MA45920B1 - Inhibiteurs de pyridopyrimidinone cdk2/4/6 - Google Patents
Inhibiteurs de pyridopyrimidinone cdk2/4/6Info
- Publication number
- MA45920B1 MA45920B1 MA45920A MA45920A MA45920B1 MA 45920 B1 MA45920 B1 MA 45920B1 MA 45920 A MA45920 A MA 45920A MA 45920 A MA45920 A MA 45920A MA 45920 B1 MA45920 B1 MA 45920B1
- Authority
- MA
- Morocco
- Prior art keywords
- pyridopyrimidinone
- cdk2
- inhibitors
- compounds
- salts
- Prior art date
Links
- IAAQUOVTPAMQCR-UHFFFAOYSA-N 1h-pyrido[3,2-d]pyrimidin-2-one Chemical compound C1=CC=C2NC(=O)N=CC2=N1 IAAQUOVTPAMQCR-UHFFFAOYSA-N 0.000 title 1
- 101150073031 cdk2 gene Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 230000002159 abnormal effect Effects 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 230000010261 cell growth Effects 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic 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
- C07D487/04—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
- C07D471/02—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
-
- 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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
L'invention concerne des composés de formule générale (i), et des sels pharmaceutiquement acceptables de ceux-ci, dans lesquels r1, r2, r2a, r2b, r3, r4, r5a, r5b, r6, r7, r8, r9, p, q et r sont tels que définis dans la description, ainsi que des compositions pharmaceutiques comprenant de tels composés et sels, et sur des procédés d'utilisation de tels composés, sels et compositions pour le traitement d'une croissance cellulaire anormale, y compris le cancer.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201662371602P | 2016-08-15 | 2016-08-15 | |
| US201762533347P | 2017-07-17 | 2017-07-17 | |
| PCT/IB2017/054655 WO2018033815A1 (fr) | 2016-08-15 | 2017-07-31 | Inhibiteurs de pyridopyrimidinone cdk2/4/6 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MA45920A MA45920A (fr) | 2019-06-19 |
| MA45920B1 true MA45920B1 (fr) | 2021-08-31 |
Family
ID=59631834
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA45920A MA45920B1 (fr) | 2016-08-15 | 2017-07-31 | Inhibiteurs de pyridopyrimidinone cdk2/4/6 |
Country Status (43)
Families Citing this family (51)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR112019002610A2 (pt) * | 2016-08-15 | 2019-07-02 | Pfizer | piridopirimidinonas inibidoras de cdk2/4/6 |
| JP6952747B2 (ja) * | 2018-09-18 | 2021-10-20 | ファイザー・インク | がん処置のためのTGFβ阻害剤およびCDK阻害剤の組合せ |
| JP2020097562A (ja) * | 2018-09-25 | 2020-06-25 | ファイザー・インク | ピリド[2,3−d]ピリミジン−7(8h)−オンの合成 |
| US11066404B2 (en) | 2018-10-11 | 2021-07-20 | Incyte Corporation | Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors |
| CA3124330A1 (fr) | 2018-12-21 | 2020-06-25 | Daiichi Sankyo Company, Limited | Combinaison d'un conjugue anticorps-medicament et d'un inhibiteur de kinase |
| US20220127262A1 (en) * | 2019-01-17 | 2022-04-28 | Pfizer Inc. | Crystalline form of a cdk inhibitor |
| US11384083B2 (en) | 2019-02-15 | 2022-07-12 | Incyte Corporation | Substituted spiro[cyclopropane-1,5′-pyrrolo[2,3-d]pyrimidin]-6′(7′h)-ones as CDK2 inhibitors |
| EP3923949A1 (fr) * | 2019-02-15 | 2021-12-22 | Incyte Corporation | Biomarqueurs de kinase 2 dépendant de la cycline et leurs utilisations |
| TW202100520A (zh) | 2019-03-05 | 2021-01-01 | 美商英塞特公司 | 作為cdk2 抑制劑之吡唑基嘧啶基胺化合物 |
| WO2020205560A1 (fr) | 2019-03-29 | 2020-10-08 | Incyte Corporation | Composés sulfonylamides utilisés comme inhibiteurs de la cdk2 |
| EP3956031A1 (fr) * | 2019-04-19 | 2022-02-23 | Pfizer Inc. | Agents antiprolifératifs pour le traitement de l'htap |
| US11440914B2 (en) | 2019-05-01 | 2022-09-13 | Incyte Corporation | Tricyclic amine compounds as CDK2 inhibitors |
| US11447494B2 (en) | 2019-05-01 | 2022-09-20 | Incyte Corporation | Tricyclic amine compounds as CDK2 inhibitors |
| JP2022533833A (ja) | 2019-05-24 | 2022-07-26 | ファイザー・インク | Cdk阻害剤を使用した組合せ療法 |
| WO2020239558A1 (fr) | 2019-05-24 | 2020-12-03 | Pfizer Inc. | Polythérapies faisant appel à des inhibiteurs de cdk |
| WO2021014360A1 (fr) | 2019-07-23 | 2021-01-28 | Pfizer Inc. | Formes posologiques à libération modifiée par voie orale |
| CN116348458A (zh) | 2019-08-14 | 2023-06-27 | 因赛特公司 | 作为cdk2抑制剂的咪唑基嘧啶基胺化合物 |
| CN119930611A (zh) | 2019-10-11 | 2025-05-06 | 因赛特公司 | 作为cdk2抑制剂的双环胺 |
| JP7667147B2 (ja) * | 2019-10-17 | 2025-04-22 | シーセン ファーマシューティカル カンパニー リミテッド | Cdk2/4/6三重阻害剤としてのアミノピリミジン化合物 |
| US11702474B2 (en) | 2019-12-17 | 2023-07-18 | Pfizer Inc. | Antibodies specific for CD47, PD-L1, and uses thereof |
| JP2023515629A (ja) * | 2020-02-28 | 2023-04-13 | フォチョン・バイオサイエンシーズ・リミテッド | Cdk2/4/6阻害剤としての化合物 |
| WO2021176349A1 (fr) | 2020-03-05 | 2021-09-10 | Pfizer Inc. | Combinaison d'un inhibiteur de kinase du lymphome anaplasique et d'un inhibiteur de kinase dépendant de la cycline |
| JP2021167301A (ja) | 2020-04-08 | 2021-10-21 | ファイザー・インク | Cdk2阻害剤に対する腫瘍適応を抑制するためのcdk4/6およびcdk2阻害剤による同時処置 |
| CN113773315A (zh) * | 2020-06-10 | 2021-12-10 | 无锡佰翱得生物科学有限公司 | 细胞周期蛋白依赖性激酶2(cdk2)高选择性氘代抑制剂 |
| CN115702155B (zh) * | 2020-06-17 | 2025-01-24 | 微境生物医药科技(上海)有限公司 | 新型吡啶并[2,3-d]嘧啶-7(8H)-酮衍生物 |
| WO2022015670A1 (fr) * | 2020-07-14 | 2022-01-20 | Nikang Therapeutics, Inc. | Dérivés de pyrido[2,3-d]pyrimidin-7(8h)-one utilisés en tant qu'inhibiteurs de kinase 2 dépendant de la cycline |
| WO2022018667A1 (fr) | 2020-07-24 | 2022-01-27 | Pfizer Inc. | Polythérapies utilisant des inhibiteurs de cdk2 et de cdc25a |
| MX2023003054A (es) | 2020-09-15 | 2023-04-05 | Pfizer | Formas solidas de un inhibidor de cdk4. |
| WO2022113003A1 (fr) | 2020-11-27 | 2022-06-02 | Rhizen Pharmaceuticals Ag | Inhibiteurs de cdk |
| IL303661A (en) * | 2020-12-22 | 2023-08-01 | Nikang Therapeutics Inc | Compounds for degrading cyclin-dependent kinase 2 via ubiquitin proteosome pathway |
| WO2022149057A1 (fr) | 2021-01-05 | 2022-07-14 | Rhizen Pharmaceuticals Ag | Inhibiteurs de cdk |
| CN117858879A (zh) * | 2021-01-15 | 2024-04-09 | 南京再明医药有限公司 | Cdk2/4/6抑制剂及其制备方法和应用 |
| AU2022271290A1 (en) | 2021-05-07 | 2023-11-23 | Kymera Therapeutics, Inc. | Cdk2 degraders and uses thereof |
| US20240287065A1 (en) * | 2021-06-09 | 2024-08-29 | Tyk Medicines (Zhengzhou) , Inc. | Compound as cdk kinase inhibitor and use thereof |
| US11981671B2 (en) | 2021-06-21 | 2024-05-14 | Incyte Corporation | Bicyclic pyrazolyl amines as CDK2 inhibitors |
| WO2023281413A1 (fr) | 2021-07-09 | 2023-01-12 | Pfizer Inc. | Méthodes et schémas posologiques comprenant pf-06873600 pour le traitement du cancer |
| WO2023051302A1 (fr) * | 2021-09-29 | 2023-04-06 | 中国医药研究开发中心有限公司 | Composé hétérocyclique ayant une activité inhibitrice de kinase cycline-dépendante, son procédé de préparation et son utilisation médicale |
| JP2024542205A (ja) * | 2021-11-18 | 2024-11-13 | オンコノヴァ セラピューティクス, インコーポレイテッド | がんを処置するための方法および組成物 |
| US11976073B2 (en) | 2021-12-10 | 2024-05-07 | Incyte Corporation | Bicyclic amines as CDK2 inhibitors |
| WO2023111810A1 (fr) | 2021-12-14 | 2023-06-22 | Pfizer Inc. | Polythérapies et leurs utilisations pour le traitement du cancer |
| WO2023141522A2 (fr) * | 2022-01-21 | 2023-07-27 | Slap Pharmaceuticals Llc | Composés multicycliques |
| JP2025508323A (ja) * | 2022-01-25 | 2025-03-26 | キネート バイオファーマ インク. | Cdk4/6キナーゼの阻害薬 |
| AU2023289896A1 (en) * | 2022-06-22 | 2024-12-05 | Nikang Therapeutics, Inc. | Bifunctional compounds containing pyrido[2,3-djpyrimidin-7(8h)-one derivatives for degrading cyclin-dependent kinase 2 via ubiquitin proteasome pathway |
| EP4573094A2 (fr) * | 2022-08-19 | 2025-06-25 | Kymera Therapeutics, Inc. | Inhibiteurs de cdk2 et utilisations associées |
| CN120379671A (zh) | 2022-10-18 | 2025-07-25 | 辉瑞公司 | 用于治疗癌症的化合物 |
| WO2024173766A1 (fr) * | 2023-02-17 | 2024-08-22 | Differentiated Therapeutics, Inc. | Agents de dégradation de kinase dépendant de la cycline et leurs méthodes d'utilisation |
| CR20250545A (es) | 2023-06-01 | 2026-01-15 | H Lundbeck As | Agonistas espiromacrocíclicos de receptores de orexina 2 |
| WO2025175258A1 (fr) * | 2024-02-17 | 2025-08-21 | Padarn Therapeutics, Inc. | Inhibiteurs de cdk2 |
| WO2025207957A1 (fr) * | 2024-03-28 | 2025-10-02 | Yale University | Inhibiteurs de pi5p4k alpha/bêta à petites molécules et procédés les utilisant |
| CN120842218A (zh) * | 2024-04-26 | 2025-10-28 | 郑州同源康医药有限公司 | 一种嘧啶并氮杂环类化合物的晶型及其制备方法及应用 |
| WO2026024674A1 (fr) | 2024-07-22 | 2026-01-29 | Genesis Therapeutics, Inc. | Méthodes de traitement de cancers associés à skp2 |
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2017
- 2017-07-31 BR BR112019002610A patent/BR112019002610A2/pt active Search and Examination
- 2017-07-31 DK DK17752493.1T patent/DK3497103T3/da active
- 2017-07-31 HU HUE17752493A patent/HUE055978T2/hu unknown
- 2017-07-31 MD MDE20190682T patent/MD3497103T2/ro unknown
- 2017-07-31 JP JP2019507917A patent/JP6563623B1/ja not_active Expired - Fee Related
- 2017-07-31 CA CA2975033A patent/CA2975033C/fr active Active
- 2017-07-31 EP EP17752493.1A patent/EP3497103B1/fr active Active
- 2017-07-31 CU CU2019000010A patent/CU24522B1/es unknown
- 2017-07-31 GE GEAP201714998A patent/GEP20217234B/en unknown
- 2017-07-31 SI SI201730793T patent/SI3497103T1/sl unknown
- 2017-07-31 PE PE2019000359A patent/PE20190475A1/es unknown
- 2017-07-31 PT PT177524931T patent/PT3497103T/pt unknown
- 2017-07-31 MA MA45920A patent/MA45920B1/fr unknown
- 2017-07-31 CN CN202210092651.2A patent/CN114394966B/zh active Active
- 2017-07-31 HR HRP20210871TT patent/HRP20210871T1/hr unknown
- 2017-07-31 WO PCT/IB2017/054655 patent/WO2018033815A1/fr not_active Ceased
- 2017-07-31 ES ES17752493T patent/ES2876411T3/es active Active
- 2017-07-31 NZ NZ750410A patent/NZ750410A/en unknown
- 2017-07-31 MY MYPI2019000748A patent/MY198534A/en unknown
- 2017-07-31 RU RU2019104087A patent/RU2726115C1/ru active
- 2017-07-31 RS RS20210691A patent/RS61934B1/sr unknown
- 2017-07-31 TN TNP/2019/000039A patent/TN2019000039A1/en unknown
- 2017-07-31 KR KR1020197007466A patent/KR102236605B1/ko not_active Expired - Fee Related
- 2017-07-31 CR CR20190062A patent/CR20190062A/es unknown
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- 2017-07-31 US US15/664,265 patent/US10233188B2/en active Active
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- 2017-07-31 UA UAA201900905A patent/UA124804C2/uk unknown
- 2017-07-31 AU AU2017311645A patent/AU2017311645B2/en not_active Ceased
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2019
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2020
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2021
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2022
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