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Antimalarial sesquiterpenes from tubers of Cyperus rotundus: structure of 10,12-Peroxycalamenene, a sesquiterpene endoperoxide

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dc.contributor.authorC. Thebtaranonthen_US
dc.contributor.authorY. Thebtaranonthen_US
dc.contributor.authorS. Wanauppathamkulen_US
dc.contributor.authorY. Yuthavongen_US
dc.contributor.otherThailand National Science and Technology Development Agencyen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherThailand National Center for Genetic Engineering and Biotechnologyen_US
dc.date.accessioned2018-07-04T06:52:02Z
dc.date.available2018-07-04T06:52:02Z
dc.date.issued1995-01-01en_US
dc.description.abstractActivity-guided investigation of Cyperus rotundus tubers led to the isolation of patchoulenone, caryophyllene α-oxide, 10,12-peroxycalamenene and 4,7-dimethyl-1-tetralone. The antimalarial activities of these compounds are in the range of EC5010-4-10-6M, with the novel endoperoxide sesquiterpene, 10,12-peroxycalamenene, exhibiting the strongest effect at EC502.33 × 10-6M. © 1995.en_US
dc.identifier.citationPhytochemistry. Vol.40, No.1 (1995), 125-128en_US
dc.identifier.doi10.1016/0031-9422(95)00260-Een_US
dc.identifier.issn00319422en_US
dc.identifier.other2-s2.0-0029360451en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/17232
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0029360451&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleAntimalarial sesquiterpenes from tubers of Cyperus rotundus: structure of 10,12-Peroxycalamenene, a sesquiterpene endoperoxideen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0029360451&origin=inwarden_US

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