequent N-Boc protecting group removal, the individual enantiomers if required.
  • Imidazole intermediate 45 (Scheme 41) was synthesized from commercially available 4-bromo- 3-fluorobenzaldehyde via a cyclization reaction. The imidazole was protected with a SEM group to generate intermediate 46.
  • Scheme 42 General synthesis of right-hand side fragment bromobenzene analogue 49.
  • Scheme 43 The pyrazole was protected with a SEM group to generate intermediate 49.
  • the ketone intermediate 64 was synthesized following the synthetic procedure described in Scheme 32 Step 1. Ketone reduction gave the alcohol intermediate 65. A Mitsunobu reaction was performed on 65 using the reagent CMBP to selectively generate trans intermediate 66. The TBDPS group was removed by reaction with TBAF to generate intermediate 67. Scheme 49. General synthesis of right-hand side fragment boronic esters/acids analogues 68. [00298] Bromobenzene analogues I (Scheme 49) were converted to their corresponding boronic esters/acids analogues 68 via Miyaura borylation reaction.
  • Scheme 50 General synthesis of right-hand side modified benzo[d]imidazo[2,1-b]thiazole-7-carboxamide analogues 74. [00299] Alkylation of commercially available ethyl 2-aminobenzothiazole-6-carboxylate (Scheme 50) with tert-butyl bromoacetate at elevated temperature afforded intermediate 69. The tert-butyl ester was hydrolyzed using a mixture of TFA-DCM to generate the carboxylic acid intermediate 70.
  • N-Boc protecting group was removed by 4 N hydrochloride in 1,4-dioxane to generate benzo[d]imidazo[2,1-b]thiazole-7-carboxamide analogues 74 as the free base or as the hydrochloride salt.
  • Chiral resolution was performed on N-Boc protected compounds 73 to generate, after subsequent N-Boc protecting group removal, the individual enantiomers if required.
  • Scheme 51 General synthesis of right-hand side modified benzo[d]imidazo[2,1-b]thiazole-7-carboxamide analogues 76.
  • the ketone of intermediate 73 (Scheme 51) was reduced by sodium borohydride to generate alcohol intermediate 75.
  • the N-Boc protecting group was removed by 4 N hydrochloride in 1,4-dioxane to generate benzo[d]imidazo[2,1-b]thiazole-7-carboxamide analogues 76 as the free base or as the hydrochloride salt.
  • Scheme 52 General synthesis of right-hand side modified benzo[d]imidazo[2,1-b]thiazole-7-carboxamide analogues 78.
  • Difluoro intermediate 77 (Scheme 52) was synthesized from ketone intermediate 73 by reaction with DAST reagent. The N-Boc protecting group was removed by 4 N hydrochloride in 1,4-dioxane to generate benzo[d]imidazo[2,1-b]thiazole-7-carboxamide analogues 78 as the free base or as the hydrochloride salt.
  • Scheme 54 General synthesis of benzo[d]imidazo[2,1-b]thiazole-7-carboxamide analogue 85.
  • the hydroxyl group of intermediate 73 was converted to fluoride using DAST reagent, to generate intermediate 84.
  • the N-Boc protecting group was removed by treatment with 4 N hydrochloride in 1,4-dioxane, to generate benzo[d]imidazo[2,1-b]thiazole-7-carboxamide analogues 85 as a free base or as the hydrochloride salt.
  • Scheme 55 General synthesis of benzo[d]imidazo[2,1-b]thiazole-7-carboxamide analogue 89.
  • N-THP protecting group was removed by 4 N hydrochloride in 1,4- dioxane to generate benzo[d]imidazo[2,1-b]thiazole-7-carboxamide analogue 98 as a free base or as the hydrochloride salt.
  • the reaction solution was stirred for 3 h at room temperature under a nitrogen atmosphere and was purified by reverse phase flash chromatography with the following conditions: Column: Spherical C18, 20 - 40 um, 120 g; Mobile Phase A: water (10 mM NH4HCO3); Mobile Phase B: acetonitrile; Flow rate: 80 mL/min; Gradient: 40% B - 60% B in 20 min; Detector: 254 nm.
  • reaction solution was warmed to room temperature and stirred for 16 h.
  • di-tert-butyl dicarbonate 35.32 g, 161.83 mmol
  • the reaction mixure was concentrated under reduced pressureto give the crude residue, which was purified by reverse phase flash chromatography using the following conditions: Column: Spherical C18, 20-40 ⁇ m, 330 g; Mobile Phase A: water (plus 10 mmol/L ammonium bicarbonate); Mobile Phase B: acetonitrile; Flow rate: 80 mL/min; Gradient: 75%-95% B in 20 min; Detector: UV 254/220 nm.
  • reaction mixture was acidified to pH 6 with 2 N hydrochloric acid solution.
  • the solids were collected by filtration, washed with water (3 x 10 mL) 5nd oven dried to afford 2-(4-(1-(tert- butoxycarbonyl)pyrrolidin-2-yl)-2-fluorophenyl)benzo[d]imidazo[2,1-b]thiazole-7-carboxylic acid as a white solid. Yield 1.50 g (72%).
  • tert-butyl (4-(4-bromo-2,3-difluorophenyl)-4-oxobutyl)carbamate Compound tert-butyl (4-(4-bromo-2,3-difluorophenyl)-4-oxobutyl)carbamate was prepared from 1,4-dibromo-2,3-difluorobenzene (5.00 g, 18.39 mmol) and tert-butyl 2-oxopyrrolidine-1- carboxylate (4.43 g, 23.92 mmol), following a similar procedure to that described for the synthesis of tert-butyl (4-(4-bromo-3-fluorophenyl)-4-oxobutyl)carbamate and was isolated as a yellow oil.
  • reaction mixture was diluted with water (200 mL) and extracted with dichloromethane (3 x 500 mL). The combined organic layers were washed with brine (3 x 200 mL) and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluted with 0-70% ethyl acetate in petroleum ether) to afford 1- (4-bromo-3-fluorophenyl)cyclopropane-1-carbonitrile as a pink solid. Yield 21.00 g (75%).
  • reaction solution was purified directly by silica gel column chromatography (eluted with 0-70% ethyl acetate in petroleum ether) to afford tert-butyl (1-(4-bromo-3- fluorophenyl)cyclopropyl)carbamate as a white solid. Yield 0.40 g (31%).
  • the reaction mixture was stirred for 4 h at 70°C.
  • the mixture was cooled to room temperature, diluted with water (500 mL) and extracted with ethyl acetate (3 x 300 mL).
  • the combined organic layers were washed with brine (300 mL) and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure.
  • the residue was purified by silica gel column chromatography (25% ethyl acetate in petroleum ether) to afford tert-butyl 4-(4-bromo-3- fluorophenyl)-3,6-dihydropyridine-1(2H)-carboxylate as a white oil. Yield 16.00 g (90%).
  • tert-butyl (5-(4-bromo-3-fluorophenyl)-5-oxopentyl)carbamate [00390] Compound tert-butyl (5-(4-bromo-3-fluorophenyl)-5-oxopentyl)carbamate was prepared from 1-bromo-2-fluoro-4-iodobenzene (10.00 g, 33.23 mmol) and tert-butyl 2-oxopiperidine-1-carboxylate (8.00 g, 40.15 mmol), following a similar procedure to that described for the synthesis of tert-butyl (4- (4-bromo-3-fluorophenyl)-4-oxobutyl)carbamate and was isolated as a white solid.
  • reaction mixture was treated with (2-(chloromethoxy)ethyl)trimethylsilane (838 mg, 5.026 mmol).
  • the reaction was warmed to room temperature and stirred for an additional 2 h.
  • the reaction was quenched by the addition of saturated aqueous ammonium chloride (30 mL).
  • the resulting mixture was extracted with ethyl acetate (3 x 30 mL).
  • the combined organic layers were dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure.
  • the reaction mixture was diluted with water (200 mL) and extracted with ethyl acetate (3 x 200 mL). The combined organic layers were washed with brine (100 mL) and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluted with 0-10% ethyl acetate in petroleum ether) to afford tert-butyl 3-(4-bromo-3-fluorophenyl)morpholine-4- carboxylate as a colorless oil. Yield 320 mg (27%).
  • reaction solution was stirred for 3 h.
  • the reaction solution was purified directly by Prep-TLC (eluted with 9% methanol in dichloromethane) to afford tert-butyl 4,4-difluoro-2- (3-fluoro-4-(7-((3-(4-fluoropiperidin-1-yl)propyl)carbamoyl)benzo[d]imidazo[2,1-b]thiazol-2- yl)phenyl)pyrrolidine-1-carboxylate as a white solid. Yield 35 mg (34%). 1 H NMR not run. m/z: [ESI + ] 660 (M+H) + .
  • the reaction solution was warmed to room temperature and stirred for an additional 1 h.
  • the reaction was quenched with water (2 mL) at 0°C.
  • the resulting mixture was concentrated under reduced pressure.
  • the residue was purified by reverse phase flash chromatography using the following conditions; Column, Spherical C18, 20-40 ⁇ m, 330 g; Mobile Phase A: water (plus 10 mmol/L ammonium bicarbonate); Mobile Phase B; acetonitrile; Flow rate: 80 mL/min; Gradient:45%-65% B in 20 min; UV Detector: 254 nm.
  • reaction solution was stirred for 16 h.
  • the reaction mixture was concentrated under reduced pressure.
  • the residue was purified by silica gel column chromatography (eluted with 30% ethyl acetate in petroleum ether) to afford tert- butyl 4-((tert-butyldiphenylsilyl)oxy)-2-oxopyrrolidine-1-carboxylate as a colorless oil. Yield 25.00 g (97%).
  • the reaction mixture was stirred for 16 h at 120°C.
  • the mixture was cooled to room temperature and filtered.
  • the filter cake was washed with ethyl acetate (3 x 10 mL).
  • the combined filtrates were diluted with brine (100 mL) and extracted with ethyl acetate (2 x 50 mL).
  • the combined organic layers were washed with brine (100 mL) and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure.
  • the reaction solution was concentrated under reduced pressure.
  • the residue was purified by Prep-HPLC using the following conditions; Column: XBridge Prep OBD C18 Column, 30 x 150 mm, 5 ⁇ m; Mobile Phase A: water (plus 10 mmol/L ammonium bicarbonate), Mobile Phase B: acetonitrile; Flow rate: 60 mL/min mL/min; Gradient: 12%-22% B in 7.8 min; UV Detector: 254nm/220nm nm.

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Abstract

La présente invention concerne de nouveaux modulateurs de la traduction d'ARNm de c-MYC, une composition et des procédés de préparation de ceux-ci, et leurs utilisations dans le traitement du cancer.
EP23836030.9A 2022-07-03 2023-07-02 Modulateurs de la traduction d'arnm de c-myc et leurs utilisations dans le traitement du cancer Pending EP4547672A1 (fr)

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US17/856,998 US20220370431A1 (en) 2021-01-05 2022-07-03 C-myc mrna translation modulators and uses thereof in the treatment of cancer
PCT/US2023/026828 WO2024010762A1 (fr) 2022-07-03 2023-07-02 Modulateurs de la traduction d'arnm de c-myc et leurs utilisations dans le traitement du cancer

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AU2023305002A1 (en) 2024-11-14
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