Cytotoxic Isopimarane Diterpenoids from Kaempferia koratensis Rhizomes

dc.contributor.authorKongwaen P.
dc.contributor.authorBoonsombat J.
dc.contributor.authorThongnest S.
dc.contributor.authorRuchisansakun S.
dc.contributor.authorMahidol C.
dc.contributor.authorRuchirawat S.
dc.contributor.otherMahidol University
dc.date.accessioned2023-05-25T17:22:16Z
dc.date.available2023-05-25T17:22:16Z
dc.date.issued2023-04-01
dc.description.abstractTwo new isopimarane diterpenoids, koratanes A and B, were identified from the rhizomes of Kaempferia koratensis Picheans., Zingiberaceae, together with thirteen known isopimarane diterpenoids. Spectroscopic evidence was used to determine the structures. CD spectra were applied to determine the absolute configuration of koratanes A. The isolated compounds were evaluated for their cytotoxicity against human HL-60 and MOLT-3 leukemia cells, T-47D breast cancer cells, and MRC-5 healthy cells. Among the isolates, compounds named koratanes A, koratanes B, boesenberrol J, saraburane B, kaempulchraol A, kaempulchraol B, kaempulchraol C, and curcumrinol A showed IC50 values ranging from 42.10 to 56.57 μM against MOLT-3 cancer cell line. Koratanes B and galangol D were the most active against HL-60 and T-47D with IC50 values of 55.62 and 79.51 μM, respectively. Graphical Abstract: [Figure not available: see fulltext.].
dc.identifier.citationRevista Brasileira de Farmacognosia Vol.33 No.2 (2023) , 415-421
dc.identifier.doi10.1007/s43450-023-00359-w
dc.identifier.eissn1981528X
dc.identifier.scopus2-s2.0-85147287988
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/82846
dc.rights.holderSCOPUS
dc.subjectPharmacology, Toxicology and Pharmaceutics
dc.titleCytotoxic Isopimarane Diterpenoids from Kaempferia koratensis Rhizomes
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85147287988&origin=inward
oaire.citation.endPage421
oaire.citation.issue2
oaire.citation.startPage415
oaire.citation.titleRevista Brasileira de Farmacognosia
oaire.citation.volume33
oairecerif.author.affiliationLaboratory of Medicinal Chemistry
oairecerif.author.affiliationLaboratory of Natural Products
oairecerif.author.affiliationChulabhorn Royal Academy
oairecerif.author.affiliationMahidol University
oairecerif.author.affiliationMinistry of Higher Education, Science, Research and Innovation

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