CN107922425B - 制备parp抑制剂、结晶形式的方法及其用途 - Google Patents
制备parp抑制剂、结晶形式的方法及其用途 Download PDFInfo
- Publication number
- CN107922425B CN107922425B CN201680048637.5A CN201680048637A CN107922425B CN 107922425 B CN107922425 B CN 107922425B CN 201680048637 A CN201680048637 A CN 201680048637A CN 107922425 B CN107922425 B CN 107922425B
- Authority
- CN
- China
- Prior art keywords
- compound
- crystalline form
- cancer
- degrees
- def
- 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.)
- Active
Links
Images
Classifications
-
- 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
- C07D471/22—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 systems contains four 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
- A61K31/435—Heterocyclic 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
- A61K31/4353—Heterocyclic 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
-
- 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
- A61K31/435—Heterocyclic 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
- A61K31/4353—Heterocyclic 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
- A61K31/437—Heterocyclic 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 five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
- A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
- A61K31/5517—1,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
-
- 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
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
- C07D471/04—Ortho-condensed systems
-
- 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
- C07D471/12—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 three hetero rings
- C07D471/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Saccharide Compounds (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202011223061.6A CN112521390A (zh) | 2015-08-25 | 2016-08-22 | 制备parp抑制剂、结晶形式的方法及其用途 |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2015088003 | 2015-08-25 | ||
| CNPCT/CN2015/088003 | 2015-08-25 | ||
| PCT/CN2016/096200 WO2017032289A1 (en) | 2015-08-25 | 2016-08-22 | Process for preparing parp inhibitor, crystalline forms, and uses thereof |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202011223061.6A Division CN112521390A (zh) | 2015-08-25 | 2016-08-22 | 制备parp抑制剂、结晶形式的方法及其用途 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN107922425A CN107922425A (zh) | 2018-04-17 |
| CN107922425B true CN107922425B (zh) | 2021-06-01 |
Family
ID=58099633
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201680048637.5A Active CN107922425B (zh) | 2015-08-25 | 2016-08-22 | 制备parp抑制剂、结晶形式的方法及其用途 |
| CN202011223061.6A Pending CN112521390A (zh) | 2015-08-25 | 2016-08-22 | 制备parp抑制剂、结晶形式的方法及其用途 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202011223061.6A Pending CN112521390A (zh) | 2015-08-25 | 2016-08-22 | 制备parp抑制剂、结晶形式的方法及其用途 |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US10457680B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP3341375B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP6940039B2 (cg-RX-API-DMAC7.html) |
| KR (1) | KR20180041748A (cg-RX-API-DMAC7.html) |
| CN (2) | CN107922425B (cg-RX-API-DMAC7.html) |
| AU (1) | AU2016312011B2 (cg-RX-API-DMAC7.html) |
| BR (1) | BR112018003634B1 (cg-RX-API-DMAC7.html) |
| CA (1) | CA2994895A1 (cg-RX-API-DMAC7.html) |
| EA (1) | EA037366B1 (cg-RX-API-DMAC7.html) |
| IL (2) | IL257442B2 (cg-RX-API-DMAC7.html) |
| MX (1) | MX385450B (cg-RX-API-DMAC7.html) |
| NZ (1) | NZ739876A (cg-RX-API-DMAC7.html) |
| TW (1) | TWI736550B (cg-RX-API-DMAC7.html) |
| WO (1) | WO2017032289A1 (cg-RX-API-DMAC7.html) |
| ZA (1) | ZA201800765B (cg-RX-API-DMAC7.html) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NO2797921T3 (cg-RX-API-DMAC7.html) | 2011-12-31 | 2018-02-03 | ||
| EA037366B1 (ru) | 2015-08-25 | 2021-03-18 | Бейджин, Лтд. | Способ получения ингибитора parp, кристаллические формы и их применения |
| US11202782B2 (en) | 2016-09-27 | 2021-12-21 | Beigene, Ltd. | Treatment cancers using a combination comprising PARP inhibitors |
| CN110392687B (zh) * | 2017-02-28 | 2022-08-02 | 百济神州(苏州)生物科技有限公司 | 稠合的四环或五环二氢二氮杂䓬并咔唑酮的盐的结晶形式及其用途 |
| US12121518B2 (en) | 2017-03-09 | 2024-10-22 | The Board Of Supervisors Of Louisiana State Universi And Agricultural And Mechanical College | PARP-1 and methods of use thereof |
| WO2018165615A1 (en) | 2017-03-09 | 2018-09-13 | The Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College | Parp-1 and methods of use thereof |
| EP3654985A4 (en) * | 2017-07-17 | 2021-04-07 | BeiGene, Ltd. | TREATMENT OF CANCERS USING A COMBINATION INCLUDING PARP INHIBITORS, TEMOZOLOMIDE AND / OR RADIATION THERAPY |
| CA3097312A1 (en) * | 2018-05-18 | 2019-11-21 | Novartis Ag | Crystalline forms of a tlr7/tlr8 inhibitor |
| TW202002985A (zh) * | 2018-06-01 | 2020-01-16 | 英屬開曼群島商百濟神州有限公司 | 在胃癌治療中的parp抑制劑維持療法 |
| USD926356S1 (en) * | 2019-03-14 | 2021-07-27 | Tuanfang Liu | Battery for electronic cigarette |
| CN113004279B (zh) * | 2019-05-10 | 2023-01-06 | 百济神州(苏州)生物科技有限公司 | 一种控制含parp抑制剂倍半水合物产物的含水量的方法 |
| CN111171001B (zh) * | 2019-05-16 | 2022-04-29 | 百济神州(苏州)生物科技有限公司 | 一种parp抑制剂中间体的结晶方法 |
| CN111171002B (zh) * | 2019-05-16 | 2021-04-06 | 百济神州(苏州)生物科技有限公司 | 一种parp抑制剂中间体的制备方法 |
| MX2021014339A (es) * | 2019-05-31 | 2022-01-06 | Beigene Ltd | Preparacion de granulo inhibidor de parp y proceso de preparacion del mismo. |
| CN112007011B (zh) * | 2019-05-31 | 2024-07-23 | 百济神州(苏州)生物科技有限公司 | 一种parp抑制剂微丸胶囊及其制备工艺 |
| WO2021046014A1 (en) | 2019-09-03 | 2021-03-11 | Teva Czech Industries S.R.O | Solid state forms of pamiparib and process for preparation thereof |
| AU2024265078A1 (en) | 2023-05-04 | 2025-12-11 | Revolution Medicines, Inc. | Combination therapy for a ras related disease or disorder |
| US20250049810A1 (en) | 2023-08-07 | 2025-02-13 | Revolution Medicines, Inc. | Methods of treating a ras protein-related disease or disorder |
| US20250154171A1 (en) | 2023-10-12 | 2025-05-15 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2025171296A1 (en) | 2024-02-09 | 2025-08-14 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2025217307A1 (en) | 2024-04-09 | 2025-10-16 | Revolution Medicines, Inc. | Methods for predicting response to a ras(on) inhibitor and combination therapies |
| WO2025240847A1 (en) | 2024-05-17 | 2025-11-20 | Revolution Medicines, Inc. | Ras inhibitors |
| WO2025255438A1 (en) | 2024-06-07 | 2025-12-11 | Revolution Medicines, Inc. | Methods of treating a ras protein-related disease or disorder |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002044183A2 (en) * | 2000-12-01 | 2002-06-06 | Guilford Pharmaceuticals Inc. | Benzoazepine and benzodiazepine derivatives and their use as parp inhibitors |
| WO2004063198A1 (en) * | 2003-01-09 | 2004-07-29 | Pfizer Inc. | Diazepinoindole derivatives as kinase inhibitors |
| CN103703004A (zh) * | 2011-12-31 | 2014-04-02 | 百济神州有限公司 | 作为parp抑制剂的稠合的四环或五环的二氢二氮杂*并咔唑酮 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SI20691B (sl) | 1999-01-11 | 2008-10-31 | Agouron Pharma | Triciklični inhibitorji poli(ADP-riboza) polimeraz |
| LT2767537T (lt) | 2008-08-06 | 2017-08-10 | Medivation Technologies, Inc. | Poli(adp-ribozės)polimerazės (parp) dihidropiridoftalazinono inhibitoriai |
| HUE060420T2 (hu) | 2013-09-13 | 2023-02-28 | Beigene Switzerland Gmbh | Anti-PD1 antitestek, valamint terapeutikumként és diagnosztikumként történõ alkalmazásuk |
| KR102003754B1 (ko) | 2014-07-03 | 2019-07-25 | 베이진 엘티디 | Pd-l1 항체와 이를 이용한 치료 및 진단 |
| US9637488B2 (en) | 2015-01-29 | 2017-05-02 | Fuqiang Ruan | Heterocyclic compounds as inhibitors of class I PI3KS |
| EA037366B1 (ru) | 2015-08-25 | 2021-03-18 | Бейджин, Лтд. | Способ получения ингибитора parp, кристаллические формы и их применения |
| US11202782B2 (en) * | 2016-09-27 | 2021-12-21 | Beigene, Ltd. | Treatment cancers using a combination comprising PARP inhibitors |
| CN110392687B (zh) * | 2017-02-28 | 2022-08-02 | 百济神州(苏州)生物科技有限公司 | 稠合的四环或五环二氢二氮杂䓬并咔唑酮的盐的结晶形式及其用途 |
| EP3654985A4 (en) * | 2017-07-17 | 2021-04-07 | BeiGene, Ltd. | TREATMENT OF CANCERS USING A COMBINATION INCLUDING PARP INHIBITORS, TEMOZOLOMIDE AND / OR RADIATION THERAPY |
| CN113004279B (zh) * | 2019-05-10 | 2023-01-06 | 百济神州(苏州)生物科技有限公司 | 一种控制含parp抑制剂倍半水合物产物的含水量的方法 |
-
2016
- 2016-08-22 EA EA201890547A patent/EA037366B1/ru not_active IP Right Cessation
- 2016-08-22 EP EP16838548.2A patent/EP3341375B1/en not_active Not-in-force
- 2016-08-22 KR KR1020187008548A patent/KR20180041748A/ko not_active Ceased
- 2016-08-22 IL IL257442A patent/IL257442B2/en unknown
- 2016-08-22 NZ NZ739876A patent/NZ739876A/en not_active IP Right Cessation
- 2016-08-22 CN CN201680048637.5A patent/CN107922425B/zh active Active
- 2016-08-22 WO PCT/CN2016/096200 patent/WO2017032289A1/en not_active Ceased
- 2016-08-22 MX MX2018002322A patent/MX385450B/es unknown
- 2016-08-22 CN CN202011223061.6A patent/CN112521390A/zh active Pending
- 2016-08-22 CA CA2994895A patent/CA2994895A1/en active Pending
- 2016-08-22 AU AU2016312011A patent/AU2016312011B2/en not_active Ceased
- 2016-08-22 JP JP2018510352A patent/JP6940039B2/ja not_active Expired - Fee Related
- 2016-08-22 US US15/753,993 patent/US10457680B2/en active Active
- 2016-08-22 IL IL296835A patent/IL296835A/en unknown
- 2016-08-22 BR BR112018003634-0A patent/BR112018003634B1/pt not_active IP Right Cessation
- 2016-08-24 TW TW105127160A patent/TWI736550B/zh not_active IP Right Cessation
-
2018
- 2018-02-06 ZA ZA201800765A patent/ZA201800765B/en unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002044183A2 (en) * | 2000-12-01 | 2002-06-06 | Guilford Pharmaceuticals Inc. | Benzoazepine and benzodiazepine derivatives and their use as parp inhibitors |
| WO2004063198A1 (en) * | 2003-01-09 | 2004-07-29 | Pfizer Inc. | Diazepinoindole derivatives as kinase inhibitors |
| CN103703004A (zh) * | 2011-12-31 | 2014-04-02 | 百济神州有限公司 | 作为parp抑制剂的稠合的四环或五环的二氢二氮杂*并咔唑酮 |
Non-Patent Citations (4)
| Title |
|---|
| Crystalline Polymorphism of Organic Compounds;Mino R. Caira;《Topics in current chemistry》;19980101;第198卷;全文 * |
| First-principles and direct design approaches for the control of pharmaceutical crystallization;Mitsuko Fujiwara等;《Journal of Process Control》;20050801;第15卷(第5期);全文 * |
| From Form to Function: Crystallization of Active Pharmaceutical Ingredients;Narayan Variankaval等;《AIChE》;20080603;第54卷(第7期);晶型章节 * |
| High-throughput crystallization: polymorphs, salts, co-crystals and solvates of pharmaceutical solids;Sherry L. Morissette等;《Advanced Drug Delivery Reviews》;20040223;第54卷(第7期);全文 * |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2017032289A1 (en) | 2017-03-02 |
| JP6940039B2 (ja) | 2021-09-22 |
| IL257442A (en) | 2018-04-30 |
| EP3341375B1 (en) | 2022-04-13 |
| BR112018003634B1 (pt) | 2023-11-21 |
| CA2994895A1 (en) | 2017-03-02 |
| IL257442B2 (en) | 2023-03-01 |
| CN107922425A (zh) | 2018-04-17 |
| US20190177325A1 (en) | 2019-06-13 |
| KR20180041748A (ko) | 2018-04-24 |
| TW201718586A (zh) | 2017-06-01 |
| BR112018003634A8 (pt) | 2023-01-17 |
| AU2016312011A1 (en) | 2018-03-08 |
| US10457680B2 (en) | 2019-10-29 |
| MX2018002322A (es) | 2018-04-11 |
| CN112521390A (zh) | 2021-03-19 |
| MX385450B (es) | 2025-03-18 |
| ZA201800765B (en) | 2019-10-30 |
| BR112018003634A2 (en) | 2018-11-21 |
| JP2018528199A (ja) | 2018-09-27 |
| EA037366B1 (ru) | 2021-03-18 |
| AU2016312011B2 (en) | 2021-02-04 |
| EP3341375A4 (en) | 2019-01-16 |
| EP3341375A1 (en) | 2018-07-04 |
| IL296835A (en) | 2022-11-01 |
| IL257442B (en) | 2022-11-01 |
| EA201890547A1 (ru) | 2018-07-31 |
| NZ739876A (en) | 2022-09-30 |
| TWI736550B (zh) | 2021-08-21 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN107922425B (zh) | 制备parp抑制剂、结晶形式的方法及其用途 | |
| EP2850082B1 (en) | 1-(3,3-dimethylbutyl)-3-(2-fluoro-4-methyl-5-(7-methyl-2-(methylamino)pyrido(2,3-d)pyrimidin-6-yl)phenyl)urea as Raf kinase inhibitor for the treatment of cancer | |
| WO2021190467A1 (zh) | 含螺环的喹唑啉化合物 | |
| WO2021129820A1 (zh) | 含螺环的喹唑啉化合物 | |
| WO2022017533A1 (zh) | 用作cdk7激酶抑制剂的化合物及其应用 | |
| CN113454081A (zh) | 咪唑并吡啶基化合物及其用于治疗增生性疾病的用途 | |
| JP2019526605A (ja) | 置換2−h−ピラゾール誘導体の結晶形、塩型及びその製造方法 | |
| CN115433187A (zh) | 稠合的四环或五环二氢二氮杂䓬并咔唑酮的盐的结晶形式组合物及其用途 | |
| CN107879975A (zh) | 组蛋白去乙酰化酶抑制剂及其应用 | |
| HK40040143A (en) | Process for preparing parp inhibitor, crystalline forms, and uses thereof | |
| EP4596553A1 (en) | Salt of dioxane quinoline compound, crystal form thereof, preparation methods therefor and uses thereof | |
| CN103373971A (zh) | 作为蛋白激酶抑制剂的脲类化合物 | |
| TW202519531A (zh) | 含丙烯酮類生物抑制劑的晶型及其製備方法和應用 | |
| HK40061853B (zh) | 用作cdk7激酶抑制剂的化合物及其应用 | |
| WO2025231053A1 (en) | Solid forms of 6-chloro-3-[(1r)-1-[3,6-dimethyl-2-(2-methylindazol-5-yl)-4-oxo-chromen-8-yl]ethoxy]pyridine-2-carboxamide | |
| WO2024008083A1 (zh) | 用作cdk7激酶抑制剂的化合物及其应用 | |
| WO2025242167A1 (zh) | Pkmyt1抑制剂的多晶型、其制备方法及其应用 | |
| WO2021092892A1 (zh) | 喹啉或喹唑啉类化合物在制备抗肿瘤药物中的应用 | |
| HK40058867A (en) | Imidazopyridinyl compounds and use thereof for treatment of proliferative disorders |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant | ||
| TR01 | Transfer of patent right | ||
| TR01 | Transfer of patent right |
Effective date of registration: 20210604 Address after: Nine Biological Industrial Parks 218 Sangtian Street, Suzhou Industrial Park, Suzhou City, Jiangsu Province Patentee after: Baiji Shenzhou (Suzhou) Biotechnology Co.,Ltd. Address before: Greater Cayman, Cayman Islands Patentee before: BEIGENE, Ltd. |