New antifungal terpenoid glycosides from Alibertia edulis (Rubiaceae). (Articolo in rivista)

Type
Label
  • New antifungal terpenoid glycosides from Alibertia edulis (Rubiaceae). (Articolo in rivista) (literal)
Anno
  • 2008-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1002/hlca.200890147 (literal)
Alternative label
  • Candida da Silva V; Soares Mendes Giannini MJ; Carbone V; Piacente S; Pizza C; da Silva Bolzani V; Nasser Lopes M.; (2008)
    New antifungal terpenoid glycosides from Alibertia edulis (Rubiaceae).
    in Helvetica chimica acta; Wiley-VCH Verlag Gmbh, Weinheim (Germania)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Candida da Silva V; Soares Mendes Giannini MJ; Carbone V; Piacente S; Pizza C; da Silva Bolzani V; Nasser Lopes M.; (literal)
Pagina inizio
  • 1355 (literal)
Pagina fine
  • 1362 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 91 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Chemistry Institute, Sa˜o Paulo State University, UNESP, C.P. 355, CEP 14801-970, Araraquara,Sa˜o Paulo, Brazil Faculty of Pharmaceutical Sciences, Sa˜o Paulo State University, UNESP, CEP 14801-902, Araraquara, Sa˜o Paulo, Brazil Proteomic and Biomolecular Mass Spectrometry Center, Institute of Food Science, CNR, Via Roma, 52 a/c, I-83100, Avellino Dipartimento di Scienze Farmaceutiche, Universita degli Studi di Salerno, via Ponte Don Melillo, I-84084 Fisciano (SA) (literal)
Titolo
  • New antifungal terpenoid glycosides from Alibertia edulis (Rubiaceae). (literal)
Abstract
  • Phytochemical investigation from the stems of Alibertia edulis led to the isolation and identification of a new iridoid 6b-hydroxy-7-epigardoside methyl ester (1) and a new saponin 3b-O-[a-l-rhamnopyranosyl-( 1!2)-O-b-d-glucopyranosyl-(1!2)-O-b-d-glucopyranosyl]-28-O-b-d-glucopyranoside pomolate (2), along with three known compounds, shanzhiside methyl ester (3), ixoside (4), and 3,4,5- trimethoxyphenyl 1-O-b-d-apiofuranosyl-(1!6)-O-b-d-glucopyranoside (5). The structures of 1 and 2 were established on the basis of their spectroscopic data. Iridoid 1 and saponin 2 exhibited moderate inhibitory activities against Candida albicans and C. krusei in a dilution assay. (literal)
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