Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14787
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dc.contributor.authorPrachayasittikul S.
dc.contributor.authorLimnusont P.
dc.contributor.authorPingaew R.
dc.contributor.authorRuchirawat S.
dc.contributor.authorPrachayasittikul V.
dc.date.accessioned2021-04-05T04:31:56Z-
dc.date.available2021-04-05T04:31:56Z-
dc.date.issued2009
dc.identifier.issn16112156
dc.identifier.other2-s2.0-70349926076
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/14787-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-70349926076&partnerID=40&md5=298b3664f09112e729d13e7c315dcd3b
dc.description.abstractAn array of interesting activities for bioactive 3-substituted thiopyridines have previously been reported. Herein, a series of α-and β-(1-adamantylthio) analogs of 3-picoline and phenylpyridines were prepared and investigated for antimicrobial (agar dilution method against 21 strains of microorganisms) and antimalarial (against P. falciparum) activities. It was found that β-thiopyridines, 5-(1-adamantylthio)-3-picoline (7) and 3-(1-adamantylthio)-4-phenylpyridine (8) are novel antimicrobials and antimalarials. Significantly, analogs 7 and 8 are very potent antimicrobials with MIC range of 2-32 μg/mL where 8 being the most potent. The β-sulfides 7 and 8 selectively inhibited the growth of tested gram-positive bacteria, but inactive against gram-negative bacilli including the members of Enterobacteriaceae. This study identified new antimicrobials that represent promising lead compounds suitable for further preclinical and clinical development.
dc.titleβ-(1-Adamantylthio)pyridine analogs as antimicrobials and antimalarials
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationEXCLI Journal. Vol 8, No. (2009), p.35-40
Appears in Collections:Scopus 1983-2021

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