Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/12066
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dc.contributor.authorRukachaisirikul T.
dc.contributor.authorKumjun S.
dc.contributor.authorSuebsakwong P.
dc.contributor.authorApiratikul N.
dc.contributor.authorSuksamrarn A.
dc.date.accessioned2021-04-05T03:01:46Z-
dc.date.available2021-04-05T03:01:46Z-
dc.date.issued2021
dc.identifier.issn14786419
dc.identifier.other2-s2.0-85098625668
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/12066-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85098625668&doi=10.1080%2f14786419.2019.1614576&partnerID=40&md5=cda503c2b4dc878d8cb61ef0e8c22aa1
dc.description.abstractPhytochemical investigation of the roots of Cissampelos pareira Linn. led to the isolation of one new pyrrole alkaloid, cissampeline (1), together with ten known alkaloids, (−)-curine (2), (−)-cyclanoline (3), (+)-tetrandrine (4), (+)-obaberine (5), (+)-obamegine (6), (−)-oblongine (7), (+)-homoaromoline (8), (−)-nor-N׳-chondrocurine (9), trans-N-feruloyltyramine (10) and (+)-coclaurine (11). Their structures were elucidated by extensive NMR and MS spectroscopic analyses. Interestingly, compound 1 represents the first example of pyrrole alkaloid found in the genus Cissampelos. Moreover, compounds 5-11 were isolated for the first time from this genus. Among them, compound 6 showed the highest anti-acetylcholinesterase activity with an IC50 value of 3.26 µM, whereas compound 8 displayed the most potent cytotoxicity against human colon cancer (HT29) cells with an IC50 value of 7.89 µM. © 2019 Informa UK Limited, trading as Taylor & Francis Group.
dc.rightsSrinakharinwirot University
dc.titleA new pyrrole alkaloid from the roots of Cissampelos pareira
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationNatural Product Research. Vol 35, No.1 (2021), p.80-87
dc.identifier.doi10.1080/14786419.2019.1614576
Appears in Collections:Scopus 1983-2021

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