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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
SG11202000418XA (en) 2017-07-18 2020-02-27 Nuvation Bio Inc Heterocyclic compounds as adenosine antagonists
EP3654982A4 (en) 2017-07-18 2021-04-14 Nuvation Bio Inc. 1,8-NAPHTHYRIDINONE COMPOUNDS AND THEIR USES
WO2019161224A1 (en) 2018-02-15 2019-08-22 GiraFpharma LLC Heterocyclic compounds as kinase inhibitors
SG11202012312UA (en) * 2018-06-18 2021-01-28 UCB Biopharma SRL Gremlin-1 antagonist for the prevention and treatment of cancer
CN113924095A (zh) 2019-01-18 2022-01-11 诺维逊生物股份有限公司 作为腺苷拮抗剂的杂环化合物
WO2020150676A1 (en) 2019-01-18 2020-07-23 Nuvation Bio Inc. 1,8-naphthyridinone compounds and uses thereof
EP3917532A4 (en) * 2019-01-29 2022-09-28 Beta Pharma, Inc. 2h-indazole derivatives as therapeutic agents for brain cancers and brain metastases
SG11202112229UA (en) 2019-05-05 2021-12-30 Qilu Regor Therapeutics Inc Cdk inhibitors
CN115768763B (zh) * 2020-06-22 2025-09-09 正大天晴药业集团股份有限公司 一种cdk4/6抑制剂的制备方法
US20230416271A1 (en) * 2020-11-26 2023-12-28 Chengdu Cynogen Bio-Pharmaceutical Technology Co., Ltd. Heteroarylquinazoline compounds as protein kinase inhibitors
TW202237585A (zh) 2020-11-27 2022-10-01 瑞士商瑞森製藥公司 Cdk抑制劑
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
PL220952B1 (pl) 2002-01-22 2016-01-29 Warner Lambert Co 2-(Pirydyn-2-yloamino)pirydo[2,3-d]pirymidyn-7-ony
ATE412650T1 (de) * 2003-07-11 2008-11-15 Warner Lambert Co Isethionat salz eines selektiven cdk4 inhibitors
JPWO2006008874A1 (ja) * 2004-05-21 2008-05-01 萬有製薬株式会社 アミノチアゾ−ル骨格を有するCdk4、6選択的阻害剤
JO3235B1 (ar) 2006-05-26 2018-03-08 Astex Therapeutics Ltd مركبات بيررولوبيريميدين و استعمالاتها
US9259399B2 (en) * 2007-11-07 2016-02-16 Cornell University Targeting CDK4 and CDK6 in cancer therapy
PE20110419A1 (es) * 2008-08-22 2011-07-13 Novartis Ag Compuestos de pirrolo-pirimidina como inhibidores de cdk
PA8852901A1 (es) 2008-12-22 2010-07-27 Lilly Co Eli Inhibidores de proteina cinasa
ES2687477T3 (es) * 2013-12-31 2018-10-25 Xuanzhu Pharma Co., Ltd. Inhibidor de quinasa y su uso
TWI675028B (zh) 2014-07-24 2019-10-21 美商貝達醫藥公司 做為週期素依賴型激酶(cdk)抑制劑之2-h-吲唑衍生物及其醫療用途
JP6726677B2 (ja) * 2015-03-11 2020-07-22 チア タイ ティエンチン ファーマシューティカル グループ カンパニー リミテッドChia Tai Tianqing Pharmaceutical Group Co., Ltd. 抗がん剤としての置換2−h−ピラゾール誘導体
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
KR20200115583A (ko) 2020-10-07
US11352341B2 (en) 2022-06-07
JP2021512161A (ja) 2021-05-13
TW201940166A (zh) 2019-10-16
AU2019211491A1 (en) 2020-07-30
EP3746072A4 (en) 2021-06-02
WO2019148161A1 (en) 2019-08-01
JP7337395B2 (ja) 2023-09-04
PH12020551155A1 (en) 2021-06-07
AU2019211491B2 (en) 2024-03-14
CA3088381A1 (en) 2019-08-01
SG11202006748RA (en) 2020-08-28
BR112020015405A2 (pt) 2020-12-08
EP3746072B1 (en) 2023-04-12
EA202091450A1 (ru) 2021-01-14
CN111989099A (zh) 2020-11-24
US20210139459A1 (en) 2021-05-13
EP3746072A1 (en) 2020-12-09
IL275948A (en) 2020-08-31

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