Publication:
A new sulfoxide analog of 1,2,3,6-tetrahydrophenylpyridine and antimicrobial activity

dc.contributor.authorSupaluk Prachayasittikulen_US
dc.contributor.authorRatchanok Pingaewen_US
dc.contributor.authorApilak Worachartcheewanen_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.date.accessioned2018-09-24T08:37:02Z
dc.date.available2018-09-24T08:37:02Z
dc.date.issued2010-12-01en_US
dc.description.abstractBioactivities of thiotetrahydropyridines were previously described. Herein, a novel bioactive sulfoxide analog; N-acetyl-2-(1-adamantylsulfoxo)-3-acetoxy-4-phenyl-6-hydroxy-1,2,3,6-tet rahydropyridine (3) from the deoxydative substitution of 4-phenylpyridine 1-oxide is reported. Its structure was elucidated using spectral data including 2D-NMR, MS, IR and UV. The sulfoxide 3 exhibited antibacterial activity against Moraxella catarrhalis and Streptococcus pyogenes with minimum inhibitory concentration of 128 and 256 μg/mL, respectively.en_US
dc.identifier.citationEXCLI Journal. Vol.9, (2010), 102-107en_US
dc.identifier.issn16112156en_US
dc.identifier.other2-s2.0-79151486711en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/28428
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79151486711&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleA new sulfoxide analog of 1,2,3,6-tetrahydrophenylpyridine and antimicrobial activityen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79151486711&origin=inwarden_US

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