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Mar Drugs ; 22(2)2024 Jan 24.
Artículo en Inglés | MEDLINE | ID: mdl-38393029

RESUMEN

Five new diisoprenyl cyclohexene-type meroterpenoids, aspergienynes J-N (1-5), along with three known analogues (6-8), were obtained from the mangrove endophytic fungal strain Aspergillus sp. GXNU-Y85. The chemical structures, including their absolute configurations, were established via spectroscopic data and comparison of experimental and calculated ECD spectra. Cytotoxicity assay results indicated that compound 8 had strong cytotoxicity against HeLa cancer cells, and its IC50 value was 11.8 µM. In addition, flow cytometry analysis revealed that the cytotoxicity of 8 was due to the induction of G1 cell cycle arrest and apoptosis in HeLa cells.


Asunto(s)
Antineoplásicos , Aspergillus , Humanos , Estructura Molecular , Células HeLa , Aspergillus/química , Análisis Espectral , Antineoplásicos/farmacología , Antineoplásicos/metabolismo
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