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What do docking and QSAR tell us about the design of HIV-1 reverse transcriptase nonnucleoside inhibitors?


ABSTRACT: Despite vigorous studies, effective nonnucleoside inhibitors of HIV-1 reverse transcriptase (NNRTIs) are still in demand, not only due to toxicity and detrimental side effects of currently used drugs but also because of the emergence of multidrug-resistant viral strains. In this contribution, we present results of docking of 47 inhibitors to 107 allosteric centers of HIV-1 reverse transcriptase. Based on the average binding scores, we have constructed QSAR equations to elucidate directions of further developments in the inhibitor design that come from this structural data.

SUBMITTER: Paneth A 

PROVIDER: S-EPMC5655543 | biostudies-literature | 2017 Oct

REPOSITORIES: biostudies-literature

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What do docking and QSAR tell us about the design of HIV-1 reverse transcriptase nonnucleoside inhibitors?

Paneth Agata A   Płonka Wojciech W   Paneth Piotr P  

Journal of molecular modeling 20171019 11


Despite vigorous studies, effective nonnucleoside inhibitors of HIV-1 reverse transcriptase (NNRTIs) are still in demand, not only due to toxicity and detrimental side effects of currently used drugs but also because of the emergence of multidrug-resistant viral strains. In this contribution, we present results of docking of 47 inhibitors to 107 allosteric centers of HIV-1 reverse transcriptase. Based on the average binding scores, we have constructed QSAR equations to elucidate directions of fu  ...[more]

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