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Discovery and Development of Anti-HBV Agents and Their Resistance

Hepatitis B virus (HBV) infection is a prime cause of liver diseases such as hepatitis, cirrhosis and hepatocellular carcinoma. The current drugs clinically available are nucleot(s)ide analogues that inhibit viral reverse transcriptase activity. Most drugs of this class are reported to have viral re...

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Autores principales: Kim, Kyun-Hwan, Kim, Nam Doo, Seong, Baik-Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257723/
https://www.ncbi.nlm.nih.gov/pubmed/20802402
http://dx.doi.org/10.3390/molecules15095878
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author Kim, Kyun-Hwan
Kim, Nam Doo
Seong, Baik-Lin
author_facet Kim, Kyun-Hwan
Kim, Nam Doo
Seong, Baik-Lin
author_sort Kim, Kyun-Hwan
collection PubMed
description Hepatitis B virus (HBV) infection is a prime cause of liver diseases such as hepatitis, cirrhosis and hepatocellular carcinoma. The current drugs clinically available are nucleot(s)ide analogues that inhibit viral reverse transcriptase activity. Most drugs of this class are reported to have viral resistance with breakthrough. Recent advances in methods for in silico virtual screening of chemical libraries, together with a better understanding of the resistance mechanisms of existing drugs have expedited the discovery and development of novel anti-viral drugs. This review summarizes the current status of knowledge about and viral resistance of HBV drugs, approaches for the development of novel drugs as well as new viral and host targets for future drugs.
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spelling pubmed-62577232018-12-06 Discovery and Development of Anti-HBV Agents and Their Resistance Kim, Kyun-Hwan Kim, Nam Doo Seong, Baik-Lin Molecules Review Hepatitis B virus (HBV) infection is a prime cause of liver diseases such as hepatitis, cirrhosis and hepatocellular carcinoma. The current drugs clinically available are nucleot(s)ide analogues that inhibit viral reverse transcriptase activity. Most drugs of this class are reported to have viral resistance with breakthrough. Recent advances in methods for in silico virtual screening of chemical libraries, together with a better understanding of the resistance mechanisms of existing drugs have expedited the discovery and development of novel anti-viral drugs. This review summarizes the current status of knowledge about and viral resistance of HBV drugs, approaches for the development of novel drugs as well as new viral and host targets for future drugs. MDPI 2010-08-27 /pmc/articles/PMC6257723/ /pubmed/20802402 http://dx.doi.org/10.3390/molecules15095878 Text en © 2010 by the authors; http://creativecommons.org/licenses/by/3.0/ licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Kim, Kyun-Hwan
Kim, Nam Doo
Seong, Baik-Lin
Discovery and Development of Anti-HBV Agents and Their Resistance
title Discovery and Development of Anti-HBV Agents and Their Resistance
title_full Discovery and Development of Anti-HBV Agents and Their Resistance
title_fullStr Discovery and Development of Anti-HBV Agents and Their Resistance
title_full_unstemmed Discovery and Development of Anti-HBV Agents and Their Resistance
title_short Discovery and Development of Anti-HBV Agents and Their Resistance
title_sort discovery and development of anti-hbv agents and their resistance
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257723/
https://www.ncbi.nlm.nih.gov/pubmed/20802402
http://dx.doi.org/10.3390/molecules15095878
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