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dc.contributor.authorWantida Chaiyanaen_US
dc.contributor.authorJan Schripsemaen_US
dc.contributor.authorKornkanok Ingkaninanen_US
dc.contributor.authorSiriporn Okonogien_US
dc.date.accessioned2018-09-04T09:22:45Z-
dc.date.available2018-09-04T09:22:45Z-
dc.date.issued2013-04-15en_US
dc.identifier.issn1618095Xen_US
dc.identifier.issn09447113en_US
dc.identifier.other2-s2.0-84875950130en_US
dc.identifier.other10.1016/j.phymed.2012.12.016en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84875950130&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/52256-
dc.description.abstractGuided by the acetylcholinesterase inhibiting activity, the bisindole alkaloid 3′-R/S-hydroxyvoacamine was isolated from a stem extract of Tabernaemontana divaricata, a plant used in Thailand in traditional rejuvenation remedies for improving the memory. The structure of the alkaloid was elucidated by extensive use of NMR spectroscopy and the complete assignment of the1H and13C NMR spectra is reported. The alkaloid acted as a non-competitive inhibitor against AChE with an IC50value of 7.00 ± 1.99 μM. An HPLC method was developed for the quantitative analysis of the AChE inhibitor. It suggested that there was 12.4% (w/w) of 3′-R/S-hydroxyvoacamine in the alkaloid enriched fraction of T. divaricata stem. © 2013 Elsevier GmbH. All rights reserved.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.title3′-R/S-Hydroxyvoacamine, a potent acetylcholinesterase inhibitor from Tabernaemontana divaricataen_US
dc.typeJournalen_US
article.title.sourcetitlePhytomedicineen_US
article.volume20en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsUniversidade Estadual do Norte Fluminenseen_US
article.stream.affiliationsNaresuan Universityen_US
Appears in Collections:CMUL: Journal Articles

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