Azole-based inhibitors of AKT/PKB for the treatment of cancer
摘要:
Through a combination of screening and structure-based rational design, we have discovered a series of N-1-(5-(heterocyclyl)-thiazol-2-yl)-3-(4-trifluoromethylphenyl)-1,2-propanediamines that were developed into potent ATP competitive inhibitors of AKT. Studies of linker strand-binding adenine isosteres identified SAR trends in potency and selectivity that were consistent with binding interactions observed in structures of the inhibitors bound to AKT1 and to the counter-screening target PKA. One compound was shown to have acceptable pharmacokinetic properties and to be a potent inhibitor of AKT signaling and of in vivo xenograft tumor growth in a preclinical model of glioblastoma. (C) 2010 Elsevier Ltd. All rights reserved.
THIAZOLE COMPOUNDS AS PROTEIN KINASE B (PKB) INHIBITORS
申请人:Amgen, Inc
公开号:EP1981884B1
公开(公告)日:2012-06-13
US7514566B2
申请人:——
公开号:US7514566B2
公开(公告)日:2009-04-07
US8084479B2
申请人:——
公开号:US8084479B2
公开(公告)日:2011-12-27
[EN] THIAZOLE COMPOUNDS AND METHODS OF USE<br/>[FR] COMPOSES THIAZOLE ET PROCEDES D'UTILISATION
申请人:AMGEN INC
公开号:WO2007084391A2
公开(公告)日:2007-07-26
[EN] The invention relates to thiazole compounds of Formula (I) and Formula (II) and compositions thereof useful for treating diseases mediated by protein kinase B (PKB) where the variables have the definitions provided herein. The invention also relates to the therapeutic use of such thiazole compounds and compositions thereof in treating disease states associated with abnormal cell growth, cancer, inflammation, and metabolic disorders. [FR] La présente invention concerne des composés thiazole de formule (I) et formule (II), ainsi que des compositions les comprenant utiles pour traiter les maladies liées à l'activité de la protéine kinase B (PKB). Dans ces formules, les variables sont telles que définies dans la description. L'invention concerne également l'utilisation thérapeutique desdits composés thiazole et de compositions les contenant pour le traitement d'états maladifs associés à la prolifération anormale des cellules, aux cancers, aux inflammations et aux troubles métaboliques.