JP5923509B2 - Cdk阻害剤 - Google Patents
Cdk阻害剤 Download PDFInfo
- Publication number
- JP5923509B2 JP5923509B2 JP2013535153A JP2013535153A JP5923509B2 JP 5923509 B2 JP5923509 B2 JP 5923509B2 JP 2013535153 A JP2013535153 A JP 2013535153A JP 2013535153 A JP2013535153 A JP 2013535153A JP 5923509 B2 JP5923509 B2 JP 5923509B2
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- compound
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- butyl
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- methyl
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- 0 CN1CCN(*)CC1 Chemical compound CN1CCN(*)CC1 0.000 description 14
- RJXYGEQMLQMSOJ-PEHGTWAWSA-N CB(C1)N[C@@H](C)CN1C(C=C1)=CNC1N Chemical compound CB(C1)N[C@@H](C)CN1C(C=C1)=CNC1N RJXYGEQMLQMSOJ-PEHGTWAWSA-N 0.000 description 1
- OUKQMJJNYMRRHN-UHFFFAOYSA-N CC(C)(CN1)[n]2c3nc(Cl)ncc3cc2C1=O Chemical compound CC(C)(CN1)[n]2c3nc(Cl)ncc3cc2C1=O OUKQMJJNYMRRHN-UHFFFAOYSA-N 0.000 description 1
- CDCCIDIMKJJXEQ-UHFFFAOYSA-N CC(C)CC(CNC(OC(C)(C)C)=O)NC(OCc1ccccc1)=O Chemical compound CC(C)CC(CNC(OC(C)(C)C)=O)NC(OCc1ccccc1)=O CDCCIDIMKJJXEQ-UHFFFAOYSA-N 0.000 description 1
- QQHLFJUWYZZOOB-IBGZPJMESA-N CC(C)C[C@@H](CN1C)[n]2c3nc(Nc(cc4)ncc4N4CCN(C)CC4)ncc3cc2C1=O Chemical compound CC(C)C[C@@H](CN1C)[n]2c3nc(Nc(cc4)ncc4N4CCN(C)CC4)ncc3cc2C1=O QQHLFJUWYZZOOB-IBGZPJMESA-N 0.000 description 1
- QZDJLRICZNXNAT-SFHVURJKSA-N CC(C)C[C@@H](CN1C)[n]2c3nc(Nc(cc4)ncc4N4CCNCC4)ncc3cc2C1=O Chemical compound CC(C)C[C@@H](CN1C)[n]2c3nc(Nc(cc4)ncc4N4CCNCC4)ncc3cc2C1=O QZDJLRICZNXNAT-SFHVURJKSA-N 0.000 description 1
- JQBISHBIDUIUDU-KRWDZBQOSA-N CC(C)C[C@@H](CNC(c1c2)=O)[n]1c1c2cnc(Nc(cc2)ncc2N2CCNCC2)n1 Chemical compound CC(C)C[C@@H](CNC(c1c2)=O)[n]1c1c2cnc(Nc(cc2)ncc2N2CCNCC2)n1 JQBISHBIDUIUDU-KRWDZBQOSA-N 0.000 description 1
- JKNBNAZZNVQNBP-QGZVFWFLSA-N CC(C)[C@@H](CN1)[n]2c3nc(Nc(cc4)ncc4N4CCNCC4)ncc3cc2C1=O Chemical compound CC(C)[C@@H](CN1)[n]2c3nc(Nc(cc4)ncc4N4CCNCC4)ncc3cc2C1=O JKNBNAZZNVQNBP-QGZVFWFLSA-N 0.000 description 1
- IBFFTYPPDPEPLJ-UHFFFAOYSA-N CC(C1)NC(C)CN1c1ccc(Nc2ncc(cc3[n]4C5(CCCC5)CNC3=O)c4n2)nc1 Chemical compound CC(C1)NC(C)CN1c1ccc(Nc2ncc(cc3[n]4C5(CCCC5)CNC3=O)c4n2)nc1 IBFFTYPPDPEPLJ-UHFFFAOYSA-N 0.000 description 1
- HYQWMHHQUXUURL-XCWJXAQQSA-N CCC(C)[C@@H](CN1)[n]2c3nc(Nc(cc4)ncc4N4CCN(C)CC4)ncc3cc2C1=O Chemical compound CCC(C)[C@@H](CN1)[n]2c3nc(Nc(cc4)ncc4N4CCN(C)CC4)ncc3cc2C1=O HYQWMHHQUXUURL-XCWJXAQQSA-N 0.000 description 1
- HTLXTKMVRGTBQS-OTOKDRCRSA-N CCC(C)[C@@H](CN1C)[n]2c3nc(Nc(cc4)ncc4N4CCN(C)CC4)ncc3cc2C1=O Chemical compound CCC(C)[C@@H](CN1C)[n]2c3nc(Nc(cc4)ncc4N4CCN(C)CC4)ncc3cc2C1=O HTLXTKMVRGTBQS-OTOKDRCRSA-N 0.000 description 1
- YDOGEBDDNZDNJY-UHFFFAOYSA-N CN(CC1)CCN1S(C)(=O)=O Chemical compound CN(CC1)CCN1S(C)(=O)=O YDOGEBDDNZDNJY-UHFFFAOYSA-N 0.000 description 1
- PDGKHKMBHVFCMG-UHFFFAOYSA-N CN(CC1)CCN1c(cc1)cnc1Nc1ncc(cc2[n]3C4(CCCCC4)CNC2=O)c3n1 Chemical compound CN(CC1)CCN1c(cc1)cnc1Nc1ncc(cc2[n]3C4(CCCCC4)CNC2=O)c3n1 PDGKHKMBHVFCMG-UHFFFAOYSA-N 0.000 description 1
- YSRSYYHGSQMAFV-UHFFFAOYSA-N CN(CC12)CC1C2N Chemical compound CN(CC12)CC1C2N YSRSYYHGSQMAFV-UHFFFAOYSA-N 0.000 description 1
- PVOAHINGSUIXLS-UHFFFAOYSA-N CN1CCNCC1 Chemical compound CN1CCNCC1 PVOAHINGSUIXLS-UHFFFAOYSA-N 0.000 description 1
- PQDVKCXMZPIPAQ-UHFFFAOYSA-N O=C1NCC2(CCCC2)[n]2c3nc(Nc(cc4)ncc4N4CCSCC4)ncc3cc12 Chemical compound O=C1NCC2(CCCC2)[n]2c3nc(Nc(cc4)ncc4N4CCSCC4)ncc3cc12 PQDVKCXMZPIPAQ-UHFFFAOYSA-N 0.000 description 1
Images
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
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (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)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US40649810P | 2010-10-25 | 2010-10-25 | |
| US61/406,498 | 2010-10-25 | ||
| PCT/US2011/057749 WO2012061156A1 (en) | 2010-10-25 | 2011-10-25 | Cdk inhibitors |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016082206A Division JP6157680B2 (ja) | 2010-10-25 | 2016-04-15 | Cdk阻害剤 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013543845A JP2013543845A (ja) | 2013-12-09 |
| JP2013543845A5 JP2013543845A5 (https=) | 2014-12-18 |
| JP5923509B2 true JP5923509B2 (ja) | 2016-05-24 |
Family
ID=46024778
Family Applications (4)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013535153A Active JP5923509B2 (ja) | 2010-10-25 | 2011-10-25 | Cdk阻害剤 |
| JP2016082206A Active JP6157680B2 (ja) | 2010-10-25 | 2016-04-15 | Cdk阻害剤 |
| JP2017110115A Active JP6389926B2 (ja) | 2010-10-25 | 2017-06-02 | Cdk阻害剤 |
| JP2018153563A Ceased JP2018193400A (ja) | 2010-10-25 | 2018-08-17 | Cdk阻害剤 |
Family Applications After (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016082206A Active JP6157680B2 (ja) | 2010-10-25 | 2016-04-15 | Cdk阻害剤 |
| JP2017110115A Active JP6389926B2 (ja) | 2010-10-25 | 2017-06-02 | Cdk阻害剤 |
| JP2018153563A Ceased JP2018193400A (ja) | 2010-10-25 | 2018-08-17 | Cdk阻害剤 |
Country Status (25)
| Country | Link |
|---|---|
| US (2) | US8598186B2 (https=) |
| EP (6) | EP2632467B1 (https=) |
| JP (4) | JP5923509B2 (https=) |
| KR (4) | KR102051881B1 (https=) |
| CN (5) | CN106967074A (https=) |
| AU (5) | AU2011323739B2 (https=) |
| BR (1) | BR112013010018B1 (https=) |
| CA (2) | CA2961937C (https=) |
| CY (1) | CY1118004T1 (https=) |
| DK (1) | DK2632467T3 (https=) |
| ES (1) | ES2592515T3 (https=) |
| HK (2) | HK1197067A1 (https=) |
| HR (1) | HRP20161092T1 (https=) |
| HU (1) | HUE030714T2 (https=) |
| IL (5) | IL225940A0 (https=) |
| LT (1) | LT2632467T (https=) |
| MX (4) | MX338327B (https=) |
| PL (1) | PL2632467T3 (https=) |
| PT (1) | PT2632467T (https=) |
| RS (1) | RS55135B1 (https=) |
| RU (1) | RU2621674C2 (https=) |
| SG (2) | SG10201508715YA (https=) |
| SI (1) | SI2632467T1 (https=) |
| SM (1) | SMT201600311B (https=) |
| WO (1) | WO2012061156A1 (https=) |
Families Citing this family (133)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL1879573T3 (pl) | 2005-05-10 | 2013-05-31 | Incyte Holdings Corp | Modulatory 2,3-dioksygenazy indoloaminy i sposoby ich zastosowania |
| JP5465720B2 (ja) | 2008-07-08 | 2014-04-09 | インサイト・コーポレイション | インドールアミン2,3−ジオキシゲナーゼの阻害剤としての1,2,5−オキサジアゾール |
| JP2012526850A (ja) | 2009-05-13 | 2012-11-01 | ザ ユニバーシティ オブ ノース カロライナ アット チャペル ヒル | サイクリン依存性キナーゼ阻害剤及びその用法 |
| US8691830B2 (en) | 2010-10-25 | 2014-04-08 | G1 Therapeutics, Inc. | CDK inhibitors |
| WO2012068381A2 (en) | 2010-11-17 | 2012-05-24 | The University Of North Carolina At Chapel Hill | Protection of renal tissues from schema through inhibition of the proliferative kisses cdk4 and cdk6 |
| CA2868966C (en) | 2012-03-29 | 2021-01-26 | Francis Xavier Tavares | Lactam kinase inhibitors |
| CA2870019C (en) * | 2012-04-26 | 2020-08-18 | Francis Xavier Tavares | Synthesis of lactams |
| RS58514B1 (sr) | 2012-06-13 | 2019-04-30 | Incyte Holdings Corp | Supstituisana triciklična jedinjenja kao inhibitori fgfr |
| ME03557B (me) | 2013-03-15 | 2020-07-20 | G1 Therapeutics Inc | Privremena zaštiтa normalnih ćelija током hemoterapije |
| US20140274896A1 (en) * | 2013-03-15 | 2014-09-18 | G1 Therapeutics, Inc. | Transient Protection of Hematopoietic Stem and Progenitor Cells Against Ionizing Radiation |
| CA2906157C (en) * | 2013-03-15 | 2022-05-17 | G1 Therapeutics, Inc. | Highly active anti-neoplastic and anti-proliferative agents |
| PH12015502383B1 (en) | 2013-04-19 | 2023-02-03 | 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 |
| EP3191098A4 (en) | 2014-09-12 | 2018-04-25 | G1 Therapeutics, Inc. | Combinations and dosing regimes to treat rb-positive tumors |
| 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 |
| WO2016126889A1 (en) * | 2015-02-03 | 2016-08-11 | G1 Therapeutics, Inc. | Cdk4/6 inhibitor dosage formulations for the protection of hematopoietic stem and progenitor cells during chemotherapy |
| TWI712601B (zh) | 2015-02-20 | 2020-12-11 | 美商英塞特公司 | 作為fgfr抑制劑之雙環雜環 |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| WO2018005863A1 (en) * | 2016-07-01 | 2018-01-04 | G1 Therapeutics, Inc. | Pyrimidine-based compounds for the treatment of cancer |
| WO2018005533A1 (en) * | 2016-07-01 | 2018-01-04 | G1 Therapeutics, Inc. | Antiproliferative pyrimidine-based compounds |
| WO2018005865A1 (en) | 2016-07-01 | 2018-01-04 | G1 Therapeutics, Inc. | Synthesis of n-(heteroaryl)-pyrrolo[3,2-d]pyrimidin-2-amines |
| RU2019102647A (ru) * | 2016-07-01 | 2020-08-03 | Г1 Терапьютикс, Инк. | Антипролиферационные средства на основе пиримидина |
| BR112019003722A2 (pt) | 2016-08-23 | 2019-05-28 | Eisai R&D Man Co Ltd | terapias de combinação para o tratamento de carcinoma hepatocelular |
| US10849903B2 (en) | 2016-10-20 | 2020-12-01 | Pfizer Inc. | Anti-proliferative agents for treating PAH |
| US11865176B2 (en) | 2016-11-08 | 2024-01-09 | Dana-Farber Cancer Institute, Inc. | Compositions and methods of modulating anti-tumor immunity |
| EP3505519B1 (en) * | 2016-11-11 | 2022-01-05 | Shanghai Haiyan Pharmaceutical Technology Co., Ltd. | Pyridinamine-substituted heterotricyclo compounds, preparation thereof, and use in medicines |
| KR20190092478A (ko) | 2016-12-05 | 2019-08-07 | 쥐원 쎄라퓨틱스, 인크. | 화학요법 레지멘 동안의 면역 반응의 보존 |
| MX2019008158A (es) | 2017-01-06 | 2019-12-09 | G1 Therapeutics Inc | Terapia de combinacion para el tratamiento del cancer. |
| US11395821B2 (en) | 2017-01-30 | 2022-07-26 | G1 Therapeutics, Inc. | Treatment of EGFR-driven cancer with fewer side effects |
| EP3585389A4 (en) | 2017-02-22 | 2020-12-23 | G1 Therapeutics, Inc. | EGFR-CAUSED CANCER TREATMENT WITH LESS SIDE EFFECTS |
| MX2019010981A (es) | 2017-03-16 | 2020-09-07 | Eisai R&D Man Co Ltd | Terapias de combinacion para el tratamiento de cancer de mama. |
| AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
| WO2019006393A1 (en) | 2017-06-29 | 2019-01-03 | G1 Therapeutics, Inc. | Morphic forms of git38 and methods of manufacture thereof |
| 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 |
| EP3738084A4 (en) | 2018-01-08 | 2021-11-17 | G1 Therapeutics, Inc. | SUPERIOR G1T38 DOSING SCHEMES |
| TWI877770B (zh) | 2018-02-27 | 2025-03-21 | 美商英塞特公司 | 作為a2a / a2b抑制劑之咪唑并嘧啶及三唑并嘧啶 |
| HRP20241288T1 (hr) | 2018-05-04 | 2024-12-06 | Incyte Corporation | Čvrsti oblici fgfr inhibitora i postupci za njihovu proizvodnju |
| AU2019262579B2 (en) | 2018-05-04 | 2024-09-12 | Incyte Corporation | Salts of an FGFR inhibitor |
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| AU2019325685B2 (en) | 2018-08-24 | 2025-07-24 | Pharmacosmos Holding A/S | Improved synthesis of 1,4-diazaspiro(5.5)undecan-3-one |
| EP3849537B1 (en) | 2018-09-10 | 2024-10-23 | 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 |
| US20220040324A1 (en) | 2018-12-21 | 2022-02-10 | 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 |
| 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 |
| PH12021551976A1 (en) | 2019-02-15 | 2022-07-04 | Incyte Corp | Cyclin-dependent kinase 2 biomarkers and uses thereof |
| 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 |
| US11628162B2 (en) | 2019-03-08 | 2023-04-18 | 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 |
| US11447494B2 (en) | 2019-05-01 | 2022-09-20 | Incyte Corporation | Tricyclic amine compounds as CDK2 inhibitors |
| WO2020223469A1 (en) | 2019-05-01 | 2020-11-05 | Incyte Corporation | N-(1-(methylsulfonyl)piperidin-4-yl)-4,5-di hydro-1h-imidazo[4,5-h]quinazolin-8-amine derivatives and related compounds as cyclin-dependent kinase 2 (cdk2) inhibitors for treating cancer |
| TW202114684A (zh) | 2019-06-18 | 2021-04-16 | 美商G1治療公司 | 增強癌症病患之抗腫瘤免疫之方法 |
| US11591329B2 (en) | 2019-07-09 | 2023-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| KR20220044527A (ko) | 2019-08-01 | 2022-04-08 | 인사이트 코포레이션 | Ido 억제제의 투여 요법 |
| CA3150681A1 (en) | 2019-08-14 | 2021-02-18 | Incyte Corporation | Imidazolyl pyrimidinylamine compounds as cdk2 inhibitors |
| WO2021067374A1 (en) | 2019-10-01 | 2021-04-08 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| US11851426B2 (en) | 2019-10-11 | 2023-12-26 | Incyte Corporation | Bicyclic amines as CDK2 inhibitors |
| CA3157361A1 (en) | 2019-10-14 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
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