化学
效力
热休克蛋白70
腺苷
热休克蛋白
热休克蛋白90
结构-活动关系
细胞生长
体外
化学合成
立体化学
生物化学
基因
作者
D.S. Williamson,Jenifer Borgognoni,Alexandra Clay,Zoe Daniels,P. Dokurno,Martin J. Drysdale,Nicolas Foloppe,Geraint L. Francis,Christopher J Graham,Rob Howes,Alba T. Macias,James B. Murray,Rachel Parsons,T. Shaw,A.E. Surgenor,Lindsey Terry,Yikang Wang,Mike Wood,Andrew J. Massey
摘要
The design and synthesis of novel adenosine-derived inhibitors of HSP70, guided by modeling and X-ray crystallographic structures of these compounds in complex with HSC70/BAG-1, is described. Examples exhibited submicromolar affinity for HSP70, were highly selective over HSP90, and some displayed potency against HCT116 cells. Exposure of compound 12 to HCT116 cells caused significant reduction in cellular levels of Raf-1 and Her2 at concentrations similar to that which caused cell growth arrest.
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