Release Time:2019-03-09 Hits:
Indexed by: Journal Article
Date of Publication: 2011-02-24
Journal: JOURNAL OF MEDICINAL CHEMISTRY
Included Journals: PubMed、SCIE、Scopus
Volume: 54
Issue: 4
Page Number: 1101-1105
ISSN: 0022-2623
Abstract: We recently described the discovery of a dual inhibitor of Bcl-2 and Mcl-1, 3-thiomorpholin-8-oxo-8H-acenaphtho[1,2-b]pyrrole-9-carbonitrile (3, S1). Here we report a structure-guided design in combination with structure activity relationship studies to exploit the difference in the p2 binding pocket of Bcl-2 and Mcl-1, from which a novel dual inhibitor 3-(4-aminophenylthio)-8-oxo-8H-acenaphtho[1,2-b]pyrrole-9-carbonitrile (6h) was obtained, which showed significant enhanced IC(50) value against Mcl-1 (5 nM), greater Mcl-1/Bak disruption potential, and accordingly a 10-fold increased cytotoxicity over 3.