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- W3082959030 endingPage "926" @default.
- W3082959030 startingPage "918" @default.
- W3082959030 abstract "The importance of new effective treatment methodologies for human immunodeficiency virus (HIV) is undeniable for the medical society. Viral protein U (Vpu), one of the disparaged accessory proteins of HIV, is responsible for the dissemination of viral particles, and HIV mutants lacking Vpu protein have remarkably reduced pathogenicity. Here, we explored the marine natural products to find the leading structures which can potentially inhibit the activity of Vpu in silico. To fulfill this goal, we set up a virtual screening based on molecular docking to evaluate the binding capacity of different marine products to Vpu. For validation, we used molecular dynamics simulation and monitored the root mean square deviation value and binding interactions. The results were intriguing when we realized that the hit compounds (phlorotannins) had previously been identified as reverse transcriptase and HIV protease inhibitors. This research inaugurates a new road to combat HIV by multifaceted mode of action of these marine natural products without putting the normal cells in jeopardy (with their safe toxicological profile)." @default.
- W3082959030 created "2020-09-08" @default.
- W3082959030 creator A5001453149 @default.
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- W3082959030 date "2020-09-18" @default.
- W3082959030 modified "2023-10-17" @default.
- W3082959030 title "Phlorotannins as HIV Vpu inhibitors, an <i>in silico</i> virtual screening study of marine natural products" @default.
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- W3082959030 doi "https://doi.org/10.1002/bab.2014" @default.
- W3082959030 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/32860447" @default.
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