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Nat Prod Res ; 35(12): 2082-2085, 2021 Jun.
Article in English | MEDLINE | ID: mdl-31402707

ABSTRACT

A phytochemical investigation of Physalis minima led to the isolation of six withanolides, including withanolide E (1), withaperuvin C (2), 4ß-hydroxywithanolide E (3), 28-hydroxywithaperuvin C (4), physaperuvin G (5), and 4-deoxywithaperuvin (6). Their chemical structures were elucidated by 1 D-NMR and 2 D-NMR data, as well as comparison with the data reported in the literature. All isolated compounds were evaluated for their cytotoxic activity against HepG2, SK-LU-1, and MCF7 cancer cell lines. As the obtained results, compounds 1 and 3 displayed the strongest cytotoxicity against HepG2, SK-LU-1, and MCF7 cell lines with IC50 value ranging from 0.051 ± 0.004 to 0.86 ± 0.09 µg/mL.


Subject(s)
Antineoplastic Agents, Phytogenic/chemistry , Antineoplastic Agents, Phytogenic/pharmacology , Physalis/chemistry , Withanolides/chemistry , Cell Line, Tumor , Drug Screening Assays, Antitumor , Hep G2 Cells , Humans , MCF-7 Cells , Magnetic Resonance Spectroscopy , Molecular Structure , Plant Components, Aerial/chemistry , Plant Extracts/chemistry , Structure-Activity Relationship , Withanolides/pharmacology
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