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DC Field | Value | Language |
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dc.contributor.author | Rukachaisirikul T. | |
dc.contributor.author | Kumjun S. | |
dc.contributor.author | Suebsakwong P. | |
dc.contributor.author | Apiratikul N. | |
dc.contributor.author | Suksamrarn A. | |
dc.date.accessioned | 2021-04-05T03:01:46Z | - |
dc.date.available | 2021-04-05T03:01:46Z | - |
dc.date.issued | 2021 | |
dc.identifier.issn | 14786419 | |
dc.identifier.other | 2-s2.0-85098625668 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/12066 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85098625668&doi=10.1080%2f14786419.2019.1614576&partnerID=40&md5=cda503c2b4dc878d8cb61ef0e8c22aa1 | |
dc.description.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. | |
dc.rights | Srinakharinwirot University | |
dc.title | A new pyrrole alkaloid from the roots of Cissampelos pareira | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Natural Product Research. Vol 35, No.1 (2021), p.80-87 | |
dc.identifier.doi | 10.1080/14786419.2019.1614576 | |
Appears in Collections: | Scopus 1983-2021 |
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