Literature DB >> 21942423

Novel therapies for hepatitis C: insights from the structure of the virus.

Dahlene N Fusco1, Raymond T Chung.   

Abstract

For the first time since the discovery of the hepatitis C virus (HCV), therapeutic options for hepatitis C have expanded. Several agents directly effective against HCV are now in development, including both direct-acting antiviral agents (DAAs) and host cofactor inhibitors. DAAs have been developed to inhibit several HCV proteins, including the NS3/4A serine protease, the NS5B RNA polymerase, NS5A, and NS4B. Host cofactor inhibitors include, but are not limited to, cyclophilin inhibitors, miR122 antagonists, and statins. Development of these agents represents a major advance in HCV therapeutics. This review provides a guide to HCV drugs in various stages of development, including an introduction to their mechanism of action, state of clinical development, efficacy, and side effects.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21942423     DOI: 10.1146/annurev-med-042010-085715

Source DB:  PubMed          Journal:  Annu Rev Med        ISSN: 0066-4219            Impact factor:   13.739


  18 in total

1.  SOCS1 abrogates IFN's antiviral effect on hepatitis C virus replication.

Authors:  Run-Xuan Shao; Leiliang Zhang; Zhi Hong; Kaku Goto; Du Cheng; Wen-Chi Chen; Nikolaus Jilg; Kattareeya Kumthip; Dahlene N Fusco; Lee F Peng; Raymond T Chung
Journal:  Antiviral Res       Date:  2012-12-10       Impact factor: 5.970

2.  Modeling quasispecies and drug resistance in hepatitis C patients treated with a protease inhibitor.

Authors:  Libin Rong; Ruy M Ribeiro; Alan S Perelson
Journal:  Bull Math Biol       Date:  2012-05-26       Impact factor: 1.758

3.  Structure-activity relationship studies on quinoxalin-2(1H)-one derivatives containing thiazol-2-amine against hepatitis C virus leading to the discovery of BH6870.

Authors:  Qi-Fei Zhong; Rui Liu; Gang Liu
Journal:  Mol Divers       Date:  2015-07-24       Impact factor: 2.943

4.  Fast hepatitis C virus RNA elimination and NS5A redistribution by NS5A inhibitors studied by a multiplex assay approach.

Authors:  Dandan Liu; Juan Ji; Tanya P Ndongwe; Eleftherios Michailidis; Charles M Rice; Robert Ralston; Stefan G Sarafianos
Journal:  Antimicrob Agents Chemother       Date:  2015-04-06       Impact factor: 5.191

5.  In Silico Drug Discovery for Treatment of Virus Diseases.

Authors:  Shikha Joon; Rajeev K Singla; Bairong Shen
Journal:  Adv Exp Med Biol       Date:  2022       Impact factor: 2.622

6.  Mathematical analysis of multiscale models for hepatitis C virus dynamics under therapy with direct-acting antiviral agents.

Authors:  Libin Rong; Alan S Perelson
Journal:  Math Biosci       Date:  2013-05-16       Impact factor: 2.144

7.  Combination of pharmacophore hypothesis and molecular docking to identify novel inhibitors of HCV NS5B polymerase.

Authors:  Amaravadhi Harikishore; Enlin Li; Jia Jun Lee; Nam-Joon Cho; Ho Sup Yoon
Journal:  Mol Divers       Date:  2015-04-11       Impact factor: 2.943

8.  Unconventional miR-122 binding stabilizes the HCV genome by forming a trimolecular RNA structure.

Authors:  Stefanie A Mortimer; Jennifer A Doudna
Journal:  Nucleic Acids Res       Date:  2013-02-14       Impact factor: 16.971

Review 9.  Cyclophilin inhibitors: an emerging class of therapeutics for the treatment of chronic hepatitis C infection.

Authors:  Sam Hopkins; Philippe Gallay
Journal:  Viruses       Date:  2012-10-29       Impact factor: 5.048

10.  Analysis of hepatitis C virus decline during treatment with the protease inhibitor danoprevir using a multiscale model.

Authors:  Libin Rong; Jeremie Guedj; Harel Dahari; Daniel J Coffield; Micha Levi; Patrick Smith; Alan S Perelson
Journal:  PLoS Comput Biol       Date:  2013-03-14       Impact factor: 4.475

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.