Publication:
Synthesis, in vitro evaluation, and docking studies of novel chromone derivatives as HIV-1 protease inhibitor

dc.contributor.authorJiraporn Ungwitayatornen_US
dc.contributor.authorChanpen Wiwaten_US
dc.contributor.authorWeerasak Sameeen_US
dc.contributor.authorPatcharawee Nunthanavaniten_US
dc.contributor.authorNarumol Phosrithongen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherSrinakharinwirot Universityen_US
dc.contributor.otherSiam Universityen_US
dc.date.accessioned2018-05-03T08:07:00Z
dc.date.available2018-05-03T08:07:00Z
dc.date.issued2011-08-24en_US
dc.description.abstractNovel chromone derivatives with a benzopyran-4-one scaffold have been prepared by the one-pot cyclization reaction. The in vitro inhibitory activity of these new compounds towards HIV-1 protease have been evaluated using stop time HPLC method as the preliminary screening. The most potent compound, 7,8-dihydroxy-2-(3′-trifluoromethyl phenyl)-3-(3″- trifluoromethylbenzoyl)chromone (32), showed IC 50 = 0.34 μM. The molecular docking study supported results from experimental activity testing and also provided structure-activity relationship of this series. © 2011 Elsevier B.V. All rights reserved.en_US
dc.identifier.citationJournal of Molecular Structure. Vol.1001, No.1-3 (2011), 152-161en_US
dc.identifier.doi10.1016/j.molstruc.2011.06.035en_US
dc.identifier.issn00222860en_US
dc.identifier.other2-s2.0-79961032360en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/11702
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79961032360&origin=inwarden_US
dc.subjectChemistryen_US
dc.titleSynthesis, in vitro evaluation, and docking studies of novel chromone derivatives as HIV-1 protease inhibitoren_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79961032360&origin=inwarden_US

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