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公开(公告)号:WO2002064586A3
公开(公告)日:2002-08-22
申请号:PCT/US2002/003791
申请日:2002-02-08
Applicant: VERTEX PHARMACEUTICALS INCORPORATED , CAO, Jingrong , GREEN, Jeremy , HALE, Michael , MALTAIS, Francois , STRAUB, Judy , TANG, Qing , ARONOV, Alex
Inventor: CAO, Jingrong , GREEN, Jeremy , HALE, Michael , MALTAIS, Francois , STRAUB, Judy , TANG, Qing , ARONOV, Alex
IPC: C07D403/04
Abstract: Described herein are compounds that are useful as protein kinase inhibitors having the formula (I) wherein Z 1 and Z 2 are each independently nitrogen or CH and Ring A, T m R 1 , QR 2 , U n R 3 , and Sp are as described in the specification. The compounds are especially useful as inhibitors of ERK2 and for treating diseases in mammals that are alleviated by a protein kinase inhibitor, particularly diseases such as cancer, inflammatory disorders, restenosis, diabetes, and cardiovascular disease.
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公开(公告)号:WO02064586A2
公开(公告)日:2002-08-22
申请号:PCT/US0203791
申请日:2002-02-08
Applicant: VERTEX PHARMA , CAO JINGRONG , GREEN JEREMY , HALE MICHAEL , MALTAIS FRANCOIS , STRAUB JUDY , TANG QING , ARONOV ALEX
Inventor: CAO JINGRONG , GREEN JEREMY , HALE MICHAEL , MALTAIS FRANCOIS , STRAUB JUDY , TANG QING , ARONOV ALEX
IPC: A61K31/506 , A61K31/517 , A61K31/5377 , A61K31/551 , A61P1/16 , A61P3/10 , A61P5/00 , A61P7/02 , A61P9/08 , A61P9/10 , A61P17/06 , A61P19/00 , A61P25/00 , A61P25/28 , A61P29/00 , A61P31/04 , A61P31/12 , A61P35/00 , A61P37/06 , A61P37/08 , A61P43/00 , C07D401/14 , C07D403/04 , C07D403/14 , C07D405/14 , C07D413/14
CPC classification number: C07D401/14 , C07D403/04 , C07D403/14 , C07D405/14 , C07D413/14
Abstract: Described herein are compounds that are useful as protein kinase inhibitors having the formula (I) wherein Z and Z are each independently nitrogen or CH and Ring A, TmR , QR , UnR , and Sp are as described in the specification. The compounds are especially useful as inhibitors of ERK2 and for treating diseases in mammals that are alleviated by a protein kinase inhibitor, particularly diseases such as cancer, inflammatory disorders, restenosis, diabetes, and cardiovascular disease.
Abstract translation: 本文描述了可用作具有式(I)的蛋白激酶抑制剂的化合物,其中Z 1和Z 2各自独立地为氮或CH,环A,TmR 1,QR 2,UnR 3 >和Sp如说明书中所述。 该化合物特别可用作ERK2的抑制剂,并且用于治疗由蛋白激酶抑制剂,特别是癌症,炎性疾病,再狭窄,糖尿病和心血管疾病等疾病缓解的哺乳动物疾病。
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