Design and Development of Anti-Hepatitis B Virus Agents

Author(s): S. Kaushik, S. P. Gupta, P. K. Sharma.

Journal Name: Current Medicinal Chemistry

Volume 17 , Issue 29 , 2010

Submit Manuscript
Submit Proposal

Abstract:

Hepatitis B virus (HBV) infected hepatitis is the common infectious disease. In the World Conservative Estimate Plan, the number of persons chronically infected with HBV is more than 300 million. Current regimen of treatment is far from satisfactory, as it is associated with certain side effects and viral resistance capacity. Therefore, a serious attention has recently been paid to the design and development of new potent anti-HBV agents. A variety of drugs have been synthesized and screened for their anti-HBV effects. These include nucleosides, natural compounds, quinolines, benzodiazepines, indoles, etc. Many of them are in wide trend in current treatment regimen. In this review, we have presented the recent development on the design and development of all categories of HBV inhibitors studied.

Keywords: Anti-hepatitis B virus agents, nucleosides, quinolines, benzodiazepines, indoles, Anti-Hepatitis B, Virus, (HBV), STERIMOL parameter, surface antigen, nucleocapsid core antigen, pre-core antigen, HBV replication, DNA polymerase, DNA, RNA, Chronic Hepatitis, Active prophylaxis, Passive Immunization, Interferon, Immunomodulators, Adoptive Immune Transfer, Nucleoside Analogs, thrombocytopenia, anemia, DHBV, famciclovir, Sophora flavescens, X-ray analysis, Hypserpa nitida, Alisma orientalis, replication, Inhi-bition assay, BENZODIAZEPINESINDOL, lamivudine, (QSAR)

Rights & PermissionsPrintExport Cite as


Article Details

VOLUME: 17
ISSUE: 29
Year: 2010
Page: [3377 - 3392]
Pages: 16
DOI: 10.2174/092986710793176375
Price: $58

Article Metrics

PDF: 6