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dc.contributor.authorFuentes-Ríos, David
dc.contributor.authorOrtigosa Palomo, Alba
dc.contributor.authorQuiñonero Muñoz, Francisco José 
dc.contributor.authorMelguizo Alonso, Consolación 
dc.contributor.authorOrtiz Quesada, Raúl 
dc.contributor.authorPrados Salazar, José Carlos 
dc.contributor.authorDíaz, Amelia
dc.contributor.authorLópez Romero, Juan Manuel
dc.date.accessioned2024-05-10T10:45:50Z
dc.date.available2024-05-10T10:45:50Z
dc.date.issued2024-03-20
dc.identifier.citationACS Omega 2024, 9, 13, 15718–15722 [https://doi.org/10.1021/acsomega.4c01914]es_ES
dc.identifier.urihttps://hdl.handle.net/10481/91644
dc.descriptionThe Supporting Information is available free of charge at https://pubs.acs.org/doi/10.1021/acsomega.4c01914.es_ES
dc.description.abstractA 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.es_ES
dc.description.sponsorshipJunta de Andalucía funding, projects FQM397 and UMA20 FEDERJA84es_ES
dc.language.isoenges_ES
dc.publisherAmerican Chemical Societyes_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleIsolation and Antitumoral Effect of a New Siphonochilone Derivative from African Gingeres_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1021/acsomega.4c01914
dc.type.hasVersionVoRes_ES


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
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