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Dipyridodiazepinone derivatives; synthesis and anti HIV-1 activity

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dc.contributor.authorNisachon Khunnawutmanothamen_US
dc.contributor.authorNitirat Chimnoien_US
dc.contributor.authorArunee Thitithanyanonten_US
dc.contributor.authorPatchreenart Saparpakornen_US
dc.contributor.authorKiattawee Choowongkomonen_US
dc.contributor.authorPornpan Pungpoen_US
dc.contributor.authorSupa Hannongbuaen_US
dc.contributor.authorSupanna Techasakulen_US
dc.contributor.otherChulabhorn Research Instituteen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherKasetsart Universityen_US
dc.contributor.otherUbon Rajathanee Universityen_US
dc.date.accessioned2018-09-13T06:31:08Z
dc.date.available2018-09-13T06:31:08Z
dc.date.issued2009-07-22en_US
dc.description.abstractTen dipyridodiazepinone derivatives were synthesized and evaluated for their anti HIV-1 reverse transcriptase activity against wildtype and mutant type enzymes, K103N and Y181C. Two of them were found to be promising inhibitors for HIV-1 RT. © 2009 Khunnawutmanotham et al; licensee Beilstein-Institut.en_US
dc.identifier.citationBeilstein Journal of Organic Chemistry. Vol.5, (2009)en_US
dc.identifier.doi10.3762/bjoc.5.36en_US
dc.identifier.issn18605397en_US
dc.identifier.issn18605397en_US
dc.identifier.other2-s2.0-75949110371en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/27411
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=75949110371&origin=inwarden_US
dc.subjectChemistryen_US
dc.titleDipyridodiazepinone derivatives; synthesis and anti HIV-1 activityen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=75949110371&origin=inwarden_US

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