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2-Substituted furans from Polyalthia suberosa

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dc.contributor.authorP. Tuchindaen_US
dc.contributor.authorM. Pohmakotren_US
dc.contributor.authorV. Reutrakulen_US
dc.contributor.authorW. Thanyachareonen_US
dc.contributor.authorS. Sophasanen_US
dc.contributor.authorC. Yoosooken_US
dc.contributor.authorT. Santisuken_US
dc.contributor.authorJ. M. Pezzutoen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherThailand Royal Forest Departmenten_US
dc.contributor.otherUniversity of Illinois at Chicagoen_US
dc.date.accessioned2018-09-07T09:37:41Z
dc.date.available2018-09-07T09:37:41Z
dc.date.issued2001-09-11en_US
dc.description.abstractTwo new 2-substituted furans, 1-(2-furyl)pentacosa-16,18-diyne and 23-(2-furyl)tricosa-5,7-diynoic acid, have been isolated from stems of Polyalthia suberosa. The structures were assigned by spectroscopic methods. The two compounds together with the previously reported kalasinamide, N-trans-feruloyltyramine and N-trans-coumaroyltyramine showed anti-HIV activities.en_US
dc.identifier.citationPlanta Medica. Vol.67, No.6 (2001), 572-575en_US
dc.identifier.doi10.1055/s-2001-16469en_US
dc.identifier.issn00320943en_US
dc.identifier.other2-s2.0-0034860812en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/26448
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0034860812&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectMedicineen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.title2-Substituted furans from Polyalthia suberosaen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0034860812&origin=inwarden_US

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