dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorInst Bot
dc.contributorUniversidade de São Paulo (USP)
dc.date.accessioned2014-05-20T15:28:14Z
dc.date.accessioned2022-10-05T16:47:37Z
dc.date.available2014-05-20T15:28:14Z
dc.date.available2022-10-05T16:47:37Z
dc.date.created2014-05-20T15:28:14Z
dc.date.issued2003-09-01
dc.identifierPhytochemistry. Oxford: Pergamon-Elsevier B.V., v. 64, n. 2, p. 549-553, 2003.
dc.identifier0031-9422
dc.identifierhttp://hdl.handle.net/11449/38076
dc.identifier10.1016/S0031-9422(03)00153-5
dc.identifierWOS:000185421800023
dc.identifier2518006820764120
dc.identifier4702004904231248
dc.identifier1308042794786872
dc.identifier4484083685251673
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3909464
dc.description.abstractThree seco-iridoids 7-methoxydidcrrosidc, 6'-O-acetyldiderroside and 8-O-tigloyldiderroside, were isolated from the wood bark of Calycophyllum spruceanum together with the known iridoids loganetin, loganin and the seco-iridoids secoxyloganin, kingiside and diderroside. Their structures were elucidated by means of NMR and MS spectral data analysis. Using NOE correlations and coupling constants, the relative stereochernistry of the new derivatives was established. 7-Methoxydiderroside, 6'-O-acetyldiderroside and the known secoxyloganin and diderroside showed in vitro activity against trypomastigote forms of Trypanosonla Cruzi, with IC50 values of 59.0, 90.2, 74,2 and 84.9 mug/mL, respectively and were compared to the standard gentian violet (IC50 7.5 mug/ml). (C) 2003 Elsevier Ltd. All rights reserved.
dc.languageeng
dc.publisherElsevier B.V.
dc.relationPhytochemistry
dc.relation3.186
dc.relation1,048
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectCalycophyllum spruceanum
dc.subjectRubiaceae
dc.subjectiridoids
dc.subjectseco-iridoids
dc.subjectantitrypanosomal activity
dc.titleseco-Irldoids from Calycophyllum spruceanum (Rubiaceae)
dc.typeArtigo


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