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- W2403369691 endingPage "864" @default.
- W2403369691 startingPage "847" @default.
- W2403369691 abstract "Reverse transcriptase (RT) is a multifunctional enzyme in the human immunodeficiency virus (HIV)-1 life cycle and represents a primary target for drug discovery efforts against HIV-1 infection. Two classes of RT inhibitors, the nucleoside RT inhibitors (NRTIs) and the nonnucleoside transcriptase inhibitors are prominently used in the highly active antiretroviral therapy in combination with other anti-HIV drugs. However, the rapid emergence of drug-resistant viral strains has limited the successful rate of the anti-HIV agents. Computational methods are a significant part of the drug design process and indispensable to study drug resistance. In this review, recent advances in computer-aided drug design for the rational design of new compounds against HIV-1 RT using methods such as molecular docking, molecular dynamics, free energy calculations, quantitative structure-activity relationships, pharmacophore modelling and absorption, distribution, metabolism, excretion and toxicity prediction are discussed. Successful applications of these methodologies are also highlighted." @default.
- W2403369691 created "2016-06-24" @default.
- W2403369691 creator A5018426427 @default.
- W2403369691 creator A5054175906 @default.
- W2403369691 creator A5057144159 @default.
- W2403369691 date "2015-11-01" @default.
- W2403369691 modified "2023-09-27" @default.
- W2403369691 title "Computational drug design strategies applied to the modelling of human immunodeficiency virus-1 reverse transcriptase inhibitors" @default.
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