MX2020007959A - Derivados de 2h-indazol e inhibidores de cdk4 y cdk6 y sus usos terapeuticos. - Google Patents

Derivados de 2h-indazol e inhibidores de cdk4 y cdk6 y sus usos terapeuticos.

Info

Publication number
MX2020007959A
MX2020007959A MX2020007959A MX2020007959A MX2020007959A MX 2020007959 A MX2020007959 A MX 2020007959A MX 2020007959 A MX2020007959 A MX 2020007959A MX 2020007959 A MX2020007959 A MX 2020007959A MX 2020007959 A MX2020007959 A MX 2020007959A
Authority
MX
Mexico
Prior art keywords
sup
therapeutic uses
cdk4
cyclin
prodrugs
Prior art date
Application number
MX2020007959A
Other languages
English (en)
Inventor
Michael Nicholas Greco
Jirong Peng
Don Zhang
Michael John Costanzo
Original Assignee
Beta Pharma Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Beta Pharma Inc filed Critical Beta Pharma Inc
Publication of MX2020007959A publication Critical patent/MX2020007959A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

Se divulgan compuestos 2H-indazol 2-aminopirimidina sustituidos de la fórmula (I), (ver Fórmula) donde R1 es hidrogeno y su profármaco, donde R1 es un grupo metabolizable en condiciones fisiológicas, como inhibidores de cinasa dependiente de ciclina (CDK) y de la proliferación celular y los usos terapéuticos y métodos de preparación de ellos. Estos compuestos y las sales farmacéuticamente aceptables, solvatos, profármacos y composiciones farmacéuticas de ellos, son útiles para el tratamiento de enfermedades y trastornos asociados con la actividad de las cinasas dependientes de ciclina, en particular CDK4/6, que incluyen en forma no taxativa diversos canceres y enfermedades o afecciones con la inflación.
MX2020007959A 2018-01-29 2019-01-29 Derivados de 2h-indazol e inhibidores de cdk4 y cdk6 y sus usos terapeuticos. MX2020007959A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201862623516P 2018-01-29 2018-01-29
PCT/US2019/015547 WO2019148161A1 (en) 2018-01-29 2019-01-29 2h-indazole derivatives as cdk4 and cdk6 inhibitors and therapeutic uses thereof

Publications (1)

Publication Number Publication Date
MX2020007959A true MX2020007959A (es) 2020-09-18

Family

ID=67394794

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2020007959A MX2020007959A (es) 2018-01-29 2019-01-29 Derivados de 2h-indazol e inhibidores de cdk4 y cdk6 y sus usos terapeuticos.

Country Status (15)

Country Link
US (1) US11352341B2 (es)
EP (1) EP3746072B1 (es)
JP (1) JP7337395B2 (es)
KR (1) KR20200115583A (es)
CN (1) CN111989099A (es)
AU (1) AU2019211491B2 (es)
BR (1) BR112020015405A2 (es)
CA (1) CA3088381A1 (es)
EA (1) EA202091450A1 (es)
IL (1) IL275948A (es)
MX (1) MX2020007959A (es)
PH (1) PH12020551155A1 (es)
SG (1) SG11202006748RA (es)
TW (1) TW201940166A (es)
WO (1) WO2019148161A1 (es)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111163780A (zh) 2017-07-18 2020-05-15 诺维逊生物股份有限公司 作为腺苷拮抗剂的杂环化合物
CA3070073A1 (en) 2017-07-18 2019-01-24 Nuvation Bio Inc. 1,8-naphthyridinone compounds and uses thereof
JP2021514359A (ja) 2018-02-15 2021-06-10 ニューベイション・バイオ・インコーポレイテッドNuvation Bio Inc. キナーゼ阻害剤としての複素環式化合物
MX2020013808A (es) * 2018-06-18 2021-05-27 UCB Biopharma SRL Antagonista de gremlina-1 para la prevencion y el tratamiento del cancer.
AU2020208644A1 (en) 2019-01-18 2021-08-26 Nuvation Bio Inc. Heterocyclic compounds as adenosine antagonists
WO2020150676A1 (en) 2019-01-18 2020-07-23 Nuvation Bio Inc. 1,8-naphthyridinone compounds and uses thereof
US20220079944A1 (en) * 2019-01-29 2022-03-17 Beta Pharma, Inc. 2h-indazole derivatives as therapeutic agents for brain cancers and brain metastases
MA55909A (fr) * 2019-05-05 2022-03-16 Qilu Regor Therapeutics Inc Inhibiteurs de cdk
US12570633B2 (en) 2020-06-22 2026-03-10 Chia Tai Tianqing Pharmaceutical Group Co., Ltd Preparation method for CDK4/6 inhibitor
US20230416271A1 (en) * 2020-11-26 2023-12-28 Chengdu Cynogen Bio-Pharmaceutical Technology Co., Ltd. Heteroarylquinazoline compounds as protein kinase inhibitors
WO2022113003A1 (en) 2020-11-27 2022-06-02 Rhizen Pharmaceuticals Ag Cdk inhibitors
WO2022149057A1 (en) 2021-01-05 2022-07-14 Rhizen Pharmaceuticals Ag Cdk inhibitors

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MXPA04005939A (es) 2002-01-22 2005-01-25 Warner Lambert Co 2-(piridin-2-ilamino)-pirido[2,3-d]pirimidin-7-onas.
AU2004255934B2 (en) 2003-07-11 2010-02-25 Warner-Lambert Company Llc Isethionate salt of a selective CDK4 inhibitor
CN1956982A (zh) * 2004-05-21 2007-05-02 万有制药株式会社 具有氨基噻唑骨架的Cdk4、6选择性抑制剂
TWI398252B (zh) 2006-05-26 2013-06-11 諾華公司 吡咯并嘧啶化合物及其用途
WO2009061345A2 (en) 2007-11-07 2009-05-14 Cornell Research Foundation, Inc. Targeting cdk4 and cdk6 in cancer therapy
ES2522346T3 (es) * 2008-08-22 2014-11-14 Novartis Ag Compuestos de pirrolopirimidina como inhibidores de CDK
PA8852901A1 (es) 2008-12-22 2010-07-27 Lilly Co Eli Inhibidores de proteina cinasa
US9796701B2 (en) * 2013-12-31 2017-10-24 Xuanzhu Pharma Co., Ltd. Kinase inhibitor and use thereof
CA2954298A1 (en) * 2014-07-24 2016-01-28 Beta Pharma, Inc. 2-h-indazole derivatives as cyclin-dependent kinase (cdk) inhibitors and therapeutic uses thereof
CN111333627B (zh) * 2015-03-11 2024-09-13 正大天晴药业集团股份有限公司 作为抗癌药物的取代的2-氢-吡唑衍生物
CN107286134B (zh) * 2016-04-11 2019-04-12 上海勋和医药科技有限公司 2,4-二取代嘧啶衍生物作为cdk抑制剂及其应用

Also Published As

Publication number Publication date
AU2019211491B2 (en) 2024-03-14
SG11202006748RA (en) 2020-08-28
US20210139459A1 (en) 2021-05-13
WO2019148161A1 (en) 2019-08-01
IL275948A (en) 2020-08-31
JP7337395B2 (ja) 2023-09-04
CA3088381A1 (en) 2019-08-01
JP2021512161A (ja) 2021-05-13
PH12020551155A1 (en) 2021-06-07
US11352341B2 (en) 2022-06-07
KR20200115583A (ko) 2020-10-07
TW201940166A (zh) 2019-10-16
AU2019211491A1 (en) 2020-07-30
EP3746072B1 (en) 2023-04-12
EP3746072A4 (en) 2021-06-02
CN111989099A (zh) 2020-11-24
BR112020015405A2 (pt) 2020-12-08
EP3746072A1 (en) 2020-12-09
EA202091450A1 (ru) 2021-01-14

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