SYNTHESIS OF ACETAMIDOSULFONAMIDE DERIVATIVES WITH ANTIOXIDATIVE AND QSAR STUDIES

dc.contributor.authorWorachartcheewan A.
dc.contributor.authorPisutjaroenpong S.
dc.contributor.authorPingaew R.
dc.contributor.authorPrachayasittikul S.
dc.contributor.authorSiriwong S.
dc.contributor.authorRuchirawat S.
dc.contributor.authorPrachayasittikul V.
dc.contributor.otherMahidol University
dc.date.accessioned2023-06-18T16:49:34Z
dc.date.available2023-06-18T16:49:34Z
dc.date.issued2022-01-03
dc.description.abstractA series of sixteen acetamidosulfonamide derivatives (1-16) have been synthesized and investigated for their antioxidant (radical scavenging and superoxide dismutase (SOD)) and antimicrobial activities. Most compounds exhibited antioxidant activities in which compound 15 displayed the most potent radical scavenging and SOD activities. Quantitative structure-activity relationship (QSAR) has been studied using multiple linear regression. 2 The constructed QSAR models displayed high correlation coefficient (QLOO- = 0.9708 and 0.8753 for RSA CV and SOD activities, respectively), but low root mean square error (RMSELOO-CV = 0.5105 and 1.3571 for RSA and SOD activities, respectively). The structure-activity relationship showed that an ethylene group connected to pyridine ring provided significant antioxidant activities. The QSAR models give insight into the rational designed of eighty new sulfonamides with various electron donating and withdrawing groups. The top five new designed sulfonamides with nitro group are potential antioxidants to be further developed for medicinal applications.
dc.identifier.citationEXCLI Journal Vol.21 (2022) , 360-379
dc.identifier.doi10.17179/excli2021-4590
dc.identifier.eissn16112156
dc.identifier.scopus2-s2.0-85127639321
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/83862
dc.rights.holderSCOPUS
dc.subjectBiochemistry, Genetics and Molecular Biology
dc.titleSYNTHESIS OF ACETAMIDOSULFONAMIDE DERIVATIVES WITH ANTIOXIDATIVE AND QSAR STUDIES
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85127639321&origin=inward
oaire.citation.endPage379
oaire.citation.startPage360
oaire.citation.titleEXCLI Journal
oaire.citation.volume21
oairecerif.author.affiliationLaboratory of Medicinal Chemistry
oairecerif.author.affiliationChulabhorn Graduate Institute
oairecerif.author.affiliationMahidol University
oairecerif.author.affiliationSrinakharinwirot University
oairecerif.author.affiliationMinistry of Education

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