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Aurocitrin and related polyketide metabolites from the wood-decay fungus Hypocrea sp. BCC 14122

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dc.contributor.authorPitchapa Berkaewen_US
dc.contributor.authorNoppamas Soonthornchareonnonen_US
dc.contributor.authorKitlada Salasawadeeen_US
dc.contributor.authorRungtiwa Chanthaketen_US
dc.contributor.authorMasahiko Isakaen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherThailand National Center for Genetic Engineering and Biotechnologyen_US
dc.contributor.otherNational Center for Genetic Engineering and Biotechnologyen_US
dc.date.accessioned2018-07-12T02:18:58Z
dc.date.available2018-07-12T02:18:58Z
dc.date.issued2008-05-01en_US
dc.description.abstractThe known gentisaldehyde antibiotic aurocitrin (1), its cis-olefinic isomer (2), a salicylaldehyde analogue (3), two new benzofuran derivatives (4 and 5), and a new dihydroisocoumarin (6) were isolated from the wood-decay fungus Hypocrea sp. BCC 14122. The structures were elucidated primarily by NMR and mass spectroscopic analyses. © 2008 American Chemical Society and American Society of Pharmacognosy.en_US
dc.identifier.citationJournal of Natural Products. Vol.71, No.5 (2008), 902-904en_US
dc.identifier.doi10.1021/np700740aen_US
dc.identifier.issn01633864en_US
dc.identifier.other2-s2.0-45249117900en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/18932
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=45249117900&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectMedicineen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleAurocitrin and related polyketide metabolites from the wood-decay fungus Hypocrea sp. BCC 14122en_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=45249117900&origin=inwarden_US

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