Publication:
A new alkaloid and a new benzaldehyde derivative from the twig of Zanthoxylum rhetsa (Roxb.) DC.

dc.contributor.authorLookpan T.
dc.contributor.authorVoravuthikunchai S.P.
dc.contributor.authorSitthisuk P.
dc.contributor.authorPoorahong W.
dc.contributor.authorWatanapokasin R.
dc.contributor.authorChakthong S.
dc.date.accessioned2022-12-14T03:16:53Z
dc.date.available2022-12-14T03:16:53Z
dc.date.issued2022
dc.date.issuedBE2565
dc.description.abstractA new alkaloid, 2-acetyl-4-methoxyfuro[2,3-b]quinoline (1), and a new benzaldehyde derivative, (2′S)-4-(2′-hydroxy-3′-methyl-3′-butenoxy)benzaldehyde (2), were isolated from the twig of Zanthoxylum rhetsa (Roxb.) DC. along with twenty-six known compounds (3−28). Their structures were determined by spectroscopic analysis (1D and 2D NMR spectroscopy and HRMS analysis) and comparison with data reported in the literature. Thirteen of the known compounds were evaluated for their cytotoxic activities against human cancer cell lines that included MDA-MB-231, SW1353, A549, and HCT116. (±)-8-Acetonyldihydronitidine (15) showed moderate cytotoxicity toward the SW1353 cancer cell line with an IC50 value of 18.90±0.39 µg/mL, and exhibited weak cytotoxic activity against MDA-MB-231, A549 and HCT116 cell lines with IC50 values of 49.86−71.32 µg/mL. © 2022 Informa UK Limited, trading as Taylor & Francis Group.
dc.format.mimetypeapplication/pdf
dc.identifier.citationFrontiers of Nursing. Vol 9, No.2 (2022), p.215-223
dc.identifier.doi10.1080/14786419.2022.2127708
dc.identifier.issn14786419
dc.identifier.urihttps://hdl.handle.net/20.500.14740/9101
dc.language.isoeng
dc.publisherTaylor and Francis Ltd.
dc.rights.holderScopus
dc.subject.otherAlkaloid
dc.subject.otherBenzaldehyde derivative
dc.subject.otherCytotoxicity
dc.subject.otherZanthoxylum rhetsa
dc.titleA new alkaloid and a new benzaldehyde derivative from the twig of Zanthoxylum rhetsa (Roxb.) DC.
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85139122793&doi=10.1080%2f14786419.2022.2127708&partnerID=40&md5=42ce08ae4dcaa300dc251c9b0551759e

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