Development of Glucose Regulated Protein 94-Selective Inhibitors Based on the BnIm and Radamide Scaffold
作者:Vincent M. Crowley、Anuj Khandelwal、Sanket Mishra、Andrew R. Stothert、Dustin J. E. Huard、Jinbo Zhao、Aaron Muth、Adam S. Duerfeldt、James L. Kizziah、Raquel L. Lieberman、Chad A. Dickey、Brian S. J. Blagg
DOI:10.1021/acs.jmedchem.6b00085
日期:2016.4.14
that was used to design isoform-selective inhibitors. Incorporation of a cis-amide bioisostere into the radamide scaffold led to development of the original Grp94-selective inhibitor, BnIm. Structure–activityrelationship studies have now been performed on the aryl side chain of BnIm, which resulted in improved analogues that exhibit better potency and selectivity for Grp94. These analogues also manifest