期刊
CHEMMEDCHEM
卷 3, 期 6, 页码 914-923出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cmdc.200800010
关键词
isoquinolinones; medicinal chemistry; molecular docking; PARP-2 inhibitors; poly(ADP-ribosyl)ation
PARP-1 and PARP-2 are members of the family of poly(ADP-ribose)polymeroses, which are involved in the maintenance of genomic integrity under conditions of genotoxic stimuli. The different roles of the two isoforms under pathophysiological conditions have not yet been fully clarified, and this is partially due to the lack of selective inhibitors. We report herein the synthesis and preliminary pharmacological evaluation of a large series of isoquinolinone derivatives as PARP-1/PARP-2 inhibitors. Among them, we identified the 5-benzoyloxyisoquinolin-1(2H)-one derivative as the most selective PARP-2 inhibitor reported so for, with a PARP-2/PARP-1 selectivity index greater than 60.
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