| Literature DB >> 28088905 |
Xueshun Wang1, Ping Gao1, Luis Menendez-Arias2, Xinyong Liu1, Peng Zhan1.
Abstract
Combinations of antiretroviral drugs are successfully used to treat HIV-infected patients. However, drug resistance is a major problem that makes discovery of new antiretroviral drugs an ongoing priority. The ribonuclease H (RNase H) activity of the HIV-1 reverse transcriptase catalyzes the selective hydrolysis of the RNA strand of RNA:DNA heteroduplex replication intermediates, and represents an attractive unexploited target for drug development. This review reports on recent progress in the characterization of HIV-1 RNase H inhibitors from 2013 to 2016, describing their chemical structures, structureactivity relationship and binding modes. Focus is given to emerging medicinal chemistry principles and insights into the discovery and development of RNase H inhibitors. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.Entities:
Keywords: AIDS; HIV-1; RNase H inhibitors; SAR; antiviral; drug design; dual inhibitors; metalloenzyme.
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Year: 2018 PMID: 28088905 DOI: 10.2174/0929867324666170113110839
Source DB: PubMed Journal: Curr Med Chem ISSN: 0929-8673 Impact factor: 4.530