Literature DB >> 20001555

Investigational drugs for hepatitis C.

Robert Flisiak1, Anna Parfieniuk.   

Abstract

IMPORTANCE OF THE FIELD: Hepatitis C virus (HCV) infection affects 180 million people worldwide. Standard anti-HCV therapy combines effect of pegylated IFN-alpha on immune response and antiviral activity of ribavirin. Sustained virological response rate achieved with this standard of care medication is around 50% for HCV genotype 1, the most prevalent worldwide genotype. So there is an obvious need to enhance efficacy of treatment. AREAS COVERED IN THIS REVIEW: We describe novel treatment options studied within the recent few years, which are focused on inhibitors of HCV-specific enzymes such as NS3/4 protease and NS5B polymerase or influence host-virus interactions. WHAT THE READER WILL GAIN: According to the most recent data, triple therapies consisted of pegylated interferons, ribavirin and protease inhibitors demonstrate significant improvement of treatment efficacy in comparison to current standard of care medication. Moreover, new forms of interferons and ribavirin, more effective, less toxic, and more convenient, become probably a fundamental component of anti-HCV therapy in the near future. TAKE HOME MESSAGE: In coming years, we can expect that triple therapy becomes a standard medication, and treatment without interferon and/or ribavirin becomes a new studied therapeutic scenario.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20001555     DOI: 10.1517/13543780903431034

Source DB:  PubMed          Journal:  Expert Opin Investig Drugs        ISSN: 1354-3784            Impact factor:   6.206


  5 in total

1.  Interactions of ketoamide inhibitors on HCV NS3/4A protease target: molecular docking studies.

Authors:  Abdul Wadood; Muhammad Riaz; Syed Babar Jamal; Masaud Shah
Journal:  Mol Biol Rep       Date:  2014-01       Impact factor: 2.316

2.  Inhibitors of the Hepatitis C Virus RNA-Dependent RNA Polymerase NS5B.

Authors:  Megan H Powdrill; Jean A Bernatchez; Matthias Götte
Journal:  Viruses       Date:  2010-09-28       Impact factor: 5.818

3.  A cell-based assay for RNA synthesis by the HCV polymerase reveals new insights on mechanism of polymerase inhibitors and modulation by NS5A.

Authors:  C T Ranjith-Kumar; Yahong Wen; Nielson Baxter; Kanchan Bhardwaj; C Cheng Kao
Journal:  PLoS One       Date:  2011-07-22       Impact factor: 3.240

4.  Optimization of Benzoisothiazole dioxide inhibitory activity of the NS5B polymerase of HCV genotype 4 using ligand-steered homological modeling, reaction-driven scaffold-hopping and Enovo workflow.

Authors:  Amr Hamed Mahmoud; Khaled Abouzid Mohamed Abouzid; Dalal Abd El Rahman Abou El Ella; Mohamed Abdel Hamid Ismail
Journal:  Bioinformation       Date:  2011-12-10

5.  In silico identification and evaluation of leads for the simultaneous inhibition of protease and helicase activities of HCV NS3/4A protease using complex based pharmacophore mapping and virtual screening.

Authors:  Abdul Wadood; Muhammad Riaz; Reaz Uddin; Zaheer Ul-Haq
Journal:  PLoS One       Date:  2014-02-13       Impact factor: 3.240

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.