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Nat Prod Res ; 36(7): 1774-1780, 2022 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-32901507

RESUMEN

Phytochemical investigation of the leaves of Lepisanthes rubiginosa led to the isolation of two new glycosides, lepisantheside A (1) and lepisantheside B (2), together with two known compounds acutoside A (3) and 3-O-[ß-D-xylopyranosyl-(1→3)-ß-D-glucopyranosyl-]-oleanolic acid (4). Their structures were elucidated by means of spectroscopic methods (HR-ESI-MS, 1D and 2D NMR), and by comparison with the reported data. The cytotoxicity of compounds 1-4 against four human cancer cell lines (KB, HepG2, SK-LU-1 and MCF7) was evaluated. Compound 4 exhibited significant activity with IC50 values of 9.57, 6.66, 6.97 and 18.32 µM, respectively, in comparison with the postive control ellipticine.


Asunto(s)
Ácido Oleanólico , Triterpenos , Glicósidos/química , Humanos , Estructura Molecular , Ácido Oleanólico/análogos & derivados , Ácido Oleanólico/química , Hojas de la Planta/química , Triterpenos/química , Vietnam
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