Isolation and Antitumoral Effect of a New Siphonochilone Derivative from African Ginger
Metadatos
Mostrar el registro completo del ítemAutor
Fuentes-Ríos, David; Ortigosa Palomo, Alba; Quiñonero Muñoz, Francisco José; Melguizo Alonso, Consolación; Ortiz Quesada, Raúl; Prados Salazar, José Carlos; Díaz, Amelia; López Romero, Juan ManuelEditorial
American Chemical Society
Fecha
2024-03-20Referencia bibliográfica
ACS Omega 2024, 9, 13, 15718–15722 [https://doi.org/10.1021/acsomega.4c01914]
Patrocinador
Junta de Andalucía funding, projects FQM397 and UMA20 FEDERJA84Resumen
A new eusdesmane sesquiterpenoid, characterized as 3,5,8a-trimethyl-8-oxo-4,4a,5,6,7,8,8a,9-octahydronaphtho[2,3-b]furan-5-yl acetate (1), has been isolated from the rhizomes of the South African variety of wild ginger (Siphonochilus aethiopicus (Schweinf) B. L. Burtt). The compound was obtained by silica gel column chromatography. Its structure was elucidated by nuclear magnetic resonance spectroscopy (NMR) and mass-spectrometric (MS) analyses, including 1D-, 2D-NMR, and HR-LCMS. We also investigated the cytotoxic effect of 1 on a panel of cancer cell lines, human breast, pancreas, lung, colon, and central nervous system cancer lines. The data are not encouraging since its antitumor effect is poor. Nonetheless, the discovery of new molecules may provide a source of new compounds with important biological effects applicable to the field of medicine.