Fungitoxic non-glycosidic iridoids from Alibertia macrophylla

dc.contributorUniversidade Estadual Paulista (UNESP)
dc.creatorYoung, M.Claudia M.
dc.creatorBraga, Marcia R.
dc.creatorDietrich, Sonia M.C.
dc.creatorGottlieb, Hugo E.
dc.creatorTrevisan, Ligia M.V.
dc.creatorBolzani, Vanderlan da Silva
dc.date2014-05-27T11:17:29Z
dc.date2016-10-25T21:25:35Z
dc.date2014-05-27T11:17:29Z
dc.date2016-10-25T21:25:35Z
dc.date1992-10-01
dc.date.accessioned2017-04-06T09:38:21Z
dc.date.available2017-04-06T09:38:21Z
dc.identifierPhytochemistry, v. 31, n. 10, p. 3433-3435, 1992.
dc.identifier0031-9422
dc.identifierhttp://hdl.handle.net/11449/132333
dc.identifierhttp://acervodigital.unesp.br/handle/11449/132333
dc.identifier10.1016/0031-9422(92)83701-Y
dc.identifierWOS:A1992JT41000025
dc.identifier2-s2.0-3042962493
dc.identifierhttp://dx.doi.org/10.1016/0031-9422(92)83701-Y
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/942874
dc.descriptionThe aqueous alcohol extract of the leaves of Alibertia macrophylla afforded two epimeric pairs of iridoid aglycones and one of them showed high inhibitory activity against Aspergillus niger, Cladosporium sphaerospermum, C. cladosporioides and Colletotrichum gloesporioides. Three of the compounds are reported for the first time from natural sources. Their structures were established on the basis of spectroscopic studies, mainly through 13C NMR analysis. © 1992.
dc.languageeng
dc.relationPhytochemistry
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectAlibertia macrophylla
dc.subjectantifungal activity.
dc.subjectnon-glycosidic iridoids
dc.subjectRubiaceae
dc.titleFungitoxic non-glycosidic iridoids from Alibertia macrophylla
dc.typeOtro


Este ítem pertenece a la siguiente institución