Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/56730
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dc.contributor.authorTadayoshi Onozawaen_US
dc.contributor.authorMariko Kitajimaen_US
dc.contributor.authorNoriyuki Kogureen_US
dc.contributor.authorNichakan Peerakamen_US
dc.contributor.authorDammrong Santiarwornen_US
dc.contributor.authorHiromitsu Takayamaen_US
dc.date.accessioned2018-09-05T03:29:31Z-
dc.date.available2018-09-05T03:29:31Z-
dc.date.issued2017-07-28en_US
dc.identifier.issn15206025en_US
dc.identifier.issn01633864en_US
dc.identifier.other2-s2.0-85026509664en_US
dc.identifier.other10.1021/acs.jnatprod.7b00290en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85026509664&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/56730-
dc.description.abstract© 2017 The American Chemical Society and American Society of Pharmacognosy. A new cyclopeptide, ophiorrhisine A (1), a new tetrahydroisoquinoline alkaloid, 7′,10-dide-O-methylcephaeline (2), two known β-carboline alkaloids, and four known tetrahydroisoquinoline alkaloids were isolated from Ophiorrhiza nutans (Rubiaceae). Compound 1 is a tetrapeptide possessing a 14-membered paracyclophane ring and a novel N,N,N-trimethyltyrosine residue in the side chain. The stereochemistry at the aryl-alkyl ether bond was different from that of other known 14-membered paracyclophanes. The structure of 2 was established by spectroscopic analysis and semisynthesis.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectMedicineen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleA Cyclopeptide and a Tetrahydroisoquinoline Alkaloid from Ophiorrhiza nutansen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Natural Productsen_US
article.volume80en_US
article.stream.affiliationsChiba Universityen_US
article.stream.affiliationsBurapha Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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