Discovery of a Potent Boronic Acid Derived Inhibitor of the HCV RNA-Dependent RNA Polymerase

被引:41
|
作者
Maynard, Andrew [2 ]
Crosby, Renae M. [1 ]
Ellis, Byron [2 ]
Hamatake, Robert [1 ]
Hong, Zhi [1 ]
Johns, Brian A. [1 ]
Kahler, Kirsten M. [2 ]
Koble, Cecilia [1 ]
Leivers, Anna [1 ]
Leivers, Martin R. [1 ]
Mathis, Amanda [1 ]
Peat, Andrew J. [1 ]
Pouliot, Jeffrey J. [1 ]
Roberts, Christopher D. [1 ]
Samano, Vicente [1 ]
Schmidt, Rachel M. [2 ]
Smith, Gary K. [2 ]
Spaltenstein, Andrew [1 ]
Stewart, Eugene L. [2 ]
Thommes, Pia [3 ]
Turner, Elizabeth M. [1 ]
Voitenleitner, Christian [1 ]
Walker, Jill T. [1 ]
Waitt, Greg [2 ]
Weatherhead, Jason [1 ]
Weaver, Kurt [2 ]
Williams, Shawn [2 ]
Wright, Lois [2 ]
Xiong, Zhiping Z. [1 ]
Haigh, David [3 ]
Shotwell, J. Brad [1 ]
机构
[1] GlaxoSmithKline, Infect Dis Med Discovery Unit, Res Triangle Pk, NC 27709 USA
[2] GlaxoSmithKline, Platform Technol & Sci, Res Triangle Pk, NC 27709 USA
[3] GlaxoSmithKline, Infect Dis Ctr Excellence Drug Discovery, Stevenage SG1 1NY, Herts, England
关键词
HEPATITIS-C VIRUS; NONNUCLEOSIDE INHIBITORS; ANTIFUNGAL AGENT; RESISTANCE; MECHANISMS; NUCLEOTIDE; INITIATION; PROTEASE; SITE;
D O I
10.1021/jm400317w
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A boronic acid moiety was found to be a critical pharmacophore for enhanced in vitro potency against wild-type hepatitis C replicons and known clinical polymorphic and resistant HCV mutant replicons. The synthesis, optimization, and structure-activity relationships associated with inhibition of HCV replication in a subgenomic replication system for a series of non-nucleoside boron-containing HCV RNA-dependent RNA polymerase (NS5B) inhibitors are described. A summary of the discovery of 3 (GSK5852), a molecule which entered clinical trials in subjects infected with HCV in 2011, is included.
引用
收藏
页码:1902 / 1913
页数:12
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