HIV-1 RT-Associated RNase H Function Inhibitors: Recent Advances in Drug Development

Author(s): E. Tramontano, R. Di Santo.

Journal Name:Current Medicinal Chemistry

Volume 17 , Issue 26 , 2010

Abstract:

The HIV-1 genomic RNA reverse transcription is an essential step in the virus cycle carried out by the viral-coded reverse transcriptase (RT), which has two associated functions: the RNA- and DNA-dependent DNA polymerase (RDDP and DDDP) function and the ribonuclease H (RNase H) function. The RNase H function catalyzes the selective hydrolysis of the RNA strand of the RNA:DNA heteroduplex replication intermediate. The RT associated activities are both essential for HIV-1 replication and validated targets for drug development, but only the polymerase function has been widely investigated as drug target. In fact, either nucleoside or non-nucleoside RT inhibitors currently used in therapy act on the polymerase associated activity. In this review, we describe the compounds, reported up to today, which inhibit the HIV-1 RNase H function, their chemical structures, the structure-activity relationships and the mechanism of action.

Keywords: HIV-1, reverse transcriptase, ribonuclease H, RNase H, RNase H inhibitor, natural compounds, diketo acids, hydrazones

Rights & PermissionsPrintExport

Article Details

VOLUME: 17
ISSUE: 26
Year: 2010
Page: [2837 - 2853]
Pages: 17
DOI: 10.2174/092986710792065045
Price: $58

Article Metrics

PDF: 12
HTML: 0
EPUB: 0
PRC: 0