New ring-A modified cycloartane triterpenoids from Dysoxylum malabaricum bark: Isolation, structure elucidation and their cytotoxicity

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dc.contributor.authorBhardwaj N.
dc.contributor.authorGupta P.
dc.contributor.authorTripathi N.
dc.contributor.authorChakrabarty S.
dc.contributor.authorVerma A.
dc.contributor.authorKumari S.
dc.contributor.authorGautam V.
dc.contributor.authorRavikanth G.
dc.contributor.authorJain S.K.
dc.date.accessioned2025-01-13T07:05:45Z
dc.date.available2025-01-13T07:05:45Z
dc.date.issued2024
dc.description.abstractThe Genus Dysoxylum (Meliaceae) consists of approximately 80 species that are abundant in structurally diverse triterpenoids. The present study focused on isolating new triterpenoids from the bark of Dysoxylum malabaricum, one of the predominant species of Dysoxylum present in India. The methanol-dichloromethane bark extract was subjected to LCMS profiling followed by silica gel column chromatography and HPLC analysis to target new compounds. Two new ring A-modified cycloartane-type triterpenoids (1 and 2) were isolated from the bark extract. Spectroscopic methods like NMR, HRESIMS data, and electronic circular dichroism calculations elucidated the structures and absolute configurations of the isolated compounds. These compounds were evaluated for their cytotoxic potential against breast cancer cells and displayed notable cytotoxicity. Compound 1 exhibited the highest cytotoxicity against the MDA-MB-231 cells and induced apoptotic cell death. Also, it was able to inhibit glucose uptake and increase nitric oxide production in breast cancer cells. � 2024 Elsevier Inc.
dc.identifier.doi10.1016/j.steroids.2024.109390
dc.identifier.issn0039128X
dc.identifier.urihttps://dl.bhu.ac.in/ir/handle/123456789/2039
dc.language.isoen
dc.publisherElsevier Inc.
dc.subjectCycloartane
dc.subjectCytotoxicity
dc.subjectHPLC
dc.subjectLCMS
dc.subjectTriterpenoids
dc.titleNew ring-A modified cycloartane triterpenoids from Dysoxylum malabaricum bark: Isolation, structure elucidation and their cytotoxicity
dc.typeArticle
journal.titleSteroids
journalvolume.identifier.volume205

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