Abstract |
The search for a cure for hepatitis B virus infection extends beyond interferon and the existing polymerase inhibitors, and targets different aspects of the virus life cycle to develop agents that operate by alternative mechanisms. Examples of small molecules that disrupt the encapsidation of pgRNA have been known for some time, but recent advances in the understanding of nucleocapsid formation, how compounds interact with core protein, and the development of drug-like molecules have recently progressed the study of capsid assembly modulators to proof of concept in the clinic with respect to reduction of viral load in chronic HBV patients. Interference with HBV capsid assembly is thus a legitimate approach to treating HBV infection.
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Authors | Andrew G Cole |
Journal | Current opinion in pharmacology
(Curr Opin Pharmacol)
Vol. 30
Pg. 131-137
(10 2016)
ISSN: 1471-4973 [Electronic] England |
PMID | 27636324
(Publication Type: Journal Article, Review)
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Copyright | Copyright © 2016 Elsevier Ltd. All rights reserved. |
Chemical References |
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Topics |
- Animals
- Antiviral Agents
(pharmacology)
- Capsid
(drug effects)
- Drug Design
- Hepatitis B virus
(drug effects)
- Hepatitis B, Chronic
(drug therapy, virology)
- Humans
- Viral Load
(drug effects)
- Virus Assembly
(drug effects)
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