ES2328820T3 - Derivados de 4-(pirazol-3-ilamino)pirimidina para uso en el tratamiento de cancer. - Google Patents
Derivados de 4-(pirazol-3-ilamino)pirimidina para uso en el tratamiento de cancer. Download PDFInfo
- Publication number
- ES2328820T3 ES2328820T3 ES04768838T ES04768838T ES2328820T3 ES 2328820 T3 ES2328820 T3 ES 2328820T3 ES 04768838 T ES04768838 T ES 04768838T ES 04768838 T ES04768838 T ES 04768838T ES 2328820 T3 ES2328820 T3 ES 2328820T3
- Authority
- ES
- Spain
- Prior art keywords
- alkyl
- cycloalkyl
- alkoxy
- ring
- amino
- 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.)
- Expired - Lifetime
Links
- 206010028980 Neoplasm Diseases 0.000 title 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 title 1
- 201000011510 cancer Diseases 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 19
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 9
- 229910052736 halogen Inorganic materials 0.000 abstract 9
- 150000002367 halogens Chemical class 0.000 abstract 9
- 229910052757 nitrogen Inorganic materials 0.000 abstract 9
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 7
- 125000005842 heteroatom Chemical group 0.000 abstract 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 7
- 229910052760 oxygen Inorganic materials 0.000 abstract 7
- 239000001301 oxygen Chemical group 0.000 abstract 7
- 125000001424 substituent group Chemical group 0.000 abstract 7
- 229910052717 sulfur Chemical group 0.000 abstract 7
- 239000011593 sulfur Chemical group 0.000 abstract 7
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 6
- 125000002950 monocyclic group Chemical group 0.000 abstract 6
- -1 (C3-C8) -carbonyl Chemical group 0.000 abstract 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 5
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 5
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000000623 heterocyclic group Chemical group 0.000 abstract 3
- 229920006395 saturated elastomer Polymers 0.000 abstract 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 abstract 2
- 150000002431 hydrogen Chemical group 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 1
- DROZYMFJWSYDRY-UHFFFAOYSA-N 2,7-diazaspiro[3.5]nonane Chemical group C1NCC11CCNCC1 DROZYMFJWSYDRY-UHFFFAOYSA-N 0.000 abstract 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000003830 C1- C4 alkylcarbonylamino group Chemical group 0.000 abstract 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 1
- 125000005236 alkanoylamino group Chemical group 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000005115 alkyl carbamoyl group Chemical group 0.000 abstract 1
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 1
- 125000001589 carboacyl group Chemical group 0.000 abstract 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 abstract 1
- 125000006413 ring segment Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/10—Drugs for disorders of the urinary system of the bladder
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/10—Spiro-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Urology & Nephrology (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Gastroenterology & Hepatology (AREA)
- Oncology (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Diabetes (AREA)
- Reproductive Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Peptides Or Proteins (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Un compuesto de fórmula (I) **(Ver fórmula)** o una de sus sales farmacéuticamente aceptable, en la que: R1 representa trifluorometilo, o un alquilo (C1-C6), cicloalquilo (C3-C8) o cicloalquil (C3-C8)-alquilo (C1-C6), cada uno de cuyos grupos puede estar opcionalmente sustituido por uno o más sustituyentes independientemente seleccionados entre halógeno y alcoxi (C1-C6); R2 representa hidrógeno, halógeno o trifluorometilo; R3 representa hidrógeno, hidroxilo o halógeno, o un grupo alquilo (C1-C6), alquenilo (C2-C6), alquinilo (C2-C6), cicloalquilo (C3-C8), cicloalquil (C3-C8)-alquilo (C1-C6), alcoxi (C1-C6), cicloalquil (C3-C8)-alcoxi (C1-C6), alquil (C1-C6)-carbonilo, cicloalquil (C3-C8)-carbonilo, cicloalquil (C3-C8)-alquil (C1-C6)-carbonilo, alcoxi (C1-C6)- carbonilo, amino, alquil (C1-C6)-amino, di-[alquil (C1-C6)]amino, cicloalquil (C3-C8)-amino, cicloalquil (C3-C8)- alquil (C1-C6)-amino, alcoxi (C1-C6)-amino, carbamoilo, alquil (C1-C6)-carbamoilo, di-[alquil (C1-C6)]carbamoilo, -C(O)R3b, -OR3b, -SR3b, -NHR3b, -N[alquil (C1-C6)]R3b, -S(O)mR3a o -N(R3c)C(O)R3a, en el que R3a representa un grupo alquilo (C1-C6), cicloalquilo (C3-C8), cicloalquil (C3-C8)-alquilo (C1-C6) o alcoxi (C1-C6), m es 0, 1 ó 2, R3b representa un anillo heterocíclico de 4, 5 ó 6 miembros monocíclico saturado que comprende al menos un heteroátomo de anillo seleccionado entre nitrógeno, oxígeno y azufre y R3c representa hidrógeno o alquilo (C1-C6), o R3 representa un anillo heterocíclico de 5 ó 6 miembros, monocíclico, saturado, que comprende al menos un heteroátomo de anillo seleccionado entre nitrógeno, oxígeno y azufre, o R3 representa un anillo heteroaromático de 5 ó 6 miembros que comprende al menos un heteroátomo de anillo seleccionado entre nitrógeno, oxígeno y azufre, o R3 representa un grupo 2,7-diazaspiro[3.5]nonano, cada uno de cuyos grupos o anillos en R3 puede estar opcionalmente sustituido por uno o más sustituyentes independientemente seleccionados entre alquilo (C1-C6), alcoxi (C1-C6), alcoxi (C1-C6)-alquilo (C1-C6), alcoxi (C1- C6)-alcoxi (C1-C6), halógeno, hidroxilo, trifluorometilo, tri-[alquil (C1-C4)]sililo, ciano, amino, alquil (C1-C6)-amino, di-[alquil (C1-C6)]-amino, cicloalquil (C3-C8)-amino, cicloalquil (C3-C6)-alquil (C1-C3)-amino, aminoalquilo (C1-C6), alquil (C1-C6)-aminoalquilo (C1-C6), di-[alquil (C1-C6)]-aminoalquilo (C1-C6), cicloalquil (C3-C8)-aminoalquilo (C1-C6), cicloalquil (C3-C6)-alquil (C1-C3)-aminoalquilo (C1-C6), alcoxi (C1-C6)-carbonilo, carbamoilo, alquil (C1-C6)-carbamoilo, di-[alquil (C1-C6)]carbamoilo, alquil (C1-C6)-tio, alquil (C1-C6)-sulfonilo, alquil (C1- C6)-sulfinilo, alcanoilo (C1-C6), un grupo alcanoilamino -N(R3c)C(O)R3a en el que R3a y R3c son como se define antes, o un anillo de 3, 4, 5, 6 ó 7 miembros, monocíclico, saturado, cuyo anillo puede comprender opcionalmente uno o más heteroátomos seleccionados entre nitrógeno, oxígeno y azufre, cualquiera de cuyos sustituyentes puede estar opcionalmente sustituido por uno o más grupos alquilo (C1-C4), hidroxilo o ciano; -NQ1 representa un anillo de 5 a 6 miembros, monocíclico, saturado unido a N que contiene un heteroátomo de nitrógeno y que comprende opcionalmente uno o más heteroátomos de anillo adicionales seleccionados entre nitrógeno, oxígeno y azufre; Q2 representa un anillo heteroaromático de 5 ó 6 miembros que comprende al menos un heteroátomo de anillo seleccionado entre nitrógeno, oxígeno y azufre, cuyo anillo está sustituido por Q3 y está opcionalmente sustituido, sobre cualquier átomo de anillo disponible, por uno o más sustituyentes diferentes independientemente seleccionados entre alquilo (C1-C6) o alcoxi (C1-C6) (cualquiera de ellos puede estar opcionalmente sustituido por uno o más sustituyentes independientemente seleccionados entre halógeno, amino, hidroxilo y trifluorometilo), halógeno, nitro, ciano, -NR4R5, carboxilo, hidroxilo, alquenilo (C2-C6), cicloalquilo (C3-C8), cicloalquil (C3-C8)-alquilo (C1-C6), alcoxi (C1-C4)-carbonilo, alquil (C1-C4)-carbonilo, alquil (C1-C4)-carbonilamino, fenilcarbonilo, -S(O)palquilo (C1-C4), -C(O)NR6R7 y -SO2NR8R9, en el que R4, R5, R6, R7, R8 y R9 representan cada uno independientemente hidrógeno o alquilo (C1-C6), o R4 y R5, o R6 y R7, o R8 y R9, cuando se toman junto con el átomo de nitrógeno al que están unidos, pueden formar cada uno independientemente un anillo heterocíclico saturado y p es 0, 1 ó 2; Q3 representa un grupo alquilo (C1-C6), cicloalquilo (C3-C6) o cicloalquil (C3-C6)-alquilo (C1-C6) o un anillo, monocíclico, de 5 a 6 miembros saturado o insaturado que puede comprender al menos un heteroátomo de anillo seleccionado entre nitrógeno, oxígeno y azufre, y en el que Q3 está opcionalmente sustituido por uno o más sustituyentes independientemente seleccionados entre alquilo (C1-C6) o alcoxi (C1-C6) (cualquiera de ellos puede estar opcionalmente sustituido por uno o más sustituyentes independientemente seleccionados entre halógeno, amino, hidroxilo y trifluorometilo), halógeno, nitro, ciano, -NR10R11, carboxilo, hidroxilo, alquenilo (C2-C6), cicloalquilo (C3-C8), alcoxi (C1-C6)-carbonilo, alquil (C1-C6)-carbonilo, alquil (C1-C6)-carbonilamino, fenilcarbonilo, -S(O)nalquilo (C1- C6), -C(O)NR12R13 y -SO2NR14R15, en el que R10, R11, R12, R13, R14 y R15 representan cada uno independientemente hidrógeno o alquilo (C1-C6), o R10 y R11, o R12 y R13, o R14 y R15, cuando se toman junto con el átomo de nitrógeno al que están unidos, pueden formar cada uno independientemente un anillo heterocíclico saturado y n es 0, 1 ó 2; y en el que cualquier anillo monocíclico, saturado, lleva opcionalmente 1 ó 2 sustituyentes oxo o tioxo. 2. Un compuesto de acuerdo con l
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0324335A GB0324335D0 (en) | 2003-10-17 | 2003-10-17 | Novel compounds |
| GB0324335 | 2003-10-17 | ||
| GB0412194 | 2004-06-02 | ||
| GB0412194A GB0412194D0 (en) | 2004-06-02 | 2004-06-02 | Novel compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2328820T3 true ES2328820T3 (es) | 2009-11-18 |
Family
ID=34525049
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES04768838T Expired - Lifetime ES2328820T3 (es) | 2003-10-17 | 2004-10-11 | Derivados de 4-(pirazol-3-ilamino)pirimidina para uso en el tratamiento de cancer. |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US7579349B2 (es) |
| EP (1) | EP1678169B1 (es) |
| JP (1) | JP2007510626A (es) |
| KR (1) | KR20060123164A (es) |
| AR (1) | AR046338A1 (es) |
| AU (1) | AU2004283137A1 (es) |
| BR (1) | BRPI0415398A (es) |
| CA (1) | CA2542522A1 (es) |
| DE (1) | DE602004022187D1 (es) |
| ES (1) | ES2328820T3 (es) |
| IL (1) | IL174989A0 (es) |
| NO (1) | NO20062130L (es) |
| SA (1) | SA04250338B1 (es) |
| TW (1) | TW200530229A (es) |
| UY (1) | UY28565A1 (es) |
| WO (1) | WO2005040159A1 (es) |
Families Citing this family (60)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1317450B1 (en) | 2000-09-15 | 2006-11-22 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
| US6660731B2 (en) | 2000-09-15 | 2003-12-09 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
| WO2004072029A2 (en) | 2003-02-06 | 2004-08-26 | Vertex Pharmaceuticals Incorporated | Pyrazolopyridazines useful as inhibitors of protein kinases |
| WO2005061519A1 (en) | 2003-12-19 | 2005-07-07 | Takeda San Diego, Inc. | Kinase inhibitors |
| RU2381226C2 (ru) * | 2004-02-18 | 2010-02-10 | Астразенека Аб | Полигетероциклические соединения и их применение в качестве антагонистов метаботропного рецептора глутамата |
| EP1778669A2 (en) | 2004-08-18 | 2007-05-02 | Takeda San Diego, Inc. | Kinase inhibitors |
| ATE479687T1 (de) | 2004-10-15 | 2010-09-15 | Takeda Pharmaceutical | Kinaseinhibitoren |
| JP2008520713A (ja) | 2004-11-17 | 2008-06-19 | ミイカナ セラピューティクス インコーポレイテッド | キナーゼ阻害剤 |
| AU2005322855B2 (en) | 2004-12-30 | 2012-09-20 | Exelixis, Inc. | Pyrimidine derivatives as kinase modulators and method of use |
| JP2008534481A (ja) * | 2005-03-23 | 2008-08-28 | アストラゼネカ アクチボラグ | インスリン様増殖因子−1受容体活性の阻害剤としての2−アゼチジニル−4−(1h−ピラゾール−3−イルアミノ)ピリミジン |
| SI1869032T1 (sl) * | 2005-04-05 | 2008-12-31 | Astrazeneca Ab | Pirimidinski derivati za uporabo kot sredstva proti raku |
| GB0506886D0 (en) * | 2005-04-05 | 2005-05-11 | Astrazeneca Ab | Chemical compounds |
| WO2007023382A2 (en) * | 2005-08-25 | 2007-03-01 | Pfizer Inc. | Pyrimidine amino pyrazole compounds, potent kinase inhibitors |
| US20090306116A1 (en) * | 2005-09-16 | 2009-12-10 | Astrazeneca Ab | Pyrimidine derivatives for the inhibition of igf-ir tyrosine kinase activity |
| CA2622352C (en) * | 2005-09-30 | 2014-05-27 | Miikana Therapeutics, Inc. | Substituted pyrazole compounds |
| US8119655B2 (en) | 2005-10-07 | 2012-02-21 | Takeda Pharmaceutical Company Limited | Kinase inhibitors |
| EP1954277B1 (en) | 2005-11-03 | 2017-01-18 | Vertex Pharmaceuticals Incorporated | Aminopyrimidines useful as kinase inhibitors |
| CA2629781A1 (en) * | 2005-11-16 | 2007-05-24 | Vertex Pharmaceuticals Incorporated | Aminopyrimidines useful as kinase inhibitors |
| AU2007244183B2 (en) * | 2006-04-27 | 2012-05-10 | Msd K.K. | Novel aminopyridine derivative having aurora-a-selective inhibitory activity |
| JP2009541480A (ja) * | 2006-06-30 | 2009-11-26 | アストラゼネカ アクチボラグ | 癌の治療において有用なピリミジン誘導体 |
| EP2043651A2 (en) | 2006-07-05 | 2009-04-08 | Exelixis, Inc. | Methods of using igf1r and abl kinase modulators |
| SG158147A1 (en) | 2006-10-09 | 2010-01-29 | Takeda Pharmaceutical | Kinase inhibitors |
| MX2009004807A (es) | 2006-11-02 | 2009-06-15 | Vertex Pharma | Aminopiridinas y aminopirimidinas utiles como inhibidores de proteina cinasa. |
| NZ577768A (en) * | 2006-12-19 | 2012-01-12 | Vertex Pharma | Aminopyrimidines useful as inhibitors of protein kinases |
| ATE526328T1 (de) * | 2007-03-09 | 2011-10-15 | Vertex Pharma | Als inhibitoren von proteinkinasen geeignete aminopyrimidine |
| MX2009009592A (es) | 2007-03-09 | 2009-11-10 | Vertex Pharma | Aminopiridinas utiles como inhibidores de proteinas cinasas. |
| MX2009009590A (es) | 2007-03-09 | 2009-11-10 | Vertex Pharma | Aminopirimidinas utiles como inhibidores de proteinas cinasas. |
| WO2008117051A1 (en) * | 2007-03-27 | 2008-10-02 | Astrazeneca Ab | S-6-meth0xy-2- (2- (3- (pyrimid-2-yl) is0xaz0l-5-yl) pyrrolidin-1-yl) -4- (5-methyl-ih-pyrazol-s-ylamino) pyrimidine and polymorphic forms thereof as modulators of the insulin-like growth |
| AU2008240313A1 (en) | 2007-04-13 | 2008-10-23 | Aj Park | Aminopyrimidines useful as kinase inhibitors |
| JP5389786B2 (ja) | 2007-05-02 | 2014-01-15 | バーテックス ファーマシューティカルズ インコーポレイテッド | キナーゼ阻害として有用なアミノピリミジン |
| AU2008247592A1 (en) | 2007-05-02 | 2008-11-13 | Vertex Pharmaceuticals Incorporated | Thiazoles and pyrazoles useful as kinase inhibitors |
| AU2008262291A1 (en) * | 2007-06-11 | 2008-12-18 | Miikana Therapeutics, Inc. | Substituted pyrazole compounds |
| CN101790532B (zh) | 2007-07-31 | 2013-11-20 | 沃泰克斯药物股份有限公司 | 5-氟-1H-吡唑并[3,4-b]吡啶-3-胺及其衍生物的制备方法 |
| WO2009019518A1 (en) * | 2007-08-09 | 2009-02-12 | Astrazeneca Ab | Pyrimidine compounds having a fgfr inhibitory effect |
| US8278313B2 (en) | 2008-03-11 | 2012-10-02 | Abbott Laboratories | Macrocyclic spiro pyrimidine derivatives |
| US8436005B2 (en) | 2008-04-03 | 2013-05-07 | Abbott Laboratories | Macrocyclic pyrimidine derivatives |
| WO2010111050A1 (en) * | 2009-03-23 | 2010-09-30 | Banyu Pharmaceutical Co., Ltd. | Novel aminopyridine derivatives having aurora a selective inhibitory action |
| JP2012521426A (ja) * | 2009-03-24 | 2012-09-13 | Msd株式会社 | オーロラa選択的阻害作用を有する新規アミノピリジン誘導体 |
| US20110053916A1 (en) * | 2009-08-14 | 2011-03-03 | Vertex Pharmaceuticals Incorporated | Pyrimidine compounds as tuberculosis inhibitors |
| MX2012007200A (es) | 2009-12-21 | 2012-07-10 | Bayer Cropscience Ag | Bis(difluorometil)pirazoles como fungicidas. |
| US20120122928A1 (en) | 2010-08-11 | 2012-05-17 | Bayer Cropscience Ag | Heteroarylpiperidine and -Piperazine Derivatives as Fungicides |
| EP2423210A1 (de) | 2010-08-25 | 2012-02-29 | Bayer CropScience AG | Heteroarylpiperidin- und -piperazinderivate als Fungizide |
| US8759527B2 (en) | 2010-08-25 | 2014-06-24 | Bayer Cropscience Ag | Heteroarylpiperidine and -piperazine derivatives as fungicides |
| EP2632922B1 (de) | 2010-10-27 | 2019-02-27 | Bayer CropScience Aktiengesellschaft | Heteroarylpiperidin und -piperazinderivate als fungizide |
| WO2012104273A1 (de) | 2011-02-01 | 2012-08-09 | Bayer Cropscience Ag | Heteroarylpiperidin und -piperazinderivate als fungizide |
| EP2532233A1 (en) | 2011-06-07 | 2012-12-12 | Bayer CropScience AG | Active compound combinations |
| US10004232B2 (en) | 2011-09-15 | 2018-06-26 | Bayer Intellectual Property Gmbh | Piperidine pyrazoles as fungicides |
| DK2797899T3 (en) | 2011-12-27 | 2016-04-04 | Bayer Ip Gmbh | Heteroarylpiperidin and -piperazinderivater as fungicides |
| EP3241830A1 (de) | 2016-05-04 | 2017-11-08 | Bayer CropScience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| TW201838974A (zh) | 2017-04-19 | 2018-11-01 | 印度商Pi工業公司 | 具殺菌性質之雜環化合物 |
| EP3820500A4 (en) * | 2018-07-13 | 2022-04-13 | Teqla Therapeutics, Inc. | USE OF BCL6 INHIBITORS FOR THE TREATMENT OF AUTOIMMUNE DISEASES |
| UY38940A (es) | 2019-11-11 | 2021-06-30 | Pi Industries Ltd | Nuevas piridiniloxi piperidiniletanonas sustituidas |
| UY38941A (es) | 2019-11-11 | 2021-06-30 | Pi Industries Ltd | Nuevas sulfiliminas o sulfoximinas que contienen compuestos heterocíclicos fungicidas |
| AR120376A1 (es) | 2019-11-11 | 2022-02-09 | Pi Industries Ltd | Heteroaril piperidiniletanonas sustituidas con actividad fungicida |
| TWI906428B (zh) | 2020-12-10 | 2025-12-01 | 南韓商Lg化學股份有限公司 | 酸(Boronic Acid)化合物 |
| WO2022211595A1 (ko) * | 2021-04-01 | 2022-10-06 | 주식회사 엘지화학 | 옥사디아졸 화합물 및 이를 포함하는 약제학적 조성물 |
| CN117794527A (zh) * | 2021-06-04 | 2024-03-29 | 学校法人京都药科大学 | 新型活化amp的蛋白激酶活化剂 |
| WO2023163712A1 (en) * | 2022-02-25 | 2023-08-31 | Nalo Therapeutics | Modulators of myc family proto-oncogene protein |
| TW202348225A (zh) * | 2022-02-25 | 2023-12-16 | 美商納羅醫療公司 | Myc家族原癌基因蛋白之調節劑 |
| GB2630970A (en) * | 2023-06-15 | 2024-12-18 | Duke Street Bio Ltd | PARP1 inhibitor compounds |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2426180A1 (de) | 1974-05-29 | 1975-12-18 | Bayer Ag | Verfahren zum faerben von polyurethankunststoffen |
| GB9523675D0 (en) | 1995-11-20 | 1996-01-24 | Celltech Therapeutics Ltd | Chemical compounds |
| ES2274634T3 (es) | 1998-08-29 | 2007-05-16 | Astrazeneca Ab | Compuestos de pirimidina. |
| US6337338B1 (en) | 1998-12-15 | 2002-01-08 | Telik, Inc. | Heteroaryl-aryl ureas as IGF-1 receptor antagonists |
| GB9828511D0 (en) | 1998-12-24 | 1999-02-17 | Zeneca Ltd | Chemical compounds |
| DE19917785A1 (de) | 1999-04-20 | 2000-10-26 | Bayer Ag | 2,4-Diamino-pyrimidin-Derivate |
| CA2384188C (en) | 1999-09-24 | 2008-06-17 | Janssen Pharmaceutica N.V. | Antiviral compositions |
| EP1257546A1 (en) | 2000-02-17 | 2002-11-20 | Amgen Inc. | Kinase inhibitors |
| GB0004887D0 (en) | 2000-03-01 | 2000-04-19 | Astrazeneca Uk Ltd | Chemical compounds |
| GB0004890D0 (en) | 2000-03-01 | 2000-04-19 | Astrazeneca Uk Ltd | Chemical compounds |
| JP4969010B2 (ja) | 2000-05-08 | 2012-07-04 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Hiv複製阻害性ピリミジンのプロドラッグ |
| EP1317450B1 (en) | 2000-09-15 | 2006-11-22 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
| NZ526472A (en) | 2000-12-21 | 2004-04-30 | Vertex Pharma | Pyrazole compounds useful as protein kinase inhibitors |
| SE0104140D0 (sv) | 2001-12-07 | 2001-12-07 | Astrazeneca Ab | Novel Compounds |
-
2004
- 2004-10-11 WO PCT/GB2004/004307 patent/WO2005040159A1/en not_active Ceased
- 2004-10-11 JP JP2006534814A patent/JP2007510626A/ja active Pending
- 2004-10-11 KR KR1020067009627A patent/KR20060123164A/ko not_active Withdrawn
- 2004-10-11 EP EP04768838A patent/EP1678169B1/en not_active Expired - Lifetime
- 2004-10-11 CA CA002542522A patent/CA2542522A1/en not_active Abandoned
- 2004-10-11 US US10/595,390 patent/US7579349B2/en not_active Expired - Fee Related
- 2004-10-11 DE DE602004022187T patent/DE602004022187D1/de not_active Expired - Lifetime
- 2004-10-11 AU AU2004283137A patent/AU2004283137A1/en not_active Abandoned
- 2004-10-11 BR BRPI0415398-7A patent/BRPI0415398A/pt not_active IP Right Cessation
- 2004-10-11 ES ES04768838T patent/ES2328820T3/es not_active Expired - Lifetime
- 2004-10-14 TW TW093131214A patent/TW200530229A/zh unknown
- 2004-10-15 UY UY28565A patent/UY28565A1/es not_active Application Discontinuation
- 2004-10-15 AR ARP040103757A patent/AR046338A1/es unknown
- 2004-10-16 SA SA04250338A patent/SA04250338B1/ar unknown
-
2006
- 2006-04-11 IL IL174989A patent/IL174989A0/en unknown
- 2006-05-12 NO NO20062130A patent/NO20062130L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| IL174989A0 (en) | 2006-08-20 |
| EP1678169B1 (en) | 2009-07-22 |
| KR20060123164A (ko) | 2006-12-01 |
| NO20062130L (no) | 2006-05-12 |
| JP2007510626A (ja) | 2007-04-26 |
| US7579349B2 (en) | 2009-08-25 |
| WO2005040159A1 (en) | 2005-05-06 |
| SA04250338B1 (ar) | 2008-11-18 |
| TW200530229A (en) | 2005-09-16 |
| US20070037888A1 (en) | 2007-02-15 |
| AU2004283137A1 (en) | 2005-05-06 |
| CA2542522A1 (en) | 2005-05-06 |
| UY28565A1 (es) | 2005-05-31 |
| EP1678169A1 (en) | 2006-07-12 |
| AR046338A1 (es) | 2005-12-07 |
| BRPI0415398A (pt) | 2006-12-19 |
| DE602004022187D1 (de) | 2009-09-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES2328820T3 (es) | Derivados de 4-(pirazol-3-ilamino)pirimidina para uso en el tratamiento de cancer. | |
| AR046779A1 (es) | Derivados de pirazol, metodos para su preparacion y usos de los mismos en la fabricacion de composiciones farmaceuticas y medicamentos que los contienen con actividad inhibitoria de trk para el tratamiento o profilaxis del cancer. | |
| ECSP105253A (es) | Derivados de 5-feniltiazol y uso como inhibidores de pi3 cinasa | |
| AR055592A1 (es) | Derivados de 2-amino-5-cicloalquil-hidantoina como moduladores y/o inhibidores de la beta-secretasa(bace) | |
| AR059957A1 (es) | DERIVADOS DE ESPIROINDOLINONA, MÉTODOS PARA SU PREPARACIoN, UNA COMPOSICIoN FARMACÉUTICA QUE LOS CONTIENE Y SU USO EN LA FABRICACIoN DE MEDICAMENTOS PARA EL TRATAMIENTO DEL CÁNCER. | |
| AR058587A1 (es) | Compuestos de pirrolo-1,5-naftiridinona,su uso como agentes antibacterianos, composiciones farmaceuticas que los contienen y compuestos intermediarios para preparar dichos compuestos | |
| AR043508A1 (es) | 1-amino 1-h-imidazoquinolinas y su uso como inmunomoduladores | |
| AR037736A1 (es) | Derivados de pirimidina como moduladores o inhibidores de la actividad del factor de crecimiento insulinico tipo 1 (igf-1r) | |
| AR057986A1 (es) | Compuesto heterociclico y su uso farmaceutico | |
| AR020165A1 (es) | Derivados de pirimidinas sustituidas, su procedimiento de preparacion, composiciones farmaceuticas que las contienen y el uso de los mismos para la preparacion de medicamentos | |
| ECSP11011561A (es) | Derivados aminobutíricos sustituidos como inhibidores de neprilisina | |
| AR046711A1 (es) | 5-7-diaminopirazolo[4,3d]pirimidinas como inhibidores de la pde-5,composiciones farmaceuticas que las contienen y usos en el tratamiento de hipertensiones | |
| AR069772A1 (es) | Derivados heterociclicos, una composicion farmaceutica y un juego que los comprenden y su uso en la preparacion de un medicamento para el tratamiento de una infeccion parasitaria. | |
| AR061739A1 (es) | Nuevos derivados naftalenicos, su procedimiento de preparacion y las composiciones farmaceuticas que los contienen | |
| AR041184A1 (es) | Derivados de benzopiranonas, inhibidores de las cinasas dependientes de ciclinas y su uso | |
| AR058287A1 (es) | Derivados de isoquinolina y composicion farmaceutica | |
| AR073498A1 (es) | Derivados de tieno [2-3-d] pirimidin | |
| AR048362A1 (es) | Derivados de tetrahidronaftiridina y proceso para la preparacion de los mismos | |
| AR053109A1 (es) | DERIVADOS DE PIPERIDINA Y PIPERAZINA, UN METODO PARA SU PREPARACION, COMPOSICIONES FARMACEUTICAS QUE LOS CONTIENEN Y SU USO EN LA ELABORACIoN DE MEDICAMENTOS PARA EL TRATAMIENTO DE ENFERMEDADES MEDIADAS POR EL RECEPTOR DE QUIMIOQUINA CCR2. | |
| ECSP045420A (es) | Derivados de benzoxazina como moduladores 5-ht6 y usos de los mismos | |
| AR066604A1 (es) | Derivados de arilamida pirimidona, medicamentos que los contienen y usos terapeuticos para prevenir y/o tratar enfermedades neurodegenerativas fundamentalmente. | |
| AR046170A1 (es) | Derivados de pirimidin-2-amina y su uso como antagonistas del receptor de adenosina a 2b | |
| NI200900147A (es) | Nuevos derivados tricíclicos su procedimiento de preparación y las composiciones farmacéuticas que los contienen. | |
| AR061185A1 (es) | Compuestos heterociclicos como inhibidores de hsp90. composiciones farmaceuticas. | |
| UY28356A1 (es) | Derivados de benzimidazol, composiciones que los contienen, preparaciones de los mismos y sus usos |