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dc.contributor.authorRatchanok Pingaewen_US
dc.contributor.authorVeda Prachayasittikulen_US
dc.contributor.authorApilak Worachartcheewanen_US
dc.contributor.authorChanin Nantasenamaten_US
dc.contributor.authorSupaluk Prachayasittikulen_US
dc.contributor.authorSomsak Ruchirawaten_US
dc.contributor.authorVirapong Prachayasittikulen_US
dc.contributor.otherSrinakharinwirot Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherChulabhorn Research Instituteen_US
dc.contributor.otherMinistry of Educationen_US
dc.date.accessioned2018-11-23T09:55:41Z-
dc.date.available2018-11-23T09:55:41Z-
dc.date.issued2015-10-20en_US
dc.identifier.citationEuropean Journal of Medicinal Chemistry. Vol.103, (2015), 446-459en_US
dc.identifier.issn17683254en_US
dc.identifier.issn02235234en_US
dc.identifier.other2-s2.0-84942155183en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84942155183&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/35732-
dc.description.abstract© 2015 Elsevier Masson SAS. A novel series of 1,4-naphthoquinones (33-44) tethered by open and closed chain sulfonamide moieties were designed, synthesized and evaluated for their cytotoxic and antimalarial activities. All quinone-sulfonamide derivatives displayed a broad spectrum of cytotoxic activities against all of the tested cancer cell lines including HuCCA-1, HepG2, A549 and MOLT-3. Most quinones (33-36 and 38-43) exerted higher anticancer activity against HepG2 cell than that of the etoposide. The open chain analogs 36 and 42 were shown to be the most potent compounds. Notably, the restricted sulfonamide analog 38 with 6,7-dimethoxy groups exhibited the most potent antimalarial activity (IC<inf>50</inf> = 2.8 μM). Quantitative structure-activity relationships (QSAR) study was performed to reveal important chemical features governing the biological activities. Five constructed QSAR models provided acceptable predictive performance (R<inf>cv</inf> 0.5647-0.9317 and RMSE<inf>cv</inf> 0.1231-0.2825). Four additional sets of structurally modified compounds were generated in silico (34a-34d, 36a-36k, 40a-40d and 42a-42k) in which their activities were predicted using the constructed QSAR models. A comprehensive discussion of the structure-activity relationships was made and a set of promising compounds (i.e., 33, 36, 38, 42, 36d, 36f, 42e, 42g and 42f) was suggested for further development as anticancer and antimalarial agents.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84942155183&origin=inwarden_US
dc.subjectChemistryen_US
dc.titleNovel 1,4-naphthoquinone-based sulfonamides: Synthesis, QSAR, anticancer and antimalarial studiesen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1016/j.ejmech.2015.09.001en_US
Appears in Collections:Scopus 2011-2015

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