LT2632467T - Cdk inhibitoriai - Google Patents
Cdk inhibitoriaiInfo
- Publication number
- LT2632467T LT2632467T LTEP11838545.9T LT11838545T LT2632467T LT 2632467 T LT2632467 T LT 2632467T LT 11838545 T LT11838545 T LT 11838545T LT 2632467 T LT2632467 T LT 2632467T
- Authority
- LT
- Lithuania
- Prior art keywords
- cdk inhibitors
- cdk
- inhibitors
- Prior art date
Links
- 229940043378 cyclin-dependent kinase inhibitor Drugs 0.000 title 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
- C07D487/12—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 three hetero rings
- C07D487/20—Spiro-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
- A61K31/499—Spiro-condensed pyrazines or piperazines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
- C07D487/12—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 three hetero rings
- C07D487/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Indole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US40649810P | 2010-10-25 | 2010-10-25 | |
| PCT/US2011/057749 WO2012061156A1 (en) | 2010-10-25 | 2011-10-25 | Cdk inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| LT2632467T true LT2632467T (lt) | 2016-09-12 |
Family
ID=46024778
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LTEP11838545.9T LT2632467T (lt) | 2010-10-25 | 2011-10-25 | Cdk inhibitoriai |
Country Status (25)
| Country | Link |
|---|---|
| US (2) | US8598197B2 (OSRAM) |
| EP (6) | EP2632467B1 (OSRAM) |
| JP (4) | JP5923509B2 (OSRAM) |
| KR (4) | KR101929593B1 (OSRAM) |
| CN (5) | CN103936745B (OSRAM) |
| AU (5) | AU2011323739B2 (OSRAM) |
| BR (1) | BR112013010018B1 (OSRAM) |
| CA (2) | CA2961937C (OSRAM) |
| CY (1) | CY1118004T1 (OSRAM) |
| DK (1) | DK2632467T3 (OSRAM) |
| ES (1) | ES2592515T3 (OSRAM) |
| HK (2) | HK1197067A1 (OSRAM) |
| HR (1) | HRP20161092T1 (OSRAM) |
| HU (1) | HUE030714T2 (OSRAM) |
| IL (5) | IL225940A0 (OSRAM) |
| LT (1) | LT2632467T (OSRAM) |
| MX (4) | MX379532B (OSRAM) |
| PL (1) | PL2632467T3 (OSRAM) |
| PT (1) | PT2632467T (OSRAM) |
| RS (1) | RS55135B1 (OSRAM) |
| RU (1) | RU2621674C2 (OSRAM) |
| SG (2) | SG10201508715YA (OSRAM) |
| SI (1) | SI2632467T1 (OSRAM) |
| SM (1) | SMT201600311B (OSRAM) |
| WO (1) | WO2012061156A1 (OSRAM) |
Families Citing this family (121)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101212967A (zh) | 2005-05-10 | 2008-07-02 | 因塞特公司 | 吲哚胺2,3-双加氧酶调节剂及其用法 |
| CN104042611B (zh) | 2008-07-08 | 2019-05-14 | 因塞特控股公司 | 作为吲哚胺2，3-双加氧酶的抑制剂的1，2，5-噁二唑 |
| EP3406260B1 (en) | 2009-05-13 | 2020-09-23 | The University of North Carolina at Chapel Hill | Cyclin dependent kinase inhibitors and methods of use |
| US8691830B2 (en) | 2010-10-25 | 2014-04-08 | G1 Therapeutics, Inc. | CDK inhibitors |
| CN103501789A (zh) | 2010-11-17 | 2014-01-08 | 北卡罗来纳大学查珀尔希尔分校 | 通过抑制增殖性激酶cdk4和cdk6保护肾组织免于局部缺血 |
| CA2868966C (en) | 2012-03-29 | 2021-01-26 | Francis Xavier Tavares | Lactam kinase inhibitors |
| US10202392B2 (en) * | 2012-04-26 | 2019-02-12 | Francis Xavier Tavares | Synthesis of lactams |
| EP3495367B1 (en) | 2012-06-13 | 2020-09-30 | Incyte Holdings Corporation | Substituted tricyclic compounds as fgfr inhibitors |
| ES2761406T3 (es) | 2013-03-15 | 2020-05-19 | G1 Therapeutics Inc | Protección transitoria de células normales durante una quimioterapia |
| US20140274896A1 (en) * | 2013-03-15 | 2014-09-18 | G1 Therapeutics, Inc. | Transient Protection of Hematopoietic Stem and Progenitor Cells Against Ionizing Radiation |
| US20140271460A1 (en) | 2013-03-15 | 2014-09-18 | G1 Therapeutics, Inc. | Highly Active Anti-Neoplastic and Anti-Proliferative Agents |
| DK2986610T5 (en) | 2013-04-19 | 2018-12-10 | Incyte Holdings Corp | BICYCLIC HETEROCYCLES AS FGFR INHIBITORS |
| WO2015161288A1 (en) * | 2014-04-17 | 2015-10-22 | G1 Therapeutics, Inc. | Tricyclic lactams for use as anti-neoplastic and anti-proliferative agents |
| WO2016040848A1 (en) * | 2014-09-12 | 2016-03-17 | G1 Therapeutics, Inc. | Treatment of rb-negative tumors using topoisomerase inhibitors in combination with cyclin dependent kinase 4/6 inhibitors |
| EP3191098A4 (en) | 2014-09-12 | 2018-04-25 | G1 Therapeutics, Inc. | Combinations and dosing regimes to treat rb-positive tumors |
| US20160220569A1 (en) * | 2015-02-03 | 2016-08-04 | G1 Therapeutics, Inc. | CDK4/6 Inhibitor Dosage Formulations For The Protection Of Hematopoietic Stem And Progenitor Cells During Chemotherapy |
| CR20170390A (es) | 2015-02-20 | 2017-10-23 | Incyte Holdings Corp | Heterociclos biciclicos como inhibidores de fgfr |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| MX2019000200A (es) * | 2016-07-01 | 2019-09-26 | G1 Therapeutics Inc | Agentes antiproliferativos basados en pirimidina. |
| WO2018005533A1 (en) | 2016-07-01 | 2018-01-04 | G1 Therapeutics, Inc. | Antiproliferative pyrimidine-based compounds |
| WO2018005863A1 (en) * | 2016-07-01 | 2018-01-04 | G1 Therapeutics, Inc. | Pyrimidine-based compounds for the treatment of cancer |
| NZ749275A (en) | 2016-07-01 | 2023-06-30 | G1 Therapeutics Inc | Synthesis of n-(heteroaryl)-pyrrolo[2,3-d]pyrimidin-2-amines |
| RU2769251C2 (ru) | 2016-08-23 | 2022-03-29 | Эйсай Ар Энд Ди Менеджмент Ко., Лтд. | Комбинированная терапия для лечения гепатоцеллюлярной карциномы |
| CA3040815C (en) | 2016-10-20 | 2021-07-20 | Steven Martin Evans | Anti-proliferative agents for treating pah |
| WO2018089518A1 (en) | 2016-11-08 | 2018-05-17 | Dana-Farber Cancer Institute, Inc. | Compositions and methods of modulating anti-tumor immunity |
| CN113264935B (zh) * | 2016-11-11 | 2022-09-20 | 上海海雁医药科技有限公司 | 吡啶胺取代的杂三环化合物及其中间体和医药上的用途 |
| CN117530948A (zh) | 2016-12-05 | 2024-02-09 | G1治疗公司 | 化疗方案期间免疫反应的保持 |
| EA201991622A1 (ru) | 2017-01-06 | 2020-01-23 | Г1 Терапьютикс, Инк. | Комплексная терапия для лечения рака |
| US11395821B2 (en) | 2017-01-30 | 2022-07-26 | G1 Therapeutics, Inc. | Treatment of EGFR-driven cancer with fewer side effects |
| WO2018156812A1 (en) | 2017-02-22 | 2018-08-30 | G1 Therapeutics, Inc. | Treatment of egfr-driven cancer with fewer side effects |
| EP3595725B1 (en) | 2017-03-16 | 2023-05-03 | Eisai R&D Management Co., Ltd. | Combination therapies for the treatment of breast cancer |
| AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
| KR102659211B1 (ko) | 2017-06-29 | 2024-04-18 | 쥐원 쎄라퓨틱스, 인크. | G1t38의 형체 형태 및 그의 제조 방법 |
| CN107383019B (zh) * | 2017-07-28 | 2019-10-15 | 江苏艾凡生物医药有限公司 | 吡唑并[4,3-h]喹唑啉类化合物及其用途 |
| CN109985241B (zh) * | 2017-12-29 | 2024-10-18 | 广州威溶特医药科技有限公司 | Cdk抑制剂和溶瘤病毒在制备抗肿瘤药物的应用 |
| MY205589A (en) | 2018-01-08 | 2024-10-28 | G1 Therapeutics Inc | G1t38 superior dosage regimes |
| CA3092470A1 (en) | 2018-02-27 | 2019-09-06 | Incyte Corporation | Imidazopyrimidines and triazolopyrimidines as a2a / a2b inhibitors |
| US11466004B2 (en) | 2018-05-04 | 2022-10-11 | Incyte Corporation | Solid forms of an FGFR inhibitor and processes for preparing the same |
| CN112566912A (zh) | 2018-05-04 | 2021-03-26 | 因赛特公司 | Fgfr抑制剂的盐 |
| WO2019222677A1 (en) | 2018-05-18 | 2019-11-21 | Incyte Corporation | Fused pyrimidine derivatives as a2a / a2b inhibitors |
| AU2019297361B2 (en) | 2018-07-05 | 2024-06-27 | Incyte Corporation | Fused pyrazine derivatives as A2A / A2B inhibitors |
| EP3840756B1 (en) | 2018-08-24 | 2025-11-05 | Pharmacosmos Holding A/S | Improved synthesis of 1,4-diazaspiro[5.5]undecan-3-one |
| WO2020055758A1 (en) | 2018-09-10 | 2020-03-19 | Mirati Therapeutics, Inc. | Combination therapies |
| US11066404B2 (en) | 2018-10-11 | 2021-07-20 | Incyte Corporation | Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors |
| CN113271977A (zh) * | 2018-11-09 | 2021-08-17 | G1治疗公司 | 使用艾日布林和选择性cdk4/6抑制剂组合治疗癌症的治疗方案 |
| AU2019407426A1 (en) | 2018-12-21 | 2021-07-22 | Daiichi Sankyo Company, Limited | Combination of antibody-drug conjugate and kinase inhibitor |
| CN111377924A (zh) * | 2018-12-29 | 2020-07-07 | 武汉光谷通用名药物研究院有限公司 | 新型cdk4抑制剂及其用途 |
| CN111377935B (zh) * | 2018-12-29 | 2021-06-29 | 武汉光谷通用名药物研究院有限公司 | 选择性cdk4/6抑制剂及其应用 |
| TWI829857B (zh) | 2019-01-29 | 2024-01-21 | 美商英塞特公司 | 作為a2a / a2b抑制劑之吡唑并吡啶及三唑并吡啶 |
| MA54947A (fr) | 2019-02-15 | 2021-12-22 | Incyte Corp | Biomarqueurs de kinase 2 dépendant de la cycline et leurs utilisations |
| WO2020168197A1 (en) | 2019-02-15 | 2020-08-20 | Incyte Corporation | Pyrrolo[2,3-d]pyrimidinone compounds as cdk2 inhibitors |
| WO2020180959A1 (en) | 2019-03-05 | 2020-09-10 | Incyte Corporation | Pyrazolyl pyrimidinylamine compounds as cdk2 inhibitors |
| WO2020185532A1 (en) | 2019-03-08 | 2020-09-17 | Incyte Corporation | Methods of treating cancer with an fgfr inhibitor |
| WO2020205560A1 (en) | 2019-03-29 | 2020-10-08 | Incyte Corporation | Sulfonylamide compounds as cdk2 inhibitors |
| 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 |
| US11591329B2 (en) | 2019-07-09 | 2023-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| CN114502196A (zh) | 2019-08-01 | 2022-05-13 | 因赛特公司 | Ido抑制剂的给药方案 |
| PH12022550361A1 (en) | 2019-08-14 | 2023-02-27 | Incyte Corp | Imidazolyl pyrimidinylamine compounds as cdk2 inhibitors |
| US12122767B2 (en) | 2019-10-01 | 2024-10-22 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| MX2022004390A (es) | 2019-10-11 | 2022-08-08 | Incyte Corp | Aminas biciclicas como inhibidores de la cinasa dependiente de ciclina 2 (cdk2). |
| GEAP202415945A (en) | 2019-10-14 | 2024-04-25 | Incyte Corp | Bicyclic heterocycles as fgfr inhibitors |
| WO2021076728A1 (en) | 2019-10-16 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| EP4069696A1 (en) | 2019-12-04 | 2022-10-12 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| BR112022010664A2 (pt) | 2019-12-04 | 2022-08-16 | Incyte Corp | Derivados de um inibidor de fgfr |
| US12012409B2 (en) | 2020-01-15 | 2024-06-18 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| AU2021230385A1 (en) | 2020-03-06 | 2022-09-22 | Incyte Corporation | Combination therapy comprising AXL/MER and PD-1/PD-L1 inhibitors |
| 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 |
| EP4135844A1 (en) | 2020-04-16 | 2023-02-22 | Incyte Corporation | Fused tricyclic kras inhibitors |
| US11739102B2 (en) | 2020-05-13 | 2023-08-29 | Incyte Corporation | Fused pyrimidine compounds as KRAS inhibitors |
| KR20230012547A (ko) | 2020-05-19 | 2023-01-26 | 쥐원 쎄라퓨틱스, 인크. | 의학적 장애의 치료를 위한 시클린-의존성 키나제 억제 화합물 |
| MX2022015567A (es) | 2020-06-11 | 2023-01-19 | Lunella Biotech Inc | Productos terapeuticos contra el cancer de inhibidores selectivos de cdk4/6. |
| CN116157403B (zh) * | 2020-06-15 | 2025-04-25 | 海南先声再明医药股份有限公司 | 曲拉西利的形态及其制造方法 |
| US10988479B1 (en) | 2020-06-15 | 2021-04-27 | G1 Therapeutics, Inc. | Morphic forms of trilaciclib and methods of manufacture thereof |
| WO2022047093A1 (en) | 2020-08-28 | 2022-03-03 | Incyte Corporation | Vinyl imidazole compounds as inhibitors of kras |
| US11767320B2 (en) | 2020-10-02 | 2023-09-26 | Incyte Corporation | Bicyclic dione compounds as inhibitors of KRAS |
| WO2022076779A1 (en) * | 2020-10-08 | 2022-04-14 | Teva Pharmaceuticals International Gmbh | Solid state forms of trilaciclib and of trilaciclib salts |
| WO2022155941A1 (en) | 2021-01-25 | 2022-07-28 | Qilu Regor Therapeutics Inc. | Cdk2 inhibitors |
| WO2022206888A1 (en) | 2021-03-31 | 2022-10-06 | Qilu Regor Therapeutics Inc. | Cdk2 inhibitors and use thereof |
| TW202304459A (zh) | 2021-04-12 | 2023-02-01 | 美商英塞特公司 | 包含ｆｇｆｒ抑制劑及ｎｅｃｔｉｎ－４靶向劑之組合療法 |
| WO2022261159A1 (en) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| JP2024522189A (ja) | 2021-06-09 | 2024-06-11 | インサイト・コーポレイション | Ｆｇｆｒ阻害剤としての三環式ヘテロ環 |
| US11981671B2 (en) | 2021-06-21 | 2024-05-14 | Incyte Corporation | Bicyclic pyrazolyl amines as CDK2 inhibitors |
| US12441727B2 (en) | 2021-07-07 | 2025-10-14 | Incyte Corporation | Tricyclic compounds as inhibitors of KRAS |
| CA3224841A1 (en) | 2021-07-14 | 2023-01-19 | Zhenwu Li | Tricyclic compounds as inhibitors of kras |
| CA3227191A1 (en) | 2021-07-26 | 2023-02-02 | Celcuity Inc. | 1-(4-{[4-(dimethylamino)piperidin-1-yl]carbonyl}phenyl)-3-[4-(4,6-dimorpholin-4-yl-1,3,5-triazin-2-yl)phenyl]urea (gedatolisib) and its combinations for use in the treatment of cancer |
| CN113788837B (zh) * | 2021-08-02 | 2022-08-26 | 深圳湾实验室坪山生物医药研发转化中心 | Trilaciclib的合成方法 |
| CA3229855A1 (en) | 2021-08-31 | 2023-03-09 | Incyte Corporation | Naphthyridine compounds as inhibitors of kras |
| US12030883B2 (en) | 2021-09-21 | 2024-07-09 | Incyte Corporation | Hetero-tricyclic compounds as inhibitors of KRAS |
| WO2023056421A1 (en) | 2021-10-01 | 2023-04-06 | Incyte Corporation | Pyrazoloquinoline kras inhibitors |
| PE20242113A1 (es) | 2021-10-14 | 2024-10-28 | Incyte Corp | Compuestos de quinolina como inhibidores de kras |
| WO2023091746A1 (en) | 2021-11-22 | 2023-05-25 | Incyte Corporation | Combination therapy comprising an fgfr inhibitor and a kras inhibitor |
| TW202329937A (zh) | 2021-12-03 | 2023-08-01 | 美商英塞特公司 | 雙環胺ｃｋ１２抑制劑 |
| US11976073B2 (en) | 2021-12-10 | 2024-05-07 | Incyte Corporation | Bicyclic amines as CDK2 inhibitors |
| WO2023107705A1 (en) | 2021-12-10 | 2023-06-15 | Incyte Corporation | Bicyclic amines as cdk12 inhibitors |
| WO2023122134A1 (en) | 2021-12-22 | 2023-06-29 | Incyte Corporation | Salts and solid forms of an fgfr inhibitor and processes of preparing thereof |
| TW202341982A (zh) | 2021-12-24 | 2023-11-01 | 大陸商上海齊魯銳格醫藥研發有限公司 | Ｃｄｋ２抑制劑及其用途 |
| WO2023168686A1 (en) | 2022-03-11 | 2023-09-14 | Qilu Regor Therapeutics Inc. | Substituted cyclopentanes as cdk2 inhibitors |
| EP4486458A1 (en) | 2022-02-28 | 2025-01-08 | Teva Pharmaceuticals International GmbH | Crystalline forms of trilaciclib and trilaciclib salts |
| AU2023232823A1 (en) | 2022-03-07 | 2024-09-12 | Incyte Corporation | Solid forms, salts, and processes of preparation of a cdk2 inhibitor |
| US20250353842A1 (en) | 2022-06-22 | 2025-11-20 | Incyte Corporation | Bicyclic amine cdk12 inhibitors |
| US20240101557A1 (en) | 2022-07-11 | 2024-03-28 | Incyte Corporation | Fused tricyclic compounds as inhibitors of kras g12v mutants |
| CN115536663A (zh) * | 2022-10-11 | 2022-12-30 | 杭州科巢生物科技有限公司 | 一种曲拉西利中间体及其制备与应用 |
| EP4626866A1 (en) * | 2022-11-28 | 2025-10-08 | Assia Chemical Industries Ltd. | Novel trilaciclib intermediates, method of preparation and use thereof |
| US20240390340A1 (en) | 2023-04-18 | 2024-11-28 | Incyte Corporation | Pyrrolidine kras inhibitors |
| US20240368156A1 (en) | 2023-04-18 | 2024-11-07 | Incyte Corporation | 2-azabicyclo[2.2.1]heptane kras inhibitors |
| AU2024265078A1 (en) | 2023-05-04 | 2025-12-11 | Revolution Medicines, Inc. | Combination therapy for a ras related disease or disorder |
| IT202300010182A1 (it) | 2023-05-19 | 2024-11-19 | Olon Spa | Forma solvata di trilaciclib di-cloridrato. |
| IT202300010824A1 (it) * | 2023-05-29 | 2024-11-29 | Olon Spa | Forma solvata di trilaciclib di-cloridrato. |
| WO2024246713A1 (en) * | 2023-05-29 | 2024-12-05 | Fresenius Kabi Oncology Ltd | A process for the preparation of cdk inhibiting pyrrolopyrimidine compounds |
| WO2024254245A1 (en) | 2023-06-09 | 2024-12-12 | Incyte Corporation | Bicyclic amines as cdk2 inhibitors |
| US20250049810A1 (en) | 2023-08-07 | 2025-02-13 | Revolution Medicines, Inc. | Methods of treating a ras protein-related disease or disorder |
| CN117069663B (zh) * | 2023-08-31 | 2023-12-26 | 四川维亚本苑生物科技有限公司 | 一种瑞博西尼中间体v的合成方法及瑞博西尼的合成方法 |
| WO2025080946A2 (en) | 2023-10-12 | 2025-04-17 | Revolution Medicines, Inc. | Ras inhibitors |
| US20250163079A1 (en) | 2023-11-01 | 2025-05-22 | Incyte Corporation | Kras inhibitors |
| US20250195536A1 (en) | 2023-12-13 | 2025-06-19 | Incyte Corporation | Bicyclooctane kras inhibitors |
| WO2025134057A1 (en) | 2023-12-20 | 2025-06-26 | Assia Chemical Industries Ltd. | Solid state forms of trilaciclib citrate salt |
| 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 |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2091986C (en) * | 1990-10-09 | 1995-11-28 | Andrew Thurkauf | Certain cycloalkyl and azacycloalkyl pyrrolopyrimidines; a new class of gaba brain receptor ligands |
| GB9718913D0 (en) | 1997-09-05 | 1997-11-12 | Glaxo Group Ltd | Substituted oxindole derivatives |
| EA012926B1 (ru) * | 2001-12-20 | 2010-02-26 | Оси Фармасьютикалз, Инк. | Пирролопиримидиновые соединения, относящиеся к a-селективным антагонистам, их синтез и применение |
| KR20060111716A (ko) | 2002-01-22 | 2006-10-27 | 워너-램버트 캄파니 엘엘씨 | 2-(피리딘-2-일아미노)-피리도[2,3-ｄ]피리미딘-7-온 |
| WO2003070236A2 (en) * | 2002-02-19 | 2003-08-28 | Pharmacia Italia S.P.A. | Tricyclic pyrazole derivatives, process for their preparation and their use as antitumor agents |
| WO2004065378A1 (en) | 2003-01-17 | 2004-08-05 | Warner-Lambert Company Llc | 2-aminopyridine substituted heterocycles as inhibitors of cellular proliferation |
| JP5043432B2 (ja) * | 2003-05-22 | 2012-10-10 | ネルビアーノ・メデイカル・サイエンシーズ・エツセ・エルレ・エルレ | ピラゾロ−キナゾリン誘導体、その製造方法、およびキナーゼ阻害剤としてのその使用 |
| AU2004283843B2 (en) | 2003-10-23 | 2010-04-22 | F. Hoffmann-La Roche Ag | Triaza-spiropiperidine derivatives for use as glyt-1 inhibitors in the treatment of neurological and neuropsychiatric disorders |
| GB0327380D0 (en) * | 2003-11-25 | 2003-12-31 | Cyclacel Ltd | Method |
| ITMI20040874A1 (it) | 2004-04-30 | 2004-07-30 | Ist Naz Stud Cura Dei Tumori | Derivati indolici ed azaindolici con azione antitumorale |
| EP1779848A1 (en) | 2005-10-28 | 2007-05-02 | Nikem Research S.R.L. | V-ATPase inhibitors for the treatment of inflammatory and autoimmune diseases |
| JO3235B1 (ar) * | 2006-05-26 | 2018-03-08 | Astex Therapeutics Ltd | مركبات بيررولوبيريميدين و استعمالاتها |
| ES2527696T3 (es) * | 2006-12-21 | 2015-01-28 | Nerviano Medical Sciences S.R.L. | Derivados de pirazoloquinazolina sustituidos, procedimientos para su preparación y su uso como inhibidores de la quinasa |
| CA2690748A1 (en) | 2007-06-25 | 2008-12-31 | Neurogen Corporation | Piperazinyl oxoalkyl tetrahydro-beta-carbolines and related analogues |
| EP2231656A1 (en) * | 2007-12-19 | 2010-09-29 | Amgen Inc. | Fused pyridine, pyrimidine and triazine compounds as cell cycle inhibitors |
| BRPI0917791B1 (pt) | 2008-08-22 | 2022-03-22 | Novartis Ag | Compostos de pirrolopirimidina como inibidores de cdk, bem como composição farmacêutica e combinação |
| CA2738909A1 (en) | 2008-10-01 | 2010-05-06 | The University Of North Carolina At Chapel Hill | Hematopoietic protection against ionizing radiation using selective cyclin-dependent kinase 4/6 inhibitors |
| CN102231984A (zh) | 2008-10-01 | 2011-11-02 | 北卡罗来纳大学查珀尔希尔分校 | 使用选择性细胞周期蛋白依赖性激酶4/6抑制剂对抗化疗化合物的造血防护 |
| EP3406260B1 (en) | 2009-05-13 | 2020-09-23 | The University of North Carolina at Chapel Hill | Cyclin dependent kinase inhibitors and methods of use |
| US9040519B2 (en) | 2010-02-18 | 2015-05-26 | Medivation Technologies, Inc. | Fused tetracyclic pyrido [4,3-B] indole and pyrido [3,4-B] indole derivatives and methods of use |
| CA2868966C (en) * | 2012-03-29 | 2021-01-26 | Francis Xavier Tavares | Lactam kinase inhibitors |
-
2011
- 2011-10-25 PL PL11838545.9T patent/PL2632467T3/pl unknown
- 2011-10-25 SG SG10201508715YA patent/SG10201508715YA/en unknown
- 2011-10-25 EP EP11838545.9A patent/EP2632467B1/en active Active
- 2011-10-25 DK DK11838545.9T patent/DK2632467T3/en active
- 2011-10-25 EP EP18167945.7A patent/EP3381920B1/en active Active
- 2011-10-25 MX MX2019010602A patent/MX379532B/es unknown
- 2011-10-25 BR BR112013010018-4A patent/BR112013010018B1/pt active IP Right Grant
- 2011-10-25 PT PT118385459T patent/PT2632467T/pt unknown
- 2011-10-25 MX MX2013004681A patent/MX338327B/es active IP Right Grant
- 2011-10-25 AU AU2011323739A patent/AU2011323739B2/en active Active
- 2011-10-25 ES ES11838545.9T patent/ES2592515T3/es active Active
- 2011-10-25 CA CA2961937A patent/CA2961937C/en active Active
- 2011-10-25 LT LTEP11838545.9T patent/LT2632467T/lt unknown
- 2011-10-25 EP EP21184036.8A patent/EP3981770A1/en not_active Withdrawn
- 2011-10-25 SI SI201130943A patent/SI2632467T1/sl unknown
- 2011-10-25 RU RU2013123790A patent/RU2621674C2/ru active
- 2011-10-25 CN CN201410184792.2A patent/CN103936745B/zh active Active
- 2011-10-25 MX MX2016004581A patent/MX367795B/es unknown
- 2011-10-25 EP EP19164126.5A patent/EP3567042B1/en active Active
- 2011-10-25 CN CN201180062297.9A patent/CN103429243B/zh active Active
- 2011-10-25 SG SG2013031554A patent/SG189525A1/en unknown
- 2011-10-25 KR KR1020137013388A patent/KR101929593B1/ko active Active
- 2011-10-25 EP EP16168485.7A patent/EP3118203B1/en active Active
- 2011-10-25 CN CN201610323241.9A patent/CN106008533B/zh active Active
- 2011-10-25 CN CN201611022263.8A patent/CN106967074A/zh active Pending
- 2011-10-25 CN CN201410184794.1A patent/CN104045654A/zh active Pending
- 2011-10-25 WO PCT/US2011/057749 patent/WO2012061156A1/en not_active Ceased
- 2011-10-25 JP JP2013535153A patent/JP5923509B2/ja active Active
- 2011-10-25 KR KR1020207034378A patent/KR20200137048A/ko not_active Ceased
- 2011-10-25 RS RS20160734A patent/RS55135B1/sr unknown
- 2011-10-25 EP EP15170738.7A patent/EP2955183A1/en not_active Withdrawn
- 2011-10-25 HR HRP20161092TT patent/HRP20161092T1/hr unknown
- 2011-10-25 KR KR1020197035200A patent/KR102186969B1/ko active Active
- 2011-10-25 KR KR1020187035510A patent/KR102051881B1/ko active Active
- 2011-10-25 MX MX2020005498A patent/MX385616B/es unknown
- 2011-10-25 CA CA2815084A patent/CA2815084C/en active Active
- 2011-10-25 HU HUE11838545A patent/HUE030714T2/en unknown
-
2013
- 2013-04-24 US US13/869,576 patent/US8598197B2/en active Active
- 2013-04-24 US US13/869,520 patent/US8598186B2/en active Active
- 2013-04-25 IL IL225940A patent/IL225940A0/en unknown
-
2014
- 2014-10-23 HK HK14110598.9A patent/HK1197067A1/xx unknown
-
2015
- 2015-03-05 IL IL237581A patent/IL237581B/en active IP Right Grant
- 2015-03-05 IL IL237582A patent/IL237582A0/en unknown
-
2016
- 2016-04-15 JP JP2016082206A patent/JP6157680B2/ja active Active
- 2016-07-13 AU AU2016204879A patent/AU2016204879B2/en active Active
- 2016-09-09 SM SM201600311T patent/SMT201600311B/it unknown
- 2016-09-13 CY CY20161100906T patent/CY1118004T1/el unknown
-
2017
- 2017-05-04 IL IL252108A patent/IL252108B/en active IP Right Grant
- 2017-06-02 JP JP2017110115A patent/JP6389926B2/ja active Active
-
2018
- 2018-04-30 AU AU2018202991A patent/AU2018202991B2/en active Active
- 2018-08-17 JP JP2018153563A patent/JP2018193400A/ja not_active Ceased
- 2018-10-18 HK HK18113421.2A patent/HK1254345B/en unknown
-
2020
- 2020-01-12 IL IL271977A patent/IL271977B/en active IP Right Grant
- 2020-05-07 AU AU2020203035A patent/AU2020203035B2/en active Active
- 2020-05-07 AU AU2020203037A patent/AU2020203037B2/en active Active
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| IL252108A0 (en) | cdk inhibitors | |
| GB201004179D0 (en) | Enzyme inhibitors | |
| GB2498145B (en) | Releasable corrosion inhibitors | |
| GB201004178D0 (en) | Enzyme inhibitors | |
| EP2552208A4 (en) | IMIDAZOLYL-IMIDAZOLES AS KINASE INHIBITORS | |
| EP2552214A4 (en) | PYRAZOLYL-PYRIMIDINES AS KINASE INHIBITORS | |
| PL2563771T3 (pl) | Związki inhibitora metaloenzymu | |
| EP2552211A4 (en) | INDAZOLYL-PYRIMIDINE AS KINASEHEMMER | |
| GB201004311D0 (en) | New enzyme inhibitor compounds | |
| GB201009731D0 (en) | Kinase inhibitors | |
| GB201016880D0 (en) | Phosphodiesterase inhibitors | |
| ZA201206456B (en) | Uses of dgati inhibitors | |
| GB201018996D0 (en) | Novel ROCK inhibitors | |
| ZA201303360B (en) | Kat ii inhibitors | |
| GB201009853D0 (en) | HSP90 inhibitors | |
| EP2521451A4 (en) | INHIBITORS OF THE HEDGEHOG PATH | |
| EP2632903A4 (en) | METALLOENZYMHEMMERVERBINDUNGEN | |
| GB201020798D0 (en) | Corrosion inhibitors | |
| GB201018480D0 (en) | Factors | |
| EP2651905A4 (en) | METALLOENZYMHEMMERVERBINDUNGEN | |
| ZA201303412B (en) | Kat ii inhibitors | |
| GB201018597D0 (en) | Inhibitors | |
| GB201004309D0 (en) | New enzyme inhibitors | |
| GB201003502D0 (en) | Novel inhibitors | |
| GB201006605D0 (en) | Novel inhibitors |