Optimization of the indolyl quinolinone class of KDR (VEGFR-2) kinase inhibitors
摘要:
Modifications to the basic side-chain of early lead structures of the indolyl quinolinone class of KDR kinase inhibitors resulted in improved pharmacokinctic and ancillary profiles. Specifically, compounds bearing 5-amido- and 5-sulphonamido-indolyl substituents exhibited lower plasma clearance and weaker binding affinity for the I-Kr potassium channel hERG. (C) 2003 Elsevier Science Ltd. All rights reserved. (C) 2003 Elsevier Ltd. All rights reserved.
[EN] TYROSINE KINASE INHIBITORS<br/>[FR] INHIBITEURS DE TYROSINES KINASES
申请人:MERCK & CO INC
公开号:WO2003037252A2
公开(公告)日:2003-05-08
The present invention relates to compounds which inhibit, regulate and/or modulate tyrosine kinase signal transduction, compositions which contain these compounds, and methods of using them to treat tyrosine kinase-dependent diseases and conditions, such as angiogenesis, cancer, tumor growth, atherosclerosis, age related macular degeneration, diabetic retinopathy, inflammatory diseases, and the like in mammals.