Targeting the PPM1D phenotype; 2,4-bisarylthiazoles cause highly selective apoptosis in PPM1D amplified cell-lines
摘要:
The metal-dependent phosphatase PPM1D (WIP1) is an important oncogene in cancer, with over-expression of the protein being associated with significantly worse clinical outcomes. In this communication we describe the discovery and optimization of novel 2,4-bisarylthiazoles that phenocopy the knockdown of PPM1D, without inhibiting its phosphatase activity. These compounds cause growth inhibition at nanomolar concentrations, induce apoptosis, activate p53 and display impressive cell-line selectivity. The results demonstrate the potential for targeting phenotypes in drug discovery when tackling challenging targets or unknown mechanisms. (C) 2014 Published by Elsevier Ltd.
[EN] FUSED HETEROCYCLIC COMPOUNDS AND THEIR USE<br/>[FR] COMPOSÉS HÉTÉROCYCLIQUES FONDUS ET UTILISATION DESDITS COMPOSÉS
申请人:CANCER RES INST ROYAL
公开号:WO2014030001A1
公开(公告)日:2014-02-27
The present invention provides compounds of formula (I) and pharmaceutically acceptable salts, hydrates and solvates thereof for use in the treatment of cancer:
申请人:The Institute of Cancer Research: Royal Cancer Hospital
公开号:US20150232462A1
公开(公告)日:2015-08-20
The present invention provides compounds of formula (I) and pharmaceutically acceptable salts, hydrates and solvates thereof for use in the treatment of cancer: