468741-06-2Relevant articles and documents
Imidazole moiety replacements in the 3-(1H-benzo[d]imidazol-2-yl)pyridin-2(1H)-one inhibitors of insulin-like growth factor receptor-1 (IGF-1R) to improve cytochrome P450 profile
Velaparthi, Upender,Liu, Peiying,Balasubramanian, Balu,Carboni, Joan,Attar, Ricardo,Gottardis, Marco,Li, Aixin,Greer, Ann,Zoeckler, Mary,Wittman, Mark D.,Vyas, Dolatrai
, p. 3072 - 3076 (2007)
A series of 3-(1H-benzo[d]imidazol-2-yl)pyridin-2(1H)-one inhibitors of insulin-like growth factor receptor-1 (IGF-1R) were examined in which the pendant imidazole moiety was replaced to improve selectivity for IGF-1R inhibition over cytochrome P450 (CYP). Synthesis and SAR of these compounds is presented.
Novel tyrosine kinase inhibitors
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Page 28, (2010/11/30)
The present invention provides compounds of formula I and pharmaceutically acceptable salts thereof. The formula I compounds inhibit tyrosine kinase enzymes thereby making them useful as anti-cancer agents. The formula I compounds are also useful for the treatment of other diseases which can be treated by inhibiting tyrosine kinase enzymes.