[EN] SUBSTITUTED CYCLIC UREA DERIVATIVES, PREPARATION THEREOF AND PHARMACEUTICAL USE THEREOF AS KINASE INHIBITORS [FR] DERIVES D'UREE CYCLIQUES SUBSTITUES, PREPARATION ET UTILISATION PHARMACEUTIQUE DE CES DERIVES EN TANT QU'INHIBITEURS DE KINASES
Synthesis and optimization of substituted furo[2,3-d]-pyrimidin-4-amines and 7H-pyrrolo[2,3-d]pyrimidin-4-amines as ACK1 inhibitors
摘要:
Two classes of ACK1 inhibitors, 4,5,6-trisubstituted furo[2,3-d]pyrimidin4-amines and 4,5,6-trisubstituted 7H-pyrrolo[2,3-d]pyrimidin-4-amines, were discovered and evaluated as ACK1 inhibitors. Further structural refinement led to the identification of potent and selective dithiolane inhibitor 37. (C) 2012 Published by Elsevier Ltd.
Pyrrolo[2,3-d]pyrimidines that modulate ACK1 activity
申请人:Farthing N. Christopher
公开号:US20060040965A1
公开(公告)日:2006-02-23
Compounds that modulate the action of ACK1 and LCK, and related compositions methods for treating ACK1- and LCK-mediated diseases are described. In one aspect, the compounds have the general structure:
where the values of the substituents are provided herein.