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dc.rights.licensehttp://creativecommons.org/licenses/by-nc-nd/4.0es_MX
dc.creatorOrtega, Alfredo-
dc.date.accessioned2020-02-11T21:20:43Z-
dc.date.available2020-02-11T21:20:43Z-
dc.date.issued2020-
dc.identifier.urihttp://rdu.iquimica.unam.mx/handle/20.500.12214/1203-
dc.description.abstractPhytochemical investigation of the leaves andflowers fromSalvia hirsutaled to the isolation of thefivemicrophyllane-type diterpenoids (1e5), and twoflavones (6e7). Hirsutolides constituted new diterpe-noids containing a 5-hydroxyfuran-2(5H)-one and were isolated as an epimeric mixture at C-3 and C-15.The structures of the isolated compounds were established through the analysis of their NMR spectro-scopic and MS spectrometric data; and confirmed by single-crystal X-ray diffraction studies. Cytotoxicand MDR modulatory activities of compounds1-5 were determined.es_MX
dc.language.isoenges_MX
dc.relation.urihttp://www.elsevier.com/locate/molstruces_MX
dc.rightsinfo:eu-repo/semantics/closedAccesses_MX
dc.sourceJournal of Molecular Structure (ISSN 0022-2860) 1203, 127409es_MX
dc.titleNMR and SC-XRD analyses of a solid solution of diastereomers of microphyllane diterpenoids from Salvia hirsutaes_MX
dc.typeinfo:eu-repo/semantics/articlees_MX
dc.creator.idinfo:eu-repo/dai/mx/orcid/0000-0002-1746-0981es_MX
dc.subject.ctiinfo:eu-repo/classification/cti/2es_MX
dc.subject.keywordsSalvia hirsutaes_MX
dc.subject.keywordsMultidrug-resistancees_MX
dc.subject.keywordsMycrophyllane diterpenoidses_MX
dc.subject.keywordsModulatorses_MX
dc.type.urihttps://doi.org/10.1016/j.molstruc.2019.127409es_MX
dc.creator.twoCárdenas, Jorge-
dc.creator.threeToscano, Rubén A.-
dc.creator.idtwoinfo:eu-repo/dai/mx/orcid/0000-0002-4096-2293es_MX
dc.creator.idthreeinfo:eu-repo/dai/mx/orcid/0000-0002-4380-9251es_MX
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