SG11202012858QA - Crystal form of compound for inhibiting the activity of cdk4/6 and use thereof - Google Patents

Crystal form of compound for inhibiting the activity of cdk4/6 and use thereof

Info

Publication number
SG11202012858QA
SG11202012858QA SG11202012858QA SG11202012858QA SG11202012858QA SG 11202012858Q A SG11202012858Q A SG 11202012858QA SG 11202012858Q A SG11202012858Q A SG 11202012858QA SG 11202012858Q A SG11202012858Q A SG 11202012858QA SG 11202012858Q A SG11202012858Q A SG 11202012858QA
Authority
SG
Singapore
Prior art keywords
cdk4
inhibiting
activity
compound
crystal form
Prior art date
Application number
SG11202012858QA
Inventor
Yiqian Wang
Chunhui Zhang
Jiabing Wang
Lieming Ding
Original Assignee
Betta Pharmaceuticals Co Ltd
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 Betta Pharmaceuticals Co Ltd filed Critical Betta Pharmaceuticals Co Ltd
Publication of SG11202012858QA publication Critical patent/SG11202012858QA/en

Links

Classifications

    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4375Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/235Saturated compounds containing more than one carboxyl group
    • C07C59/245Saturated compounds containing more than one carboxyl group containing hydroxy or O-metal groups
    • C07C59/255Tartaric acid
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs
SG11202012858QA 2018-06-21 2019-06-21 Crystal form of compound for inhibiting the activity of cdk4/6 and use thereof SG11202012858QA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN2018092194 2018-06-21
PCT/CN2019/092239 WO2019242719A1 (en) 2018-06-21 2019-06-21 Crystal form of compound for inhibiting the activity of cdk4/6 and use thereof

Publications (1)

Publication Number Publication Date
SG11202012858QA true SG11202012858QA (en) 2021-02-25

Family

ID=68983152

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11202012858QA SG11202012858QA (en) 2018-06-21 2019-06-21 Crystal form of compound for inhibiting the activity of cdk4/6 and use thereof

Country Status (15)

Country Link
US (1) US20210261546A1 (en)
EP (1) EP3812386A4 (en)
JP (1) JP7430656B2 (en)
KR (1) KR20210024004A (en)
CN (2) CN113861191B (en)
AU (1) AU2019290722B2 (en)
BR (1) BR112020026052A2 (en)
CA (1) CA3104365A1 (en)
EA (1) EA202190036A1 (en)
IL (1) IL279579B2 (en)
MX (1) MX2020013847A (en)
PH (1) PH12020552236A1 (en)
SG (1) SG11202012858QA (en)
TW (1) TWI786303B (en)
WO (1) WO2019242719A1 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117222411A (en) * 2021-03-24 2023-12-12 贝达药业股份有限公司 Pharmaceutical combination, kit comprising same and use thereof
WO2023131179A1 (en) * 2022-01-05 2023-07-13 贝达药业股份有限公司 Use of benzimidazole derivative or salt thereof in treatment of leukemia
CN115872923B (en) * 2022-12-29 2023-04-28 成都泰和伟业生物科技有限公司 Compound and preparation method thereof

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105294655B (en) * 2014-07-26 2019-03-15 广东东阳光药业有限公司 The compound and application thereof of CDK type small molecular inhibitor
CN104592251B (en) * 2015-01-23 2019-10-01 上海复星医药产业发展有限公司 4- (condensed hetero ring substituted-amino) -1H- pyrazole-3-formamide class compound and application thereof
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
EP3319962B1 (en) * 2015-07-08 2020-05-13 H. Hoffnabb-La Roche Ag Aryl sultam derivatives as rorc modulators
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
WO2017102796A1 (en) * 2015-12-16 2017-06-22 F. Hoffmann-La Roche Ag HETEROARYL AMIDE SULTAM DERIVATIVES AS RORc MODULATORS
TWI646094B (en) * 2016-06-01 2019-01-01 大陸商貝達藥業股份有限公司 Crystal form of inhibitory protein kinase active compound and application thereof
ES2917377T3 (en) * 2016-12-22 2022-07-08 Betta Pharmaceuticals Co Ltd Benzimidazole derivatives, preparation procedures and uses thereof
US11351170B2 (en) * 2017-08-15 2022-06-07 Beijing Xuanyi Pharmasciences Co., Ltd. Substituted pyrimidines as CDK4/6 inhibitors

Also Published As

Publication number Publication date
EA202190036A1 (en) 2021-03-24
IL279579B (en) 2022-10-01
CN113861191B (en) 2023-09-19
IL279579A (en) 2021-03-01
AU2019290722B2 (en) 2023-12-21
TWI786303B (en) 2022-12-11
CA3104365A1 (en) 2019-12-26
JP7430656B2 (en) 2024-02-13
TW202016114A (en) 2020-05-01
US20210261546A1 (en) 2021-08-26
JP2021529175A (en) 2021-10-28
CN112424202A (en) 2021-02-26
AU2019290722A1 (en) 2021-01-28
BR112020026052A2 (en) 2021-03-23
KR20210024004A (en) 2021-03-04
MX2020013847A (en) 2021-04-28
CN113861191A (en) 2021-12-31
PH12020552236A1 (en) 2021-06-28
EP3812386A1 (en) 2021-04-28
IL279579B2 (en) 2023-02-01
CN112424202B (en) 2021-09-17
EP3812386A4 (en) 2022-03-30
WO2019242719A1 (en) 2019-12-26

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