Antiviral activity and resistance of HCV NS5A replication complex inhibitors

被引:115
作者
Gao, Min [1 ]
机构
[1] Bristol Myers Squibb Co, Wallingford, CT 06492 USA
关键词
HEPATITIS-C-VIRUS; NONSTRUCTURAL PROTEIN 5A; RNA REPLICATION; IN-VITRO; BMS-790052; PHOSPHORYLATION; DOMAIN; IDENTIFICATION; VARIANTS; MODES;
D O I
10.1016/j.coviro.2013.06.014
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Treatment of Hepatitis C Virus (HCV) infection is rapidly evolving with the introduction of direct acting antiviral agents (DAA). HCV NS5A replication complex inhibitors, exemplified by Daclatasvir (BMS-790052), represent a new class of DAA. The exceptional in vitro potency (EC50 values at pM to low nM range) and broad genotype coverage of NS5A inhibitors have translated to robust anti-HCV effects in infected patients, making NS5A inhibitors an essential component of effective HCV DAA combination therapies. On the basis of drug-induced resistance substitutions and computer modeling, NS5A inhibitors most likely act at the N-terminus of NS5A (domain l). Mechanism of inhibition studies to elucidate the exquisite potency of these inhibitors have generated several working models.
引用
收藏
页码:514 / 520
页数:7
相关论文
共 56 条
[1]   Mutational analysis of hepatitis C virus nonstructural protein 5A: Potential role of differential phosphorylation in RNA replication and identification of a genetically flexible domain [J].
Appel, N ;
Pietschmann, T ;
Bartenschlager, R .
JOURNAL OF VIROLOGY, 2005, 79 (05) :3187-3194
[2]   Essential role of domain III of nonstructural protein 5A for hepatitis C virus infectious particle assembly [J].
Appel, Nicole ;
Zayas, Margarita ;
Miller, Sven ;
Krijnse-Locker, Jacomine ;
Schaller, Torsten ;
Friebe, Peter ;
Kallis, Stephanie ;
Engel, Ulrike ;
Bartenschlager, Ralf .
PLOS PATHOGENS, 2008, 4 (03)
[3]  
Bechtel J, 2011, 46 EASL BERL GERM
[4]   Small molecule inhibitors of the hepatitis C virus-encoded NS5A protein [J].
Belda, Oscar ;
Targett-Adams, Paul .
VIRUS RESEARCH, 2012, 170 (1-2) :1-14
[5]  
Bilello JP, 2011, 18 INT S HEP C VIR R
[6]   An amino-terminal amphipathic α-helix mediates membrane association of the hepatitis C virus nonstructural protein 5A [J].
Brass, V ;
Bieck, E ;
Montserret, R ;
Wölk, B ;
Hellings, JA ;
Blum, HE ;
Penin, F ;
Moradpour, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (10) :8130-8139
[7]  
Cheng G, 2013, 48 EASL AMST NETH
[8]  
Cheng G, 2012, 47 EASL BARC SPAIN
[9]  
Colonno R, 2011, 46 EASL BERL GERM
[10]   Synthesis and SAR of piperazinyl-N-phenylbenzamides as inhibitors of hepatitis C virus RNA replication in cell culture [J].
Conte, Immacolata ;
Giuliano, Claudio ;
Ercolani, Caterina ;
Narjes, Frank ;
Koch, Uwe ;
Rowley, Michael ;
Altamura, Sergio ;
De Francesco, Raffaele ;
Neddermann, Petra ;
Migliaccio, Giovanni ;
Stansfield, Ian .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2009, 19 (06) :1779-1783