Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/12066
Title: A new pyrrole alkaloid from the roots of Cissampelos pareira
Authors: Rukachaisirikul T.
Kumjun S.
Suebsakwong P.
Apiratikul N.
Suksamrarn A.
Issue Date: 2021
Abstract: Phytochemical 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.
URI: https://ir.swu.ac.th/jspui/handle/123456789/12066
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85098625668&doi=10.1080%2f14786419.2019.1614576&partnerID=40&md5=cda503c2b4dc878d8cb61ef0e8c22aa1
ISSN: 14786419
Appears in Collections:Scopus 1983-2021

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