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"pyrrolopyrimidines used as kinase inhibitors"
专利权人:
发明人:
EDWARD GILES MCIVER AND JOANE HOUGH
申请号:
IN6428/DELNP/2011
公开号:
IN2011DN06428A
申请日:
2011.08.24
申请国别(地区):
IN
年份:
2012
代理人:
摘要:
The invention relates to a compound of formula (I), or a pharmaceutically acceptable salt or ester thereof, wherein R1 is -NR7(CO)R11 R2 is aryl, heteroaryl, fused aryl-C3-6-heterocycloalkyl or fused heteroaryl-C3-6- heterocycloalkyl, each of which is optionally substituted each R7 is selected from hydrogen, C1-6-alkyl and C3-7-cycloalkyl, wherein said C1-6-alkyl is optionally substituted by one or more halogens each R1, is independently selected from C1-6-alkyl, C3-7-xycloalkyl, C1-6alkyl-C3-7-cycloalkyl, C^-heterocycloalkyl, aryl and heteroaryl, each of winch may be optionally substituted. Further aspects of the invention relate to harmaceutical compositions comprising the same, and methods for treating or preventing a disorder selected from cancer, septic hock, Primary open Angle Glaucoma (POAG), hyperplasia, rheumatoid arthritis, psoriasis, artberosclerosis, retinopathy, os-eoarthritis, endometriosis, chronic inflammation and Alzheimer"s disease. Another aspect of the invention relates to the use of a compound as described above in the preparation of a medicament for the prevention or treatment of a disorder caused by, associat-d with or accompanied by any abnormal kinase activity, wherein the kinase is selected from TBK1, ERK8, CDK2, MARIO, ESI, VEG-FR, IKKepsilon and combinations thereof.
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中国工程科技知识中心
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