Discovery of novel potent HCV NS5B polymerase non-nucleoside inhibitors bearing a fused benzofuran scaffold

被引:21
|
作者
Zhong, Min [1 ]
Peng, Eric [1 ]
Huang, Ningwu [1 ]
Huang, Qi [1 ]
Huq, Anja [1 ]
Lau, Meiyen [1 ]
Colonno, Richard [1 ]
Li, Leping [1 ]
机构
[1] Presidio Pharmaceut Inc, 1700 Owens St,Suite 184, San Francisco, CA 94158 USA
关键词
HCV; NS5B polymerase; Non-nucleoside inhibitor; Fused benzofuran; HEPATITIS-C VIRUS; H-1-NMR ANISOTROPY METHOD; PROTEASE INHIBITOR; 2-METHOXY-2-(1-NAPHTHYL)PROPIONIC ACID; ABSOLUTE-CONFIGURATIONS; NS3/4A PROTEASE; IN-VITRO; NON-A; INFECTION; ENANTIORESOLUTION;
D O I
10.1016/j.bmcl.2018.01.029
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
This letter describes the discovery of a fused benzofuran scaffold viable for preparing a series of novel potent HCV NS5B polymerase non-nucleoside inhibitors. Designed on the basis of the functionalized benzofuran derivative nesbuvir (HCV-796), these compounds presumably bind similarly to the allosteric binding site in the "palm" domain of HCV NS5B protein. SAR of each potential hydrogen-bonding interaction site of this novel scaffold is discussed along with some preliminary genotypic profile and PK data of several advanced compounds. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:963 / 968
页数:6
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