化学
聚ADP核糖聚合酶
苯甲酰胺
共晶
立体化学
核糖
体外
三环
酶
生物化学
聚合酶
分子
氢键
有机化学
作者
Stacie S. Canan Koch,Lars Thoresen,Jayashree Tikhe,Karen A. Maegley,Robert J. Almassy,Jianke Li,Xiaohong Yu,Scott E. Zook,Robert A. Kumpf,Cathy Zhang,Theodore J. Boritzki,Rena N. Mansour,Kanyin E. Zhang,Anne Ekker,Chris R. Calabrese,Nicola J. Curtin,Suzanne Kyle,Huw D. Thomas,Lan-Zhen Wang,A. Hilary Calvert
摘要
A series of novel compounds have been designed that are potent inhibitors of poly(ADP-ribose) polymerase-1 (PARP-1), and the activity and physical properties have been characterized. The new structural classes, 3,4,5,6-tetrahydro-1H-azepino[5,4,3-cd]indol-6-ones and 3,4-dihydropyrrolo[4,3,2-de]isoquinolin-5-(1H)-ones, have conformationally locked benzamide cores that specifically interact with the PARP-1 protein. The compounds have been evaluated with in vitro cellular assays that measure the ability of the PARP-1 inhibitors to enhance the effect of cytotoxic agents against cancer cell lines.
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