KR100904570B1 - 종양성 질환, 염증성 및 면역계 장애의 치료에 유용한2,4-피리미딘디아민 - Google Patents
종양성 질환, 염증성 및 면역계 장애의 치료에 유용한2,4-피리미딘디아민 Download PDFInfo
- Publication number
- KR100904570B1 KR100904570B1 KR1020067003056A KR20067003056A KR100904570B1 KR 100904570 B1 KR100904570 B1 KR 100904570B1 KR 1020067003056 A KR1020067003056 A KR 1020067003056A KR 20067003056 A KR20067003056 A KR 20067003056A KR 100904570 B1 KR100904570 B1 KR 100904570B1
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- South Korea
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- alkyl
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- unsubstituted
- alkoxy
- methyl
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- 0 CNS(c1ccccc1Nc(nc(N*)nc1)c1Br)(=O)=O Chemical compound CNS(c1ccccc1Nc(nc(N*)nc1)c1Br)(=O)=O 0.000 description 3
- ANQMORUIOZZXOR-UHFFFAOYSA-N CC(CC=C1CN2C)C(Nc3nc(Nc(c(OC)c4)ccc4N4CCOCC4)ncc3Cl)=C1C2=O Chemical compound CC(CC=C1CN2C)C(Nc3nc(Nc(c(OC)c4)ccc4N4CCOCC4)ncc3Cl)=C1C2=O ANQMORUIOZZXOR-UHFFFAOYSA-N 0.000 description 1
- ZYCXAGUCFFRHHW-UHFFFAOYSA-N CC(N(CC1)CCN1c(cc1)cc([NH+]([O-])[O-])c1OC)=O Chemical compound CC(N(CC1)CCN1c(cc1)cc([NH+]([O-])[O-])c1OC)=O ZYCXAGUCFFRHHW-UHFFFAOYSA-N 0.000 description 1
- XXHKCOWKQMQGET-UHFFFAOYSA-N CCC(C(C)c1cccc(Nc(nc(Nc(ccc(N(CC2)CCC2N2CCCCC2)c2)c2OC)nc2)c2Cl)c1S(=O)=O)N Chemical compound CCC(C(C)c1cccc(Nc(nc(Nc(ccc(N(CC2)CCC2N2CCCCC2)c2)c2OC)nc2)c2Cl)c1S(=O)=O)N XXHKCOWKQMQGET-UHFFFAOYSA-N 0.000 description 1
- GQVZXZORIINEQF-UHFFFAOYSA-N CCC(CC)NS(c(cccc1)c1Nc(nc(Nc(ccc(OC1CN(CC)CC1)c1)c1OCC)nc1)c1Cl)(=O)=O Chemical compound CCC(CC)NS(c(cccc1)c1Nc(nc(Nc(ccc(OC1CN(CC)CC1)c1)c1OCC)nc1)c1Cl)(=O)=O GQVZXZORIINEQF-UHFFFAOYSA-N 0.000 description 1
- UOUMNCDDFNFBNG-HXUWFJFHSA-N CCC(CC)NS(c(cccc1)c1Nc1nc(Nc(c(OC)c2)ccc2O[C@H]2CN(C)CC2)ncc1Cl)(=O)=O Chemical compound CCC(CC)NS(c(cccc1)c1Nc1nc(Nc(c(OC)c2)ccc2O[C@H]2CN(C)CC2)ncc1Cl)(=O)=O UOUMNCDDFNFBNG-HXUWFJFHSA-N 0.000 description 1
- YOYCVJKZYMLVQC-NRFANRHFSA-N CCC(CC)NS(c(cccc1)c1Nc1nc(Nc(c(OCC)c2)ccc2O[C@@H]2CN(C)CC2)ncc1Cl)(=O)=O Chemical compound CCC(CC)NS(c(cccc1)c1Nc1nc(Nc(c(OCC)c2)ccc2O[C@@H]2CN(C)CC2)ncc1Cl)(=O)=O YOYCVJKZYMLVQC-NRFANRHFSA-N 0.000 description 1
- YOYCVJKZYMLVQC-OAQYLSRUSA-N CCC(CC)NS(c(cccc1)c1Nc1nc(Nc(c(OCC)c2)ccc2O[C@H]2CN(C)CC2)ncc1Cl)(=O)=O Chemical compound CCC(CC)NS(c(cccc1)c1Nc1nc(Nc(c(OCC)c2)ccc2O[C@H]2CN(C)CC2)ncc1Cl)(=O)=O YOYCVJKZYMLVQC-OAQYLSRUSA-N 0.000 description 1
- NISHILSJOFWGEW-UHFFFAOYSA-N CCN(CC1)CC1Oc(cc1)cc(OCC)c1Nc(nc1)nc(NC2C=CC=CC2S(CNCC(C)C)(=O)=O)c1Br Chemical compound CCN(CC1)CC1Oc(cc1)cc(OCC)c1Nc(nc1)nc(NC2C=CC=CC2S(CNCC(C)C)(=O)=O)c1Br NISHILSJOFWGEW-UHFFFAOYSA-N 0.000 description 1
- BPUCHTKTPGFFHN-UHFFFAOYSA-N CCN(CC1)CCN1c(cc1OCC)ccc1Nc(nc1Nc(cccc2)c2S(NC)(=O)=O)ncc1Br Chemical compound CCN(CC1)CCN1c(cc1OCC)ccc1Nc(nc1Nc(cccc2)c2S(NC)(=O)=O)ncc1Br BPUCHTKTPGFFHN-UHFFFAOYSA-N 0.000 description 1
- GVDMSADBJPPLJD-UHFFFAOYSA-N CCN(CC1)CCN1c(cc1OCC)ccc1Nc(nc1Nc(cccc2)c2S(NC)(=O)=O)ncc1Cl Chemical compound CCN(CC1)CCN1c(cc1OCC)ccc1Nc(nc1Nc(cccc2)c2S(NC)(=O)=O)ncc1Cl GVDMSADBJPPLJD-UHFFFAOYSA-N 0.000 description 1
- JKZAUJMXKHOGGC-UHFFFAOYSA-N CCOc1cc(N2CCN(C)CC2)ccc1Nc(nc1Nc(cccc2)c2S(NC)(=O)=O)ncc1Br Chemical compound CCOc1cc(N2CCN(C)CC2)ccc1Nc(nc1Nc(cccc2)c2S(NC)(=O)=O)ncc1Br JKZAUJMXKHOGGC-UHFFFAOYSA-N 0.000 description 1
- VYGDZXFAMXGDBM-UHFFFAOYSA-N CCOc1cc(N2CCN(C)CC2)ccc1Nc(nc1Nc(cccc2)c2S(NC)(=O)=O)ncc1Cl Chemical compound CCOc1cc(N2CCN(C)CC2)ccc1Nc(nc1Nc(cccc2)c2S(NC)(=O)=O)ncc1Cl VYGDZXFAMXGDBM-UHFFFAOYSA-N 0.000 description 1
- XWZDGGDSFVKQGT-IBGZPJMESA-N CCOc1cc(O[C@@H]2CN(C)CC2)ccc1Nc(nc1Nc(cccc2)c2S(NC(C)C)(=O)=O)ncc1Cl Chemical compound CCOc1cc(O[C@@H]2CN(C)CC2)ccc1Nc(nc1Nc(cccc2)c2S(NC(C)C)(=O)=O)ncc1Cl XWZDGGDSFVKQGT-IBGZPJMESA-N 0.000 description 1
- NLGVFVMNYZVFJK-NRFANRHFSA-N CCOc1cc(O[C@@H]2CN(C)CC2)ccc1Nc(nc1Nc(cccc2)c2S(NC2CCCC2)(=O)=O)ncc1Cl Chemical compound CCOc1cc(O[C@@H]2CN(C)CC2)ccc1Nc(nc1Nc(cccc2)c2S(NC2CCCC2)(=O)=O)ncc1Cl NLGVFVMNYZVFJK-NRFANRHFSA-N 0.000 description 1
- HEGUQXXJZHJSGI-HXUWFJFHSA-N CCOc1cc(O[C@H](CC2)CN2I)ccc1Nc(nc1Nc(cccc2)c2S(NC2CCCC2)(=O)=O)ncc1Cl Chemical compound CCOc1cc(O[C@H](CC2)CN2I)ccc1Nc(nc1Nc(cccc2)c2S(NC2CCCC2)(=O)=O)ncc1Cl HEGUQXXJZHJSGI-HXUWFJFHSA-N 0.000 description 1
- YKPATXXNIXWMNF-UHFFFAOYSA-N CN(C)S(c(cccc1)c1Nc1nc(Nc(c(OC)c2)ccc2C(N2CCOCC2)=O)ncc1Cl)(=O)=O Chemical compound CN(C)S(c(cccc1)c1Nc1nc(Nc(c(OC)c2)ccc2C(N2CCOCC2)=O)ncc1Cl)(=O)=O YKPATXXNIXWMNF-UHFFFAOYSA-N 0.000 description 1
- PPBYTGQGFVYLFZ-INIZCTEOSA-N CN(C)S(c(cccc1)c1Nc1nc(Nc(c(OC)c2)ccc2O[C@@H](CC2)CN2I)ncc1Cl)(=O)=O Chemical compound CN(C)S(c(cccc1)c1Nc1nc(Nc(c(OC)c2)ccc2O[C@@H](CC2)CN2I)ncc1Cl)(=O)=O PPBYTGQGFVYLFZ-INIZCTEOSA-N 0.000 description 1
- IQOVKKNJOSUWBS-FQEVSTJZSA-N CN(CC1)C[C@H]1Oc(cc1OC)ccc1Nc(nc1Nc(cccc2)c2S(C2CCCCC2)(=O)=O)ncc1Cl Chemical compound CN(CC1)C[C@H]1Oc(cc1OC)ccc1Nc(nc1Nc(cccc2)c2S(C2CCCCC2)(=O)=O)ncc1Cl IQOVKKNJOSUWBS-FQEVSTJZSA-N 0.000 description 1
- JVXVCEFIYQQHJR-FQEVSTJZSA-N CN(CC1)C[C@H]1Oc(cc1OC)ccc1Nc(nc1Nc(cccc2)c2S(NC2CCCC2)(=O)=O)ncc1Cl Chemical compound CN(CC1)C[C@H]1Oc(cc1OC)ccc1Nc(nc1Nc(cccc2)c2S(NC2CCCC2)(=O)=O)ncc1Cl JVXVCEFIYQQHJR-FQEVSTJZSA-N 0.000 description 1
- MDAHROZOBPNKFR-UHFFFAOYSA-N CNCCc1ccccc1Nc(nc(Nc(ccc(N(CC1)CCC1N1CCCCC1)c1)c1OC)nc1)c1Br Chemical compound CNCCc1ccccc1Nc(nc(Nc(ccc(N(CC1)CCC1N1CCCCC1)c1)c1OC)nc1)c1Br MDAHROZOBPNKFR-UHFFFAOYSA-N 0.000 description 1
- RVNZVWJCTGZHIF-UHFFFAOYSA-N CNS(c(cccc1)c1Nc1nc(Nc(c(OC)c2)ccc2C(N(CC2)CCC2N2CCCCC2)=O)ncc1Br)(=O)=O Chemical compound CNS(c(cccc1)c1Nc1nc(Nc(c(OC)c2)ccc2C(N(CC2)CCC2N2CCCCC2)=O)ncc1Br)(=O)=O RVNZVWJCTGZHIF-UHFFFAOYSA-N 0.000 description 1
- CTPIWWBBOZVNCS-UHFFFAOYSA-N CNS(c(cccc1)c1Nc1nc(Nc(c(OCC2CC2)c2)ccc2N(CC2)CCC2N2CCCCC2)ncc1Cl)(=O)=O Chemical compound CNS(c(cccc1)c1Nc1nc(Nc(c(OCC2CC2)c2)ccc2N(CC2)CCC2N2CCCCC2)ncc1Cl)(=O)=O CTPIWWBBOZVNCS-UHFFFAOYSA-N 0.000 description 1
- DHSXYOWXKKKABN-UHFFFAOYSA-N CNS(c(cccc1)c1Nc1nc(Nc(c(OCC2CC2)c2)ccc2N(CC2)CCC2N2CCOCC2)ncc1Br)(=O)=O Chemical compound CNS(c(cccc1)c1Nc1nc(Nc(c(OCC2CC2)c2)ccc2N(CC2)CCC2N2CCOCC2)ncc1Br)(=O)=O DHSXYOWXKKKABN-UHFFFAOYSA-N 0.000 description 1
- VDOQEOVKPMZKJA-UHFFFAOYSA-N CNS(c1c(CCCc(nc(nc2)Cl)c2[N+](C)([O-])O)cccc1)(=O)=O Chemical compound CNS(c1c(CCCc(nc(nc2)Cl)c2[N+](C)([O-])O)cccc1)(=O)=O VDOQEOVKPMZKJA-UHFFFAOYSA-N 0.000 description 1
- HCPLJTFWHJREKI-UHFFFAOYSA-N CNS(c1ccccc1Nc(nc(nc1)Cl)c1Br)(=O)=O Chemical compound CNS(c1ccccc1Nc(nc(nc1)Cl)c1Br)(=O)=O HCPLJTFWHJREKI-UHFFFAOYSA-N 0.000 description 1
- UAJKCDSLLCLCEO-UHFFFAOYSA-N COc(cc(cc1)N(CC2)CCC2N2CCCCC2)c1Nc(nc1)nc(Nc2c(CCNC3CCCC3)cccc2)c1Cl Chemical compound COc(cc(cc1)N(CC2)CCC2N2CCCCC2)c1Nc(nc1)nc(Nc2c(CCNC3CCCC3)cccc2)c1Cl UAJKCDSLLCLCEO-UHFFFAOYSA-N 0.000 description 1
- PKEYIJHNHAONDX-LJQANCHMSA-N COc1cc(O[C@H](CC2)CN2I)ccc1Nc(nc1Nc(cccc2)c2S(C2CCCCC2)(=O)=O)ncc1Cl Chemical compound COc1cc(O[C@H](CC2)CN2I)ccc1Nc(nc1Nc(cccc2)c2S(C2CCCCC2)(=O)=O)ncc1Cl PKEYIJHNHAONDX-LJQANCHMSA-N 0.000 description 1
- UBTIIZMTNHCGND-UHFFFAOYSA-N Cc(c([N+](O)=O)c1)ccc1-c(cc1)ccc1OC Chemical compound Cc(c([N+](O)=O)c1)ccc1-c(cc1)ccc1OC UBTIIZMTNHCGND-UHFFFAOYSA-N 0.000 description 1
- BAGAORHMZVFECP-UHFFFAOYSA-N Cc1cc(N2CCOCC2)ccc1Nc(nc1NN)ncc1Cl Chemical compound Cc1cc(N2CCOCC2)ccc1Nc(nc1NN)ncc1Cl BAGAORHMZVFECP-UHFFFAOYSA-N 0.000 description 1
- TXJUTRJFNRYTHH-UHFFFAOYSA-N O=C(c(cccc1)c1N1)OC1=O Chemical compound O=C(c(cccc1)c1N1)OC1=O TXJUTRJFNRYTHH-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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| GB0322370A GB0322370D0 (en) | 2003-09-24 | 2003-09-24 | Organic compounds |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013176503A1 (ko) | 2012-05-24 | 2013-11-28 | 서울대학교 산학협력단 | 타우 단백질 매개 신경 퇴행성 질환 치료제 |
| WO2014025128A1 (ko) * | 2012-08-10 | 2014-02-13 | 한국화학연구원 | N2,n4-비스(4-(피페라진-1-일)페닐)피리미딘-2,4-디아민 유도체 또는 이의 약학적으로 허용 가능한 염 및 이를 유효성분으로 함유하는 암의 예방 또는 치료용 약학적 조성물 |
Families Citing this family (206)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI329105B (en) | 2002-02-01 | 2010-08-21 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds and their uses |
| GB0206215D0 (en) * | 2002-03-15 | 2002-05-01 | Novartis Ag | Organic compounds |
| ATE451104T1 (de) | 2002-07-29 | 2009-12-15 | Rigel Pharmaceuticals Inc | Verfahren zur behandlung oder pruvention von autoimmunkrankheiten mit 2,4-pyrimidindiamin- verbindungen |
| DE602004009295T2 (de) | 2003-01-14 | 2008-07-03 | Arena Pharmaceuticals, Inc., San Diego | 1,2,3-trisubstituierte aryl- und heteroarylderivate als modulatoren des metabolismus zur vorbeugung und behandlung von metabolismus-bedingten krankheiten wie diabetes oder hyperglykämie |
| GB0305929D0 (en) | 2003-03-14 | 2003-04-23 | Novartis Ag | Organic compounds |
| JP2004313181A (ja) * | 2003-04-02 | 2004-11-11 | Canon Inc | 感染症起炎菌検出用プローブ及びプローブセット、ならびに担体及び遺伝子検査方法 |
| AR045047A1 (es) | 2003-07-11 | 2005-10-12 | Arena Pharm Inc | Derivados arilo y heteroarilo trisustituidos como moduladores del metabolismo y de la profilaxis y tratamiento de desordenes relacionados con los mismos |
| ES2421139T3 (es) | 2003-07-30 | 2013-08-29 | Rigel Pharmaceuticals, Inc. | Compuestos de 2,4-pirimidindiamina para su uso en el tratamiento o la prevención de enfermedades autoinmunitarias |
| DK2287156T3 (da) * | 2003-08-15 | 2013-08-26 | Novartis Ag | 2,4-Di(phenylamino)-pyrimidiner egnede i behandling af neoplastiske sygdomme, inflammatoriske lidelser og lidelser i immunsystemet |
| US8131475B2 (en) | 2003-09-03 | 2012-03-06 | The United States Of America As Represented By The Secretary, Department Of Health And Human Services | Methods for identifying, diagnosing, and predicting survival of lymphomas |
| US7456176B2 (en) | 2004-04-08 | 2008-11-25 | Targegen, Inc. | Benzotriazine inhibitors of kinases |
| EP1598343A1 (de) * | 2004-05-19 | 2005-11-23 | Boehringer Ingelheim International GmbH | 2-Arylaminopyrimidine als PLK Inhibitoren |
| US7521457B2 (en) * | 2004-08-20 | 2009-04-21 | Boehringer Ingelheim International Gmbh | Pyrimidines as PLK inhibitors |
| US7652051B2 (en) | 2004-08-25 | 2010-01-26 | Targegen, Inc. | Heterocyclic compounds and methods of use |
| GB0419161D0 (en) * | 2004-08-27 | 2004-09-29 | Novartis Ag | Organic compounds |
| EP2161275A1 (en) | 2005-01-19 | 2010-03-10 | Rigel Pharmaceuticals, Inc. | Prodrugs of 2,4-pyrimidinediamine compounds and their uses |
| US20070203161A1 (en) | 2006-02-24 | 2007-08-30 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the jak pathway |
| US7491732B2 (en) | 2005-06-08 | 2009-02-17 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the JAK pathway |
| AR054834A1 (es) * | 2005-07-15 | 2007-07-18 | Glaxo Group Ltd | Derivados de 1,1-dioxido-2,3-dihidro-1,2-benzoisotiazol-6-il-1h-indazol-4-il-2,4 pirimidina diamina |
| WO2007028445A1 (en) * | 2005-07-15 | 2007-03-15 | Glaxo Group Limited | 6-indolyl-4-yl-amino-5-halogeno-2-pyrimidinyl-amino derivatives |
| GB0517329D0 (en) * | 2005-08-25 | 2005-10-05 | Merck Sharp & Dohme | Stimulation of neurogenesis |
| US8604042B2 (en) | 2005-11-01 | 2013-12-10 | Targegen, Inc. | Bi-aryl meta-pyrimidine inhibitors of kinases |
| US8133900B2 (en) | 2005-11-01 | 2012-03-13 | Targegen, Inc. | Use of bi-aryl meta-pyrimidine inhibitors of kinases |
| NZ592990A (en) | 2005-11-01 | 2013-01-25 | Targegen Inc | Bi-aryl meta-pyrimidine inhibitors of kinases |
| TW200736232A (en) * | 2006-01-26 | 2007-10-01 | Astrazeneca Ab | Pyrimidine derivatives |
| WO2007085540A1 (en) * | 2006-01-27 | 2007-08-02 | Glaxo Group Limited | 1h-indaz0l-4-yl-2 , 4-pyrimidinediamine derivatives |
| US7659280B2 (en) | 2006-02-17 | 2010-02-09 | Rigel Pharmaceuticals, Inc. | 2,4-pyrimidinediamine compounds for treating or preventing autoimmune diseases |
| WO2007098507A2 (en) | 2006-02-24 | 2007-08-30 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the jak pathway |
| US7700339B2 (en) | 2006-04-14 | 2010-04-20 | Cell Signaling Technology, Inc. | Gene defects and mutant ALK kinase in human solid tumors |
| US8168383B2 (en) | 2006-04-14 | 2012-05-01 | Cell Signaling Technology, Inc. | Gene defects and mutant ALK kinase in human solid tumors |
| EP1914240B1 (en) | 2006-10-11 | 2009-12-02 | Astellas Pharma Inc. | EML4-ALK fusion gene |
| CA2598893C (en) | 2006-10-11 | 2012-04-10 | Astellas Pharma Inc. | Eml4-alk fusion gene |
| AU2007309427B2 (en) | 2006-10-23 | 2013-02-28 | Cephalon, Inc. | Fused bicyclic derivatives of 2,4-diaminopyrimidine as ALK and c-Met inhibitors |
| KR101149295B1 (ko) * | 2006-12-08 | 2012-07-05 | 아이알엠 엘엘씨 | 단백질 키나제 억제제로서의 화합물 |
| RS53588B1 (sr) * | 2006-12-08 | 2015-02-27 | Irm Llc | Jedinjenja i kompozicije kao inhibitori protein kinaza |
| CA2670645A1 (en) * | 2006-12-19 | 2008-07-03 | Genentech, Inc. | Pyrimidine kinase inhibitors |
| AR065015A1 (es) | 2007-01-26 | 2009-05-13 | Smithkline Beecham Corp | Derivados de antranilamida, composiciones farmaceuticas que los contienen, y usos para el tratamiento del cancer |
| WO2008129380A1 (en) | 2007-04-18 | 2008-10-30 | Pfizer Products Inc. | Sulfonyl amide derivatives for the treatment of abnormal cell growth |
| TWI389893B (zh) * | 2007-07-06 | 2013-03-21 | Astellas Pharma Inc | 二(芳胺基)芳基化合物 |
| CN101796046A (zh) | 2007-07-16 | 2010-08-04 | 阿斯利康(瑞典)有限公司 | 嘧啶衍生物934 |
| CN101827848B (zh) | 2007-08-08 | 2012-11-07 | 葛兰素史密丝克莱恩有限责任公司 | 作为IGF-1R抑制剂用于治疗癌症的2-[(2-{苯基氨基}-1H-吡咯并[2,3-d]嘧啶-4-基)氨基]苯甲酰胺衍生物 |
| CA2696824A1 (en) | 2007-08-28 | 2009-03-12 | Irm Llc | Compounds and compositions as kinase inhibitors |
| WO2009032703A1 (en) * | 2007-08-28 | 2009-03-12 | Irm Llc | 2- (het) arylamino-6-aminopyridine derivatives and fused forms thereof as anaplastic lymphoma kinase inhibitors |
| CA2710118A1 (en) | 2007-12-20 | 2009-07-02 | Cellzome Limited | Sulfamides as zap-70 inhibitors |
| WO2009105498A1 (en) * | 2008-02-19 | 2009-08-27 | Smithkline Beecham Corporation | Anilinopyridines as inhibitors of fak |
| JP5298187B2 (ja) * | 2008-04-07 | 2013-09-25 | アイアールエム・リミテッド・ライアビリティ・カンパニー | タンパク質キナーゼ阻害剤としての化合物および組成物 |
| US8138339B2 (en) | 2008-04-16 | 2012-03-20 | Portola Pharmaceuticals, Inc. | Inhibitors of protein kinases |
| CN102066339B (zh) | 2008-04-16 | 2014-09-24 | 波托拉医药品公司 | 作为syk或jak蛋白激酶抑制剂的2,6-二氨基-嘧啶-5-基甲酰胺类化合物 |
| NZ589315A (en) | 2008-04-16 | 2012-11-30 | Portola Pharm Inc | 2,6-diamino-pyrimidin-5-yl-carboxamides as Spleen tryosine kinase (syk) or Janus kinase (JAK) inhibitors |
| NZ588830A (en) | 2008-04-22 | 2012-11-30 | Portola Pharm Inc | Inhibitors of protein kinases |
| PL2300013T5 (pl) * | 2008-05-21 | 2025-04-28 | Takeda Pharmaceutical Company Limited | Pochodne fosforu jako inhibitor kinazy |
| US9273077B2 (en) | 2008-05-21 | 2016-03-01 | Ariad Pharmaceuticals, Inc. | Phosphorus derivatives as kinase inhibitors |
| MX2010014057A (es) * | 2008-06-17 | 2011-03-21 | Astrazeneca Ab | Compuestos de piridina. |
| UY31929A (es) | 2008-06-25 | 2010-01-05 | Irm Llc | Compuestos y composiciones como inhibidores de cinasa |
| US8445505B2 (en) | 2008-06-25 | 2013-05-21 | Irm Llc | Pyrimidine derivatives as kinase inhibitors |
| US8338439B2 (en) | 2008-06-27 | 2012-12-25 | Celgene Avilomics Research, Inc. | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
| TWI458721B (zh) | 2008-06-27 | 2014-11-01 | Celgene Avilomics Res Inc | 雜芳基化合物及其用途 |
| US11351168B1 (en) | 2008-06-27 | 2022-06-07 | Celgene Car Llc | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
| JO3067B1 (ar) * | 2008-10-27 | 2017-03-15 | Glaxosmithkline Llc | بيرميدينات بيرازولو امينو كمثبطات ل fak |
| TW201024281A (en) | 2008-11-24 | 2010-07-01 | Boehringer Ingelheim Int | New compounds |
| AR074210A1 (es) | 2008-11-24 | 2010-12-29 | Boehringer Ingelheim Int | Derivados de pirimidina como inhibidores de ptk2-quinasa |
| AR074830A1 (es) | 2008-12-19 | 2011-02-16 | Cephalon Inc | Pirrolotriazinas como inhibidores de alk y jak2 |
| SG2014005318A (en) | 2009-01-23 | 2014-03-28 | Rigel Pharmaceuticals Inc | Compositions and methods for inhibition of the jak pathway |
| WO2010112210A1 (en) | 2009-04-03 | 2010-10-07 | Cellzome Ag | Methods for the identification of kinase interacting molecules and for the purification of kinase proteins |
| EP2419423A1 (en) | 2009-04-14 | 2012-02-22 | Cellzome Limited | Fluoro substituted pyrimidine compounds as jak3 inhibitors |
| KR101705158B1 (ko) | 2009-05-05 | 2017-02-09 | 다나-파버 캔서 인스티튜트 인크. | Egfr 억제제 및 질환 치료방법 |
| TW201100441A (en) | 2009-06-01 | 2011-01-01 | Osi Pharm Inc | Amino pyrimidine anticancer compounds |
| MX2011013325A (es) * | 2009-06-10 | 2012-04-30 | Abbott Lab | 2-(lh-pirazol-4-ilamino)-pirimidina como inhibidores de cinasa. |
| US20120142667A1 (en) * | 2009-06-10 | 2012-06-07 | Nigel Ramsden | Pyrimidine derivatives as zap-70 inhibitors |
| CN102480966B (zh) | 2009-06-12 | 2015-09-16 | 达娜-法勃肿瘤研究所公司 | 融合的杂环化合物及其用途 |
| CA2763730A1 (en) * | 2009-06-18 | 2010-12-23 | Cellzome Limited | Heterocyclylaminopyrimidines as kinase inhibitors |
| CA2763720A1 (en) * | 2009-06-18 | 2010-12-23 | Cellzome Limited | Sulfonamides and sulfamides as zap-70 inhibitors |
| US20120172385A1 (en) * | 2009-09-11 | 2012-07-05 | Richard John Harrison | Ortho substituted pyrimidine compounds as jak inhibitors |
| WO2011140338A1 (en) * | 2010-05-05 | 2011-11-10 | Gatekeeper Pharmaceuticals, Inc. | Compounds that modulate egfr activity and methods for treating or preventing conditions therewith |
| JP5607241B2 (ja) | 2010-05-21 | 2014-10-15 | ケミリア・エービー | 新規ピリミジン誘導体 |
| WO2012019132A2 (en) | 2010-08-06 | 2012-02-09 | Cell Signaling Technology, Inc. | Anaplastic lymphoma kinase in kidney cancer |
| RU2013109393A (ru) | 2010-08-10 | 2014-09-20 | Сэлджин Авиаломикс Ресеарч, Инк. | Безилатная соль ингибитора втк |
| PH12013500547A1 (en) | 2010-09-22 | 2013-06-10 | Arena Pharm Inc | Modulators of the gpr119 receptor and the treatment of disorders related thereto |
| EP2635556B1 (en) | 2010-11-01 | 2017-06-21 | Portola Pharmaceuticals, Inc. | Benzamides and nicotinamides as syk modulators |
| US9102625B2 (en) | 2010-11-01 | 2015-08-11 | Portola Pharmaceuticals, Inc. | Nicotinamides as JAK kinase modulators |
| US20130317029A1 (en) | 2010-11-01 | 2013-11-28 | Portola Pharmaceuticals, Inc. | Oxypyrimidines as syk modulators |
| EP2635285B1 (en) | 2010-11-01 | 2017-05-03 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
| CA2815858C (en) | 2010-11-01 | 2018-10-16 | Celgene Avilomics Research, Inc. | Heterocyclic compounds and uses thereof |
| WO2012060847A1 (en) | 2010-11-07 | 2012-05-10 | Targegen, Inc. | Compositions and methods for treating myelofibrosis |
| EP2637502B1 (en) | 2010-11-10 | 2018-01-10 | Celgene CAR LLC | Mutant-selective egfr inhibitors and uses thereof |
| PL2646448T3 (pl) | 2010-11-29 | 2017-12-29 | OSI Pharmaceuticals, LLC | Makrocykliczne inhibitory kinazy |
| CN114989139A (zh) * | 2010-12-17 | 2022-09-02 | 诺华股份有限公司 | 制备嘧啶-2,4-二胺二盐酸盐的方法 |
| US8546443B2 (en) | 2010-12-21 | 2013-10-01 | Boehringer Ingelheim International Gmbh | Benzylic oxindole pyrimidines |
| JP2012153674A (ja) | 2011-01-28 | 2012-08-16 | Astellas Pharma Inc | ジ(アリールアミノ)アリール化合物の製造方法及びその合成中間体 |
| KR101521861B1 (ko) * | 2011-02-02 | 2015-05-21 | 노파르티스 아게 | Alk 억제제의 사용 방법 |
| DK2675793T3 (en) | 2011-02-17 | 2018-11-12 | Cancer Therapeutics Crc Pty Ltd | FAK INHIBITORS |
| WO2012110774A1 (en) | 2011-02-17 | 2012-08-23 | Cancer Therapeutics Crc Pty Limited | Selective fak inhibitors |
| EP2688883B1 (en) | 2011-03-24 | 2016-05-18 | Noviga Research AB | Pyrimidine derivatives |
| WO2012135641A2 (en) | 2011-03-30 | 2012-10-04 | H. Lee Moffitt Cancer Center And Research Institute | Aurora kinase inhibitors and methods of making and using thereof |
| SG194086A1 (en) | 2011-04-22 | 2013-11-29 | Signal Pharm Llc | Substituted diaminocarboxamide and diaminocarbonitrile pyrimidines, compositions thereof, and methods of treatment therewith |
| EP2704572B1 (en) | 2011-05-04 | 2015-12-30 | Ariad Pharmaceuticals, Inc. | Compounds for inhibiting cell proliferation in egfr-driven cancers |
| CA2853498A1 (en) | 2011-10-28 | 2013-05-02 | Celgene Avilomics Research, Inc. | Methods of treating a bruton's tyrosine kinase disease or disorder |
| EP2822935B1 (en) | 2011-11-17 | 2019-05-15 | Dana-Farber Cancer Institute, Inc. | Inhibitors of c-jun-n-terminal kinase (jnk) |
| EP2782579B1 (en) | 2011-11-23 | 2019-01-02 | Portola Pharmaceuticals, Inc. | Pyrazine kinase inhibitors |
| MX347772B (es) | 2012-03-06 | 2017-05-12 | Cephalon Inc | Derivado de 2,4-diaminopirimidina biciclico fusionado como un inhibidor dual de alk y fak. |
| BR112014022789B1 (pt) | 2012-03-15 | 2022-04-19 | Celgene Car Llc | Formas sólidas de um inibidor de quinase de receptor do fator de crescimento epidérmico, composição farmacêutica e usos do mesmo |
| RU2711077C9 (ru) | 2012-03-15 | 2020-08-11 | Селджен Кар Ллс | Соли ингибитора киназы рецептора эпидермального фактора роста |
| JP6469567B2 (ja) | 2012-05-05 | 2019-02-13 | アリアド・ファーマシューティカルズ・インコーポレイテッド | Egfr発動性がんの細胞増殖阻害用化合物 |
| US9676756B2 (en) | 2012-10-08 | 2017-06-13 | Portola Pharmaceuticals, Inc. | Substituted pyrimidinyl kinase inhibitors |
| US10112927B2 (en) | 2012-10-18 | 2018-10-30 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinase 7 (CDK7) |
| WO2014063061A1 (en) | 2012-10-19 | 2014-04-24 | Dana-Farber Cancer Institute, Inc. | Hydrophobically tagged small molecules as inducers of protein degradation |
| US10000483B2 (en) | 2012-10-19 | 2018-06-19 | Dana-Farber Cancer Institute, Inc. | Bone marrow on X chromosome kinase (BMX) inhibitors and uses thereof |
| AU2013337264B2 (en) | 2012-11-05 | 2018-03-08 | Foundation Medicine, Inc. | Novel fusion molecules and uses thereof |
| JP6359020B6 (ja) * | 2012-11-06 | 2018-08-15 | シャンハイ フォチョン ファーマシューティカル カンパニー リミテッド | Alkキナーゼ阻害剤 |
| CN103804299A (zh) * | 2012-11-14 | 2014-05-21 | 韩冰 | 一类具有神经保护作用的化合物及其用途 |
| WO2014100748A1 (en) | 2012-12-21 | 2014-06-26 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
| EP3939614A1 (en) | 2013-01-18 | 2022-01-19 | Foundation Medicine, Inc. | Methods of treating cholangiocarcinoma |
| EP2953457B1 (en) | 2013-02-08 | 2020-04-08 | Celgene CAR LLC | Erk inhibitors and uses thereof |
| HK1211235A1 (en) | 2013-02-22 | 2016-05-20 | 霍夫曼-拉罗奇有限公司 | Methods of treating cancer and preventing drug resistance |
| US9611283B1 (en) | 2013-04-10 | 2017-04-04 | Ariad Pharmaceuticals, Inc. | Methods for inhibiting cell proliferation in ALK-driven cancers |
| CA2912806A1 (en) | 2013-05-29 | 2014-12-04 | Cephalon, Inc. | Pyrrolotriazines as alk inhibitors |
| US20160129003A1 (en) | 2013-06-18 | 2016-05-12 | Novartis Ag | Pharmaceutical Combinations |
| TWI610923B (zh) * | 2013-07-11 | 2018-01-11 | Betta Pharmaceuticals Co Ltd | 酪氨酸蛋白激酶調節劑及其應用方法 |
| US9492471B2 (en) | 2013-08-27 | 2016-11-15 | Celgene Avilomics Research, Inc. | Methods of treating a disease or disorder associated with Bruton'S Tyrosine Kinase |
| WO2015038868A1 (en) * | 2013-09-13 | 2015-03-19 | Cephalon, Inc. | Fused bicyclic 2,4-diaminopyrimidine derivatives |
| RU2550346C2 (ru) | 2013-09-26 | 2015-05-10 | Общество с ограниченной ответственностью "Отечественные Фармацевтические Технологии" ООО"ФармТех" | Новые химические соединения (варианты) и их применение для лечения онкологических заболеваний |
| EP3057956B1 (en) | 2013-10-18 | 2021-05-05 | Dana-Farber Cancer Institute, Inc. | Polycyclic inhibitors of cyclin-dependent kinase 7 (cdk7) |
| ES2676734T3 (es) | 2013-10-18 | 2018-07-24 | Syros Pharmaceuticals, Inc. | Compuestos heteroatómicos útiles para el tratamiento de enfermedades proliferativas |
| AU2014346788B8 (en) | 2013-11-06 | 2021-01-28 | Arizona Board Of Regents On Behalf Of The Unviersity Of Arizona | Method for subtyping lymphoma types by means of expression profiling |
| US9415049B2 (en) | 2013-12-20 | 2016-08-16 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
| NZ715903A (en) | 2014-01-30 | 2017-06-30 | Signal Pharm Llc | Solid forms of 2-(tert-butylamino)-4-((1r,3r,4r)-3-hydroxy-4-methylcyclohexylamino)-pyrimidine-5-carboxamide, compositions thereof and methods of their use |
| WO2015164604A1 (en) * | 2014-04-23 | 2015-10-29 | Dana-Farber Cancer Institute, Inc. | Hydrophobically tagged janus kinase inhibitors and uses thereof |
| US10017477B2 (en) | 2014-04-23 | 2018-07-10 | Dana-Farber Cancer Institute, Inc. | Janus kinase inhibitors and uses thereof |
| EP3179858B1 (en) | 2014-08-13 | 2019-05-15 | Celgene Car Llc | Forms and compositions of an erk inhibitor |
| WO2016029002A2 (en) * | 2014-08-22 | 2016-02-25 | Clovis Oncology, Inc. | Growth factor receptor inhibitors |
| SG11201702980QA (en) | 2014-10-21 | 2017-05-30 | Ariad Pharma Inc | Crystalline forms of 5-chloro-n4-[-2-(dimethylphosphoryl) phenyl]-n2-{2-methoxy-4-[4-(4-methylpiperazin-1-yl) piperidin-1-yl] pyrimidine-2,4-diamine |
| WO2016100308A1 (en) | 2014-12-16 | 2016-06-23 | Signal Pharmaceuticals, Llc | Methods for measurement of inhibition of c-jun n-terminal kinase in skin |
| SG11201704827UA (en) | 2014-12-16 | 2017-07-28 | Signal Pharm Llc | Formulations of 2-(tert-butylamino)-4-((1r,3r,4r)-3-hydroxy-4-methycyclohexylamino)-pyrimidine-5-carboxamide |
| US10870651B2 (en) | 2014-12-23 | 2020-12-22 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinase 7 (CDK7) |
| ES2995737T3 (en) | 2015-01-06 | 2025-02-11 | Arena Pharm Inc | Compound for use in treating conditions related to the s1p1 receptor |
| EP3250557B1 (en) | 2015-01-29 | 2024-11-20 | Signal Pharmaceuticals, LLC | Isotopologues of 2-(tert-butylamino)-4-((1r,3r,4r)-3-hydroxy-4-methylcyclohexylamino)-pyrimidine-5-carboxamide |
| AU2016243529B2 (en) | 2015-03-27 | 2021-03-25 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinases |
| WO2016167511A2 (ko) * | 2015-04-14 | 2016-10-20 | 한국화학연구원 | N2-(2-메톡시페닐)피리미딘 유도체, 이의 제조 방법 및 이를 유효 성분으로 함유하는 암의 예방 또는 치료용 약학적 조성물 |
| US10702527B2 (en) | 2015-06-12 | 2020-07-07 | Dana-Farber Cancer Institute, Inc. | Combination therapy of transcription inhibitors and kinase inhibitors |
| MA42807A (fr) | 2015-06-22 | 2018-07-25 | Arena Pharm Inc | Sel l-arginine cristallin d'acide (r)-2-(7-(4-cyclopentyl-3-(trifluorométhyl)benzyloxy)-1,2,3,4-tétrahydrocyclo-penta[b]indol-3-yl)acétique (composé 1) pour une utilisation dans des troubles associés au récepteur de s1p1 |
| CN107922287B (zh) | 2015-07-24 | 2021-04-09 | 细胞基因公司 | 合成(1r,2r,5r)-5-氨基-2-甲基环己醇盐酸盐的方法和其中可用的中间体 |
| JP7028766B2 (ja) | 2015-09-09 | 2022-03-02 | ダナ-ファーバー キャンサー インスティテュート, インコーポレイテッド | サイクリン依存性キナーゼの阻害剤 |
| CN106699743B (zh) * | 2015-11-05 | 2020-06-12 | 湖北生物医药产业技术研究院有限公司 | 嘧啶类衍生物及其用途 |
| CN106883213B (zh) * | 2015-12-15 | 2021-04-20 | 合肥中科普瑞昇生物医药科技有限公司 | 一种egfr和alk激酶的双重抑制剂 |
| JP2019520382A (ja) * | 2016-06-27 | 2019-07-18 | 杭州雷索薬業有限公司Hangzhou Rex Pharmaceutical Co., Ltd | ベンゾフランピラゾールアミン類プロテインキナーゼ阻害薬 |
| WO2018044767A2 (en) | 2016-08-29 | 2018-03-08 | The Regents Of The University Of Michigan | Aminopyrimidines as alk inhibitors |
| KR101876514B1 (ko) * | 2016-11-08 | 2018-07-10 | 한국화학연구원 | 신규한 피리미딘화합물, 이의 제조방법 및 이를 유효성분으로 함유하는 암 및 염증질환의 예방 또는 치료용 약학적 조성물 |
| WO2018151873A1 (en) | 2017-02-16 | 2018-08-23 | Arena Pharmaceuticals, Inc. | Compounds and methods for treatment of primary biliary cholangitis |
| EP3586848B1 (en) | 2017-02-24 | 2021-09-01 | Daegu-Gyeongbuk Medical Innovation Foundation | Pharmaceutical composition comprising compound capable of penetrating blood-brain barrier as effective ingredient for preventing or treating brain cancer |
| JOP20190281A1 (ar) * | 2017-06-13 | 2019-12-02 | Korea Res Inst Chemical Tech | مشتق n2، n4 ثنائي فينيل بيريميدين -2، 4- ثنائي أمين، وطريقة لتحضيره، وتركيبة صيدلانية تحتوي على المشتق بوصفه مكون فعال للوقاية من السرطان أو علاجه |
| JP7356414B2 (ja) | 2017-09-07 | 2023-10-04 | レヴォリューション・メディスンズ,インコーポレイテッド | がんを治療するためのshp2阻害剤組成物および方法 |
| KR101992621B1 (ko) | 2017-12-07 | 2019-09-27 | 주식회사 온코빅스 | 암세포 성장 억제 효과를 나타내는 신규한 피리미딘 유도체 및 그를 포함하는 약제학적 조성물 |
| WO2019117813A1 (en) * | 2017-12-15 | 2019-06-20 | National University Of Singapore | Focal adhesion kinase targeted therapeutics for the treatment of glaucoma and fibrosis |
| JP7085242B2 (ja) * | 2017-12-21 | 2022-06-16 | 深▲チェン▼市塔吉瑞生物医薬有限公司 | キナーゼ活性を阻害するためのアリールホスフィンオキシド |
| CA3096984A1 (en) | 2018-04-05 | 2019-10-10 | Sumitomo Dainippon Pharma Oncology, Inc. | Axl kinase inhibitors and use of the same |
| EP3801459B1 (en) | 2018-06-06 | 2024-08-07 | Arena Pharmaceuticals, Inc. | Methods of treating conditions related to the s1p1 receptor |
| AU2019295632B2 (en) | 2018-06-25 | 2025-03-06 | Dana-Farber Cancer Institute, Inc. | Taire family kinase inhibitors and uses thereof |
| WO2020076723A1 (en) | 2018-10-08 | 2020-04-16 | Revolution Medicines, Inc. | Shp2 inhibitor compositions for use in treating cancer |
| CN112771032B (zh) * | 2018-10-29 | 2023-01-03 | 江苏先声药业有限公司 | 作为第四代egfr抑制剂的嘧啶吡唑类化合物 |
| US12415816B2 (en) | 2018-11-07 | 2025-09-16 | Dana-Farber Cancer Institute, Inc. | Benzothiazole derivatives and 7-aza-benzothiazole derivatives as janus kinase 2 inhibitors and uses thereof |
| JP7660063B2 (ja) | 2018-12-28 | 2025-04-10 | ダナ-ファーバー キャンサー インスティテュート, インコーポレイテッド | サイクリン依存性キナーゼ7のインヒビターおよびそれらの使用 |
| WO2020147702A1 (en) * | 2019-01-17 | 2020-07-23 | Betta Pharmaceuticals Co., Ltd | Egfr inhibitors, compositions and methods thereof |
| KR20210146288A (ko) | 2019-03-01 | 2021-12-03 | 레볼루션 메디슨즈, 인크. | 이환식 헤테로사이클릴 화합물 및 이의 용도 |
| US12187722B2 (en) | 2019-03-15 | 2025-01-07 | The General Hospital Corporation | Small molecule inhibitors of TEAD transcription factors |
| KR20210142154A (ko) | 2019-03-21 | 2021-11-24 | 옹쎄오 | 암 치료를 위한 키나제 억제제와 조합된 dbait 분자 |
| WO2021003417A1 (en) | 2019-07-03 | 2021-01-07 | Sumitomo Dainippon Pharma Oncology, Inc. | Tyrosine kinase non-receptor 1 (tnk1) inhibitors and uses thereof |
| KR102168179B1 (ko) * | 2019-10-31 | 2020-10-20 | 주식회사 온코빅스 | 암세포 성장 억제 효과를 나타내는 신규한 헤테로 고리 치환 피리미딘 유도체 및 그를 포함하는 약제학적 조성물 |
| US11566007B2 (en) | 2019-11-04 | 2023-01-31 | Revolution Medicines, Inc. | Ras inhibitors |
| EP4054720A1 (en) | 2019-11-04 | 2022-09-14 | Revolution Medicines, Inc. | Ras inhibitors |
| US11608346B2 (en) | 2019-11-04 | 2023-03-21 | Revolution Medicines, Inc. | Ras inhibitors |
| CN114761006A (zh) | 2019-11-08 | 2022-07-15 | Inserm(法国国家健康医学研究院) | 对激酶抑制剂产生耐药性的癌症的治疗方法 |
| EP4620531A3 (en) | 2019-11-08 | 2025-11-26 | Revolution Medicines, Inc. | Bicyclic heteroaryl compounds and uses thereof |
| WO2021111311A2 (ko) * | 2019-12-03 | 2021-06-10 | 삼진제약주식회사 | 국소 부착 키나아제 저해제로서 신규한 아다만탄 유도체 |
| WO2021142026A1 (en) | 2020-01-07 | 2021-07-15 | Revolution Medicines, Inc. | Shp2 inhibitor dosing and methods of treating cancer |
| WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
| AU2021227907A1 (en) * | 2020-02-25 | 2022-09-29 | Dana-Farber Cancer Institute, Inc. | Potent and selective degraders of ALK |
| TW202214253A (zh) | 2020-06-18 | 2022-04-16 | 美商銳新醫藥公司 | 延遲、預防及治療對ras抑制劑之後天抗性之方法 |
| IL301062A (en) | 2020-09-03 | 2023-05-01 | Revolution Medicines Inc | Use of sos1 inhibitors to treat malignancies with shp2 mutations |
| CR20230165A (es) | 2020-09-15 | 2023-06-02 | Revolution Medicines Inc | Derivados indólicos como inhibidores de ras en el tratamiento del cáncer |
| AR124449A1 (es) | 2020-12-22 | 2023-03-29 | Qilu Regor Therapeutics Inc | Inhibidores de sos1 y usos de los mismos |
| AU2022206470A1 (en) * | 2021-01-07 | 2023-07-27 | Ontario Institute For Cancer Research (Oicr) | Isoindolinone aminopyrimidine compounds as inhibitors of nuak kinases, compositions and uses thereof |
| WO2022211573A1 (ko) * | 2021-04-01 | 2022-10-06 | 주식회사 테라펙스 | 단백질 키나아제 저해 활성을 갖는 피리미딘 유도체 및 이를 포함하는 치료용 약학 조성물 |
| KR20240019071A (ko) | 2021-04-02 | 2024-02-14 | 브릿지바이오테라퓨틱스(주) | N2-페닐피리미딘-2,4-디아민 화합물, 및 그 제조 방법 및 사용 방법 |
| US20240382592A1 (en) | 2021-04-09 | 2024-11-21 | Institut National de la Santé et de la Recherche Médicale | Methods for the treatment of anaplastic large cell lymphoma |
| CN117500811A (zh) | 2021-05-05 | 2024-02-02 | 锐新医药公司 | 共价ras抑制剂及其用途 |
| CN118561952A (zh) | 2021-05-05 | 2024-08-30 | 锐新医药公司 | Ras抑制剂 |
| CR20230558A (es) | 2021-05-05 | 2024-01-24 | Revolution Medicines Inc | Inhibidores de ras para el tratamiento del cáncer |
| AR127308A1 (es) | 2021-10-08 | 2024-01-10 | Revolution Medicines Inc | Inhibidores ras |
| US12084453B2 (en) | 2021-12-10 | 2024-09-10 | Incyte Corporation | Bicyclic amines as CDK12 inhibitors |
| EP4448526A1 (en) | 2021-12-17 | 2024-10-23 | Genzyme Corporation | Pyrazolopyrazine compounds as shp2 inhibitors |
| EP4227307A1 (en) | 2022-02-11 | 2023-08-16 | Genzyme Corporation | Pyrazolopyrazine compounds as shp2 inhibitors |
| JP2025510572A (ja) | 2022-03-08 | 2025-04-15 | レボリューション メディシンズ インコーポレイテッド | 免疫不応性肺癌を治療するための方法 |
| EP4536364A1 (en) | 2022-06-10 | 2025-04-16 | Revolution Medicines, Inc. | Macrocyclic ras inhibitors |
| KR20240143136A (ko) | 2023-03-23 | 2024-10-02 | 청주대학교 산학협력단 | 콘크리트 양생용 광발열 단열시트 및 콘크리트 구조물의 조기 시공 방법 |
| AU2024241633A1 (en) | 2023-03-30 | 2025-11-06 | Revolution Medicines, Inc. | Compositions for inducing ras gtp hydrolysis and uses thereof |
| AR132338A1 (es) | 2023-04-07 | 2025-06-18 | Revolution Medicines Inc | Inhibidores de ras |
| AU2024252105A1 (en) | 2023-04-14 | 2025-10-16 | Revolution Medicines, Inc. | Crystalline forms of ras inhibitors, compositions containing the same, and methods of use thereof |
| KR20250172857A (ko) | 2023-04-14 | 2025-12-09 | 레볼루션 메디슨즈, 인크. | Ras 억제제의 결정형 |
| WO2024229406A1 (en) | 2023-05-04 | 2024-11-07 | Revolution Medicines, Inc. | Combination therapy for a ras related disease or disorder |
| WO2024251270A1 (zh) * | 2023-06-08 | 2024-12-12 | 希格生科(深圳)有限公司 | 含氮芳环化合物及其医药用途 |
| WO2025034702A1 (en) | 2023-08-07 | 2025-02-13 | Revolution Medicines, Inc. | Rmc-6291 for use in the treatment of ras protein-related disease or disorder |
| TW202530228A (zh) | 2023-10-12 | 2025-08-01 | 美商銳新醫藥公司 | Ras抑制劑 |
| WO2025137507A1 (en) | 2023-12-22 | 2025-06-26 | Regor Pharmaceuticals, Inc. | Sos1 inhibitors and uses thereof |
| WO2025171296A1 (en) | 2024-02-09 | 2025-08-14 | Revolution Medicines, Inc. | Ras inhibitors |
| 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 (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0105400A1 (en) * | 1982-09-30 | 1984-04-18 | Mitsubishi Denki Kabushiki Kaisha | Process for preparing a heat resistant soft composite |
| WO2003018021A1 (en) * | 2001-08-22 | 2003-03-06 | Amgen Inc. | 2,4-disubstituted pyrimidinyl derivatives for use as anticancer agents |
| WO2003030909A1 (en) * | 2001-09-25 | 2003-04-17 | Bayer Pharmaceuticals Corporation | 2- and 4-aminopyrimidines n-substtituded by a bicyclic ring for use as kinase inhibitors in the treatment of cancer |
| WO2003063794A2 (en) * | 2002-02-01 | 2003-08-07 | Rigel Pharmaceuticals, Inc. | 2,4-pyrimidinediamine compounds and their uses |
Family Cites Families (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL129020C (enExample) | 1964-12-15 | |||
| US3432493A (en) | 1966-06-27 | 1969-03-11 | Abbott Lab | Substituted sulfanilamides |
| SU194829A1 (ru) * | 1966-07-08 | 1967-04-12 | Замещенных 5,6-дигидропирроло- | |
| US3367149A (en) * | 1966-12-15 | 1968-02-06 | Minnesota Mining & Mfg | Radiant white light source |
| EP0002341B1 (en) * | 1977-11-28 | 1982-01-20 | Barry Boettcher | Complexes of bivalent copper, methods of preparation thereof and compositions containing said complexes |
| GB9523675D0 (en) | 1995-11-20 | 1996-01-24 | Celltech Therapeutics Ltd | Chemical compounds |
| GB9619284D0 (en) | 1996-09-16 | 1996-10-30 | Celltech Therapeutics Ltd | Chemical compounds |
| GB9622363D0 (en) | 1996-10-28 | 1997-01-08 | Celltech Therapeutics Ltd | Chemical compounds |
| GB9705361D0 (en) | 1997-03-14 | 1997-04-30 | Celltech Therapeutics Ltd | Chemical compounds |
| WO1999031073A1 (en) * | 1997-12-15 | 1999-06-24 | Yamanouchi Pharmaceutical Co., Ltd. | Novel pyrimidine-5-carboxamide derivatives |
| ATE232521T1 (de) * | 1998-03-27 | 2003-02-15 | Janssen Pharmaceutica Nv | Hiv hemmende pyrimidin derivate |
| EP1107957B1 (en) * | 1998-08-29 | 2006-10-18 | AstraZeneca AB | Pyrimidine compounds |
| GB9828511D0 (en) | 1998-12-24 | 1999-02-17 | Zeneca Ltd | Chemical compounds |
| EP1184376B1 (en) * | 1999-06-09 | 2005-02-02 | Yamanouchi Pharmaceutical Co. Ltd. | Novel heterocyclic carboxamide derivatives |
| JP4622047B2 (ja) * | 1999-06-09 | 2011-02-02 | アステラス製薬株式会社 | 新規なヘテロ環カルボキサミド誘導体 |
| CA2386218A1 (en) | 1999-10-07 | 2001-04-12 | Amgen Inc. | Triazine kinase inhibitors |
| US20030004174A9 (en) | 2000-02-17 | 2003-01-02 | Armistead David M. | Kinase inhibitors |
| US6376770B1 (en) * | 2000-02-28 | 2002-04-23 | Douglas Hyde | Quick connecting universal electrical box and wiring system |
| GB0004888D0 (en) | 2000-03-01 | 2000-04-19 | Astrazeneca Uk Ltd | Chemical compounds |
| GB0004887D0 (en) * | 2000-03-01 | 2000-04-19 | Astrazeneca Uk Ltd | Chemical compounds |
| GB0004890D0 (en) * | 2000-03-01 | 2000-04-19 | Astrazeneca Uk Ltd | Chemical compounds |
| US20020132823A1 (en) | 2001-01-17 | 2002-09-19 | Jiahuai Han | Assay method |
| EP1406875B1 (en) * | 2001-06-26 | 2013-07-31 | Bristol-Myers Squibb Company | N-heterocyclic inhibitors of tnf-alpha expression |
| JO3429B1 (ar) * | 2001-08-13 | 2019-10-20 | Janssen Pharmaceutica Nv | مشتقات برميدينات مثبطة فيروس الايدز |
| CA2463823A1 (en) * | 2001-11-01 | 2003-05-08 | Janssen Pharmaceutica N.V. | Aminobenzamide derivatives as glycogen synthase kinase 3.beta. inhibitors |
| US7459455B2 (en) * | 2002-02-08 | 2008-12-02 | Smithkline Beecham Corporation | Pyrimidine compounds |
| GB0206215D0 (en) * | 2002-03-15 | 2002-05-01 | Novartis Ag | Organic compounds |
| WO2003095448A1 (en) * | 2002-05-06 | 2003-11-20 | Bayer Pharmaceuticals Corporation | Pyridinyl amino pyrimidine derivatives useful for treating hyper-proliferative disorders |
| CN1665789A (zh) * | 2002-06-28 | 2005-09-07 | 山之内制药株式会社 | 二氨基嘧啶酰胺衍生物 |
| ATE451104T1 (de) * | 2002-07-29 | 2009-12-15 | Rigel Pharmaceuticals Inc | Verfahren zur behandlung oder pruvention von autoimmunkrankheiten mit 2,4-pyrimidindiamin- verbindungen |
| UA80767C2 (en) | 2002-12-20 | 2007-10-25 | Pfizer Prod Inc | Pyrimidine derivatives for the treatment of abnormal cell growth |
| KR20110132482A (ko) * | 2003-02-07 | 2011-12-07 | 얀센 파마슈티카 엔.브이. | Hiv 감염 예방용 피리미딘 유도체 |
| EP1597251B1 (en) * | 2003-02-20 | 2009-06-10 | SmithKline Beecham Corporation | Pyrimidine compounds |
| GB0305929D0 (en) * | 2003-03-14 | 2003-04-23 | Novartis Ag | Organic compounds |
| CA2531333A1 (en) * | 2003-07-16 | 2005-02-10 | Janssen Pharmaceutica N.V. | Triazolopyrimidine derivatives as glycogen synthase kinase 3 inhibitors |
| US7449465B2 (en) * | 2003-07-16 | 2008-11-11 | Janssen Pharmaceutica, N.V. | Triazolopyrimidine derivatives as glycogen synthase kinase 3 inhibitors |
| EP1663242B1 (en) * | 2003-08-07 | 2011-04-27 | Rigel Pharmaceuticals, Inc. | 2,4-pyrimidinediamine compounds and uses as anti-proliferative agents |
| DK2287156T3 (da) * | 2003-08-15 | 2013-08-26 | Novartis Ag | 2,4-Di(phenylamino)-pyrimidiner egnede i behandling af neoplastiske sygdomme, inflammatoriske lidelser og lidelser i immunsystemet |
| GB0321710D0 (en) * | 2003-09-16 | 2003-10-15 | Novartis Ag | Organic compounds |
| JP2007505858A (ja) * | 2003-09-18 | 2007-03-15 | ノバルティス アクチエンゲゼルシャフト | 増殖性障害の処置に有用な2,4−ジ(フェニルアミノ)ピリミジン |
| WO2006068770A1 (en) | 2004-11-24 | 2006-06-29 | Rigel Pharmaceuticals, Inc. | Spiro-2, 4-pyrimidinediamine compounds and their uses |
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Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0105400A1 (en) * | 1982-09-30 | 1984-04-18 | Mitsubishi Denki Kabushiki Kaisha | Process for preparing a heat resistant soft composite |
| WO2003018021A1 (en) * | 2001-08-22 | 2003-03-06 | Amgen Inc. | 2,4-disubstituted pyrimidinyl derivatives for use as anticancer agents |
| WO2003030909A1 (en) * | 2001-09-25 | 2003-04-17 | Bayer Pharmaceuticals Corporation | 2- and 4-aminopyrimidines n-substtituded by a bicyclic ring for use as kinase inhibitors in the treatment of cancer |
| WO2003063794A2 (en) * | 2002-02-01 | 2003-08-07 | Rigel Pharmaceuticals, Inc. | 2,4-pyrimidinediamine compounds and their uses |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013176503A1 (ko) | 2012-05-24 | 2013-11-28 | 서울대학교 산학협력단 | 타우 단백질 매개 신경 퇴행성 질환 치료제 |
| WO2014025128A1 (ko) * | 2012-08-10 | 2014-02-13 | 한국화학연구원 | N2,n4-비스(4-(피페라진-1-일)페닐)피리미딘-2,4-디아민 유도체 또는 이의 약학적으로 허용 가능한 염 및 이를 유효성분으로 함유하는 암의 예방 또는 치료용 약학적 조성물 |
| US9199944B2 (en) | 2012-08-10 | 2015-12-01 | Korea Research Institute Of Chemical Technology | N2,N4-bis(4-(piperazine-1-yl)phenyl)pirimidine-2,4-diamine derivative or pharmaceutically acceptable salt thereof, and composition containing same as active ingredient for preventing or treating cancer |
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