Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/725
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dc.contributor.authorPrabhakar, Yenamandra S-
dc.date.accessioned2016-04-04T07:36:43Z-
dc.date.available2016-04-04T07:36:43Z-
dc.date.issued2015-11-
dc.identifier.urihttp://hdl.handle.net/123456789/725-
dc.description.abstractIn a focused exploration, thiazolidin-4-ones with different C-2 and N-3 substituent groups were synthesized and evaluated as non-nucleoside reverse transcriptase inhibitors against HIV-1. This has led to new active compounds sporting heteroaryls at both C-2 and N-3 positions prompting to view them in the backdrop of nevirapine. To assign the molecular attributes for the activity, the compounds are investigated by docking them into non-nucleoside inhibitor-binding pocket of HIV-1 reverse transcriptase (RT). The most active compounds of this series (7d and 7f) shared spatial features with nevirapine with added molecular flexibility. Furthermore, in molecular dynamics simulations carried out for up to 10 ns, the compounds 7d and 7f showed consistency in their interactions with non-nucleoside inhibitor-binding pocket of HIV-1 RT and suggested Tyr319 and Val106 as potential residues for H-bond interaction with these molecules. These results open new avenues for the exploration of 2,3-diheteroaryl thiazolidin-4-ones for prevention of HIV-1.en_US
dc.publisherJohn Wiley & Sons A/Sen_US
dc.titleSynthesis, Biological Evaluation and Molecular Modeling Studies of New 2,3-Diheteroaryl Thiazolidin-4- Ones as NNRTIsen_US
dc.contributor.coauthorDebnath, Utsab-
dc.contributor.coauthorVerma, Saroj-
dc.contributor.coauthorSingh, Pankaj-
dc.contributor.coauthorRawat, Kavita-
dc.contributor.coauthorGupta, Satish Kumar-
dc.contributor.coauthorTripathi, Raj K-
dc.contributor.coauthorSiddiqui, Hefazat H-
dc.contributor.coauthorKatti, Seturam B-
dc.journalChemical Biology & Drug Designen_US
dc.volumeno86en_US
dc.issueno5en_US
dc.pages1285-1291en_US
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