Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/52194
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dc.contributor.authorMariko Kitajimaen_US
dc.contributor.authorSatoko Oharaen_US
dc.contributor.authorNoriyuki Kogureen_US
dc.contributor.authorDammrong Santiarwornen_US
dc.contributor.authorHiromitsu Takayamaen_US
dc.date.accessioned2018-09-04T09:21:58Z-
dc.date.available2018-09-04T09:21:58Z-
dc.date.issued2013-11-11en_US
dc.identifier.issn14645416en_US
dc.identifier.issn00404020en_US
dc.identifier.other2-s2.0-84884670860en_US
dc.identifier.other10.1016/j.tet.2013.08.070en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84884670860&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/52194-
dc.description.abstractSix new β-carboline-type indole alkaloid glycosides, ophiorrhisides A-F (1-6), were isolated from Ophiorrhiza trichocarpon (Rubiaceae) collected in Thailand. Ophiorrhisides A (1) and B (2) possess a lactam function in the C ring and a unique biose residue in the molecule. Ophiorrhiside F (6) has a highly oxidized C ring with a 1,2-dicarbonyl function at C-5 and C-6 positions as well as a double bond between C-3 and C-14. © 2013 Elsevier Ltd. All rights reserved.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleβ-Carboline-type indole alkaloid glycosides from Ophiorrhiza trichocarponen_US
dc.typeJournalen_US
article.title.sourcetitleTetrahedronen_US
article.volume69en_US
article.stream.affiliationsChiba Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
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