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 (55)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109803968A (zh) * | 2016-08-15 | 2019-05-24 | 辉瑞公司 | 吡啶并嘧啶酮cdk2/4/6抑制剂 |
| 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 |
| BR112021011894A2 (pt) | 2018-12-21 | 2021-09-08 | Daiichi Sankyo Company, Limited | Composição farmacêutica |
| CN113260617A (zh) * | 2019-01-17 | 2021-08-13 | 辉瑞公司 | Cdk抑制剂的结晶形式 |
| WO2020168197A1 (fr) | 2019-02-15 | 2020-08-20 | Incyte Corporation | Composés de pyrrolo[2,3-d]pyrimidinone en tant qu'inhibiteurs de cdk2 |
| EA202192260A1 (ru) * | 2019-02-15 | 2021-12-17 | Инсайт Корпорейшн | Биомаркеры циклин-зависимой киназы 2 и их применение |
| 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 |
| US11919904B2 (en) | 2019-03-29 | 2024-03-05 | Incyte Corporation | Sulfonylamide compounds as CDK2 inhibitors |
| AU2020260018A1 (en) | 2019-04-19 | 2021-11-04 | Pfizer Inc. | Anti-proliferative agents for treating PAH |
| WO2020223558A1 (fr) | 2019-05-01 | 2020-11-05 | Incyte Corporation | Composés aminés tricycliques en tant qu'inhibiteurs de cdk2 |
| WO2020223469A1 (fr) | 2019-05-01 | 2020-11-05 | Incyte Corporation | Dérivés de n-(1-(méthylsulfonyl)pipéridin-4-yl)-4,5-di hydro-1h-imidazo[4,5-h]quinazolin-8-amine et composés apparentés utilisés en tant qu'inhibiteurs de kinase 2 dépendante des cyclines (cdk2) pour le traitement du cancer |
| US20220241412A1 (en) | 2019-05-24 | 2022-08-04 | Pfizer Inc. | Combination therapies using cdk inhibitors |
| WO2020240360A1 (fr) | 2019-05-24 | 2020-12-03 | Pfizer Inc. | Polythérapies à l'aide d'inhibiteurs cdk |
| WO2021014360A1 (fr) | 2019-07-23 | 2021-01-28 | Pfizer Inc. | Formes posologiques à libération modifiée par voie orale |
| WO2021030537A1 (fr) | 2019-08-14 | 2021-02-18 | Incyte Corporation | Composés imidazolyl-pyrimidinylamines utilisés comme inhibiteurs de la cdk2 |
| CR20220170A (es) * | 2019-10-11 | 2022-10-10 | Incyte Corp | Aminas bicíclicas como inhibidoras de la cdk2 |
| 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 |
| JP7369297B2 (ja) | 2019-12-17 | 2023-10-25 | ファイザー・インク | Cd47、pd-l1に特異的な抗体、およびその使用 |
| 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 |
| TW202146017A (zh) * | 2020-03-05 | 2021-12-16 | 美商輝瑞股份有限公司 | 間變性淋巴瘤激酶抑制劑及周期蛋白依賴型激酶抑制劑之組合 |
| 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. |
| EP4217356B1 (fr) | 2020-09-25 | 2025-05-14 | JANSSEN Pharmaceutica NV | Inhibiteurs non covalents de la kinase cycline-dépendante 7 (cdk7) |
| WO2022113003A1 (fr) | 2020-11-27 | 2022-06-02 | Rhizen Pharmaceuticals Ag | Inhibiteurs de cdk |
| CN116783205A (zh) * | 2020-12-22 | 2023-09-19 | 尼坎治疗公司 | 用于通过泛素蛋白酶体途径降解细胞周期蛋白依赖性激酶2的化合物 |
| AU2021409561A1 (en) * | 2020-12-22 | 2023-07-06 | 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 |
| CA3217792A1 (fr) | 2021-05-07 | 2022-11-10 | Kymera Therapeutics, Inc | Agents de degradation de cdk2 et leurs utilisations |
| JP7822578B2 (ja) * | 2021-06-09 | 2026-03-03 | ティーワイケー メディシンズ(ジョンジョウ),インコーポレーテッド | Cdkキナーゼ阻害剤として使用される化合物およびその応用 |
| 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 |
| IL312844A (en) * | 2021-11-18 | 2024-07-01 | Onconova Therapeutics Inc | Methods and compositions for treating cancer |
| US11976073B2 (en) | 2021-12-10 | 2024-05-07 | Incyte Corporation | Bicyclic amines as CDK2 inhibitors |
| US20250049802A1 (en) | 2021-12-14 | 2025-02-13 | Pfizer Inc. | Combination therapies and uses for treating cancer |
| WO2023141522A2 (fr) * | 2022-01-21 | 2023-07-27 | Slap Pharmaceuticals Llc | Composés multicycliques |
| AU2023212957A1 (en) * | 2022-01-25 | 2024-08-22 | Kinnate Biopharma Inc. | Inhibitors of cdk4/6 kinase |
| CN119451967A (zh) * | 2022-06-22 | 2025-02-14 | 霖康疗法公司 | 用于经由泛素蛋白酶体途径降解细胞周期蛋白依赖性激酶2的含有吡啶并[2,3-d]嘧啶-7(8H)-酮衍生物的双功能化合物 |
| US20240174665A1 (en) * | 2022-08-19 | 2024-05-30 | Kymera Therapeutics, Inc. | Cdk2 inhibitors and uses thereof |
| EP4604961A1 (fr) | 2022-10-18 | 2025-08-27 | Pfizer Inc. | Composés pour le traitement du cancer |
| 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 |
| JP2026518313A (ja) | 2023-06-01 | 2026-06-04 | ハー・ルンドベック・アクチエゼルスカベット | スピロ大環状オレキシン2受容体アゴニスト |
| AU2025220986A1 (en) * | 2024-02-17 | 2026-08-13 | Padarn Therapeutics, Inc. | Inhibitors of 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 |
| WO2026114911A1 (fr) | 2024-11-27 | 2026-06-04 | H. Lundbeck A/S | Agonistes du récepteur 2 de l'oréxine |
| US20260144795A1 (en) | 2024-11-27 | 2026-05-28 | H. Lundbeck A/S | Spiromacrocyclic orexin 2 receptor agonists |
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-
2017
- 2017-07-31 CN CN201780063655.5A patent/CN109803968A/zh active Pending
- 2017-07-31 NZ NZ750410A patent/NZ750410A/en unknown
- 2017-07-31 BR BR112019002610A patent/BR112019002610A2/pt active Search and Examination
- 2017-07-31 MD MDE20190682T patent/MD3497103T2/ro unknown
- 2017-07-31 UA UAA201900905A patent/UA124804C2/uk unknown
- 2017-07-31 MY MYPI2019000748A patent/MY198534A/en unknown
- 2017-07-31 WO PCT/IB2017/054655 patent/WO2018033815A1/fr not_active Ceased
- 2017-07-31 CR CR20190062A patent/CR20190062A/es unknown
- 2017-07-31 DK DK17752493.1T patent/DK3497103T3/da active
- 2017-07-31 PL PL17752493T patent/PL3497103T3/pl unknown
- 2017-07-31 PE PE2019000359A patent/PE20190475A1/es unknown
- 2017-07-31 CN CN202210092651.2A patent/CN114394966B/zh not_active Expired - Fee Related
- 2017-07-31 MX MX2019001849A patent/MX389597B/es unknown
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