SG10202004716RA - 2-h-indazole derivatives as cyclin-dependent kinase (cdk) inhibitors and therapeutic uses thereof - Google Patents
2-h-indazole derivatives as cyclin-dependent kinase (cdk) inhibitors and therapeutic uses thereofInfo
- Publication number
- SG10202004716RA SG10202004716RA SG10202004716RA SG10202004716RA SG10202004716RA SG 10202004716R A SG10202004716R A SG 10202004716RA SG 10202004716R A SG10202004716R A SG 10202004716RA SG 10202004716R A SG10202004716R A SG 10202004716RA SG 10202004716R A SG10202004716R A SG 10202004716RA
- Authority
- SG
- Singapore
- Prior art keywords
- cdk
- cyclin
- inhibitors
- therapeutic uses
- dependent kinase
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/14—Heterocyclic 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201462028427P | 2014-07-24 | 2014-07-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
SG10202004716RA true SG10202004716RA (en) | 2020-06-29 |
Family
ID=55163817
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG11201700037QA SG11201700037QA (en) | 2014-07-24 | 2015-07-24 | 2-h-indazole derivatives as cyclin-dependent kinase (cdk) inhibitors and therapeutic uses thereof |
SG10202004716RA SG10202004716RA (en) | 2014-07-24 | 2015-07-24 | 2-h-indazole derivatives as cyclin-dependent kinase (cdk) inhibitors and therapeutic uses thereof |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG11201700037QA SG11201700037QA (en) | 2014-07-24 | 2015-07-24 | 2-h-indazole derivatives as cyclin-dependent kinase (cdk) inhibitors and therapeutic uses thereof |
Country Status (19)
Country | Link |
---|---|
US (2) | US9878994B2 (en) |
EP (1) | EP3191469B1 (en) |
JP (1) | JP6490215B2 (en) |
KR (1) | KR20170031241A (en) |
CN (2) | CN110117273B (en) |
AP (1) | AP2017009728A0 (en) |
AU (1) | AU2015292425B2 (en) |
BR (1) | BR112017001058A2 (en) |
CA (1) | CA2954298A1 (en) |
CO (1) | CO2017000912A2 (en) |
EA (1) | EA032693B1 (en) |
IL (1) | IL249895B (en) |
MX (1) | MX2017000806A (en) |
MY (1) | MY187555A (en) |
PH (1) | PH12017500146B1 (en) |
SG (2) | SG11201700037QA (en) |
TW (1) | TWI675028B (en) |
WO (1) | WO2016014904A1 (en) |
ZA (1) | ZA201700652B (en) |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110117273B (en) * | 2014-07-24 | 2022-02-01 | 贝达医药公司 | 2H-indazole derivatives as Cyclin Dependent Kinase (CDK) inhibitors and their medical use |
TWI696617B (en) | 2015-04-28 | 2020-06-21 | 大陸商上海復尚慧創醫藥研究有限公司 | Certain protein kinase inhibitor |
CN106608879A (en) | 2015-10-27 | 2017-05-03 | 甘李药业股份有限公司 | Protein kinase inhibitor and its preparation method and medical application |
CN108602799B (en) * | 2016-02-06 | 2021-08-03 | 上海复尚慧创医药研究有限公司 | Kinase inhibitor |
WO2017160568A1 (en) * | 2016-03-16 | 2017-09-21 | Eli Lilly And Company | Combination therapy comprising the cdk4/6 inhibitor necitumumab and the egfr inhibitor abemaciclib for use in treating cancer |
US11077110B2 (en) | 2016-03-18 | 2021-08-03 | Tufts Medical Center | Compositions and methods for treating and preventing metabolic disorders |
CN107286134B (en) * | 2016-04-11 | 2019-04-12 | 上海勋和医药科技有限公司 | 2,4- disubstituted pyrimidines derivatives are as CDK inhibitor and its application |
WO2018045993A1 (en) * | 2016-09-09 | 2018-03-15 | 正大天晴药业集团股份有限公司 | Crystal form, salt type of substituted 2-hydro-pyrazole derivative and preparation method therefor |
ES2917377T3 (en) | 2016-12-22 | 2022-07-08 | Betta Pharmaceuticals Co Ltd | Benzimidazole derivatives, preparation procedures and uses thereof |
WO2018141296A1 (en) * | 2017-02-06 | 2018-08-09 | Betta Pharmaceuticals Co., Ltd | Protein tyrosine kinase modulators salt, crystallographic forms, and uses thereof |
CN108794452B (en) | 2017-05-05 | 2021-05-28 | 上海时莱生物技术有限公司 | Compound with kinase inhibition activity, preparation method and application thereof |
TW201920141A (en) * | 2017-08-15 | 2019-06-01 | 中國大陸商北京軒義醫藥科技有限公司 | CDK4/6 inhibitors and use thereof |
CN109503573A (en) * | 2017-09-14 | 2019-03-22 | 昆明圣加南生物科技有限公司 | 2- substituted anilinic pyrimidine derivatives and application thereof |
MX2020007959A (en) * | 2018-01-29 | 2020-09-18 | Beta Pharma Inc | 2h-indazole derivatives as cdk4 and cdk6 inhibitors and therapeutic uses thereof. |
JP2021521282A (en) | 2018-04-24 | 2021-08-26 | 上海海雁医薬科技有限公司Shanghai Haiyan Pharmaceutical Technology Co., Ltd. | CDK4 / 6 inhibitors, their pharmaceutically acceptable salts and crystalline polymorphs, and their applications |
RU2762557C1 (en) | 2018-04-26 | 2021-12-21 | Пфайзер Инк. | Derivatives of 2-aminopyridine or 2-aminopyrimidine as cyclin-dependent kinase inhibitors |
SG11202012312UA (en) * | 2018-06-18 | 2021-01-28 | UCB Biopharma SRL | Gremlin-1 antagonist for the prevention and treatment of cancer |
EP3849537A4 (en) | 2018-09-10 | 2022-06-29 | Mirati Therapeutics, Inc. | Combination therapies |
JP2022519205A (en) * | 2019-01-29 | 2022-03-22 | ベータ・ファーマ・インコーポレイテッド | 2H-indazole derivative as a therapeutic agent for brain tumors and brain metastases |
SG11202109463PA (en) * | 2019-03-20 | 2021-10-28 | Beta Pharma Inc | Crystalline and amorphous forms of n-(5-((4-ethylpiperazin-1-yl)methyl)pyridine-2-yl)-5-fluoro-4-(3-isopropyl-2-methyl-2h-indazol-5-yl)pyrimidin-2-amine and its salts, and preparation methods and therapeutic uses thereof |
WO2020224568A1 (en) * | 2019-05-05 | 2020-11-12 | Qilu Regor Therapeutics Inc. | Cdk inhibitors |
WO2021061695A1 (en) * | 2019-09-23 | 2021-04-01 | Beta Pharma, Inc. | Treatment of egfr mutant-related cancers using a combination of egfr and cdk4/6 inhibitors |
CN111100117B (en) * | 2019-12-18 | 2021-02-19 | 上海倍而达药业有限公司 | Crystal form A of aminopyrimidine compound mesylate and preparation method and application thereof |
CN113880816A (en) * | 2020-07-01 | 2022-01-04 | 杭州百诚医药科技股份有限公司 | Piperazine-containing aminopyrimidine derivative and application thereof |
CN114539225B (en) * | 2020-11-11 | 2024-02-20 | 上海拓界生物医药科技有限公司 | 2-amino-pyrimidines |
TW202237585A (en) | 2020-11-27 | 2022-10-01 | 瑞士商瑞森製藥公司 | Cdk inhibitors |
WO2022149057A1 (en) | 2021-01-05 | 2022-07-14 | Rhizen Pharmaceuticals Ag | Cdk inhibitors |
WO2022162122A1 (en) | 2021-01-29 | 2022-08-04 | Biotx.Ai Gmbh | Genetically verified netosis inhibitor for use in the treatment of a sars-cov2 infection |
CN115703760A (en) * | 2021-08-11 | 2023-02-17 | 山东大学 | 2,4-disubstituted pyrimidines cyclin dependent kinase inhibitor and preparation method and application thereof |
CN115650968B (en) * | 2022-12-27 | 2023-03-21 | 英矽智能科技(上海)有限公司 | Novel pyridazinone compounds as CDK selective inhibitors |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
YU54202A (en) | 2000-01-18 | 2006-01-16 | Agouron Pharmaceuticals Inc. | Indazole compounds,pharmaceutical compositions,and methods for mediating or inhibiting cell proliferation |
GEP20063909B (en) | 2002-01-22 | 2006-08-25 | Warner Lambert Co | 2-(PYRIDIN-2-YLAMINO)-PYRIDO[2,3d] PYRIMIDIN-7-ONES |
ES2309368T3 (en) | 2002-12-02 | 2008-12-16 | F. Hoffmann-La Roche Ag | DERIVATIVES OF INDAZOL AS AN ANTAGONIST OF CRF. |
WO2006008874A1 (en) * | 2004-05-21 | 2006-01-26 | Banyu Pharmaceutical Co., Ltd. | SELECTIVE INHIBITORS AGAINST Cdk4 AND Cdk6 HAVING AMINOTHIAZOLE SKELETON |
WO2007124288A1 (en) * | 2006-04-19 | 2007-11-01 | Novartis Ag | Indazole compounds and methods for inhibition of cdc7 |
JO3235B1 (en) * | 2006-05-26 | 2018-03-08 | Astex Therapeutics Ltd | Pyrrolopyrimidine compounds and their uses |
US9259399B2 (en) * | 2007-11-07 | 2016-02-16 | Cornell University | Targeting CDK4 and CDK6 in cancer therapy |
CA2986640C (en) * | 2008-06-27 | 2019-03-26 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
WO2010034649A1 (en) * | 2008-09-25 | 2010-04-01 | F. Hoffmann-La Roche Ag | 2,3-substituted indazole or 4,5,6,7-tetrahydro-indazoles as fxr modulators against dyslipidemia and related diseases |
PA8852901A1 (en) * | 2008-12-22 | 2010-07-27 | Lilly Co Eli | PROTEIN CINASE INHIBITORS |
CN110117273B (en) * | 2014-07-24 | 2022-02-01 | 贝达医药公司 | 2H-indazole derivatives as Cyclin Dependent Kinase (CDK) inhibitors and their medical use |
-
2015
- 2015-07-24 CN CN201910409416.1A patent/CN110117273B/en active Active
- 2015-07-24 EP EP15823933.5A patent/EP3191469B1/en active Active
- 2015-07-24 MX MX2017000806A patent/MX2017000806A/en unknown
- 2015-07-24 AP AP2017009728A patent/AP2017009728A0/en unknown
- 2015-07-24 EA EA201790122A patent/EA032693B1/en unknown
- 2015-07-24 CN CN201580047916.5A patent/CN106687454B8/en active Active
- 2015-07-24 WO PCT/US2015/041915 patent/WO2016014904A1/en active Application Filing
- 2015-07-24 KR KR1020177004776A patent/KR20170031241A/en not_active Application Discontinuation
- 2015-07-24 AU AU2015292425A patent/AU2015292425B2/en active Active
- 2015-07-24 BR BR112017001058-5A patent/BR112017001058A2/en not_active Application Discontinuation
- 2015-07-24 US US15/328,813 patent/US9878994B2/en active Active
- 2015-07-24 SG SG11201700037QA patent/SG11201700037QA/en unknown
- 2015-07-24 SG SG10202004716RA patent/SG10202004716RA/en unknown
- 2015-07-24 MY MYPI2017700116A patent/MY187555A/en unknown
- 2015-07-24 TW TW104124158A patent/TWI675028B/en not_active IP Right Cessation
- 2015-07-24 JP JP2017525318A patent/JP6490215B2/en active Active
- 2015-07-24 CA CA2954298A patent/CA2954298A1/en not_active Abandoned
-
2017
- 2017-01-02 IL IL249895A patent/IL249895B/en active IP Right Grant
- 2017-01-24 PH PH12017500146A patent/PH12017500146B1/en unknown
- 2017-01-26 ZA ZA2017/00652A patent/ZA201700652B/en unknown
- 2017-01-31 CO CONC2017/0000912A patent/CO2017000912A2/en unknown
-
2018
- 2018-01-29 US US15/882,620 patent/US10239864B2/en active Active
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