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A new languidulane diterpenoid from Salvia mexicana var. Mexicana
dc.creator | Frontana-Uribe, Bernardo Antonio | |
dc.creator | Escárcega-Bobadilla, Martha Verónica | |
dc.creator | Estrada-Reyes, Rosa | |
dc.creator | Morales-Serna, José Antonio | |
dc.creator | Salmón, Manuel | |
dc.creator | Cárdenas, Jorge | |
dc.date.accessioned | 2017-06-30T01:41:10Z | |
dc.date.available | 2017-06-30T01:41:10Z | |
dc.date.issued | 2011 | es_ES |
dc.identifier | 1519 | es_ES |
dc.identifier.uri | http://www.mdpi.com/1420-3049/16/10/8866 | es_ES |
dc.identifier.uri | http://repositorio.inprf.gob.mx/handle/123456789/6198 | |
dc.identifier.uri | https://doi.org/10.3390/molecules16108866 | es_ES |
dc.language.iso | eng | es_ES |
dc.relation | 16 (10) 8866-8873 p. | es_ES |
dc.relation | versión del editor | es_ES |
dc.rights | acceso cerrado | es_ES |
dc.title | A new languidulane diterpenoid from Salvia mexicana var. Mexicana | es_ES |
dc.type | article | es_ES |
dc.contributor.affiliation | Instituto de Química, Universidad Nacional Autónoma de México, Circuito Exterior, Ciudad Universitaria, 04510 México D.F., México. | es_ES |
dc.contributor.email | rjcp@unam.mx | es_ES |
dc.relation.jnabreviado | MOLECULES | es_ES |
dc.relation.journal | Molecules : a Journal of Synthetic Chemistry and Natural Product Chemistry | es_ES |
dc.identifier.place | Suiza | es_ES |
dc.date.published | 2011 | es_ES |
dc.identifier.organizacion | Instituto Nacional de Psiquiatría Ramón de la Fuente Muñiz | es_ES |
dc.identifier.eissn | 1420-3049 | es_ES |
dc.identifier.doi | 10.3390/molecules16108866 | es_ES |
dc.description.month | Oct | es_ES |
dc.description.abstractotrodioma | From the aerial parts of Salvia mexicana var. mexicana, two C-10 epimers (_ and _) of salvimexicanolide were isolated. Our interpretation of the data, especially the 13C NMR, led us to conclude that the previously described 13C-NMR spectrum of the _-epimer was not accurately assigned and it actually corresponds to the _-epimer. The structures proposed for the salvimexicanolides were verified by means of NOESY experiments. Dugesin B, arbutin, naringenin and the mixture of oleanolic and ursolic acids were also isolated from this Salvia spp | es_ES |
dc.subject.ko | Arbutin | es_ES |
dc.subject.ko | isolation & purification | es_ES |
dc.subject.ko | Diterpenes | es_ES |
dc.subject.ko | chemistry | es_ES |
dc.subject.ko | Diterpenes | es_ES |
dc.subject.ko | isolation & purification | es_ES |
dc.subject.ko | Flavanones | es_ES |
dc.subject.ko | isolation & purification | es_ES |
dc.subject.ko | Lamiaceae | es_ES |
dc.subject.ko | Magnetic Resonance Spectroscopy | es_ES |
dc.subject.ko | Oleanolic Acid | es_ES |
dc.subject.ko | isolation & purification | es_ES |
dc.subject.ko | Plant Components, Aerial | es_ES |
dc.subject.ko | Plant Extracts | es_ES |
dc.subject.ko | chemistry | es_ES |
dc.subject.ko | Salvia | es_ES |
dc.subject.ko | chemistry | es_ES |
dc.subject.ko | Triterpenes | es_ES |
dc.subject.ko | isolation & purification | es_ES |
dc.subject.ko | Diterpenes | es_ES |
dc.subject.ko | Flavanones | es_ES |
dc.subject.ko | Plant Extracts | es_ES |
dc.subject.ko | Triterpenes | es_ES |
dc.subject.ko | Arbutin | es_ES |
dc.subject.ko | Oleanolic Acid | es_ES |
dc.subject.ko | naringenin | es_ES |
dc.subject.ko | ursolic acid | es_ES |
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