New antifungal terpenoid glycosides from Alibertia edulis (Rubiaceae)
Contribuinte(s) |
Universidade Estadual Paulista (UNESP) |
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Data(s) |
20/05/2014
20/05/2014
01/01/2008
|
Resumo |
Phytochemical investigation from the stems of Alibertia edulis led to the isolation and identification of a new iridoid 6 beta-hydroxy-7-epigardoside methyl ester (1) and a new saponin 3 beta-O-[alpha-L-rhamnopyranosyl-(1 -> 2)-O-beta-D-glucopyranosyl-(1 -> 2)-O-beta-D-glucopyranosyl]-28-O-beta-D-glucopyranoside pomolate (2), along with three known compounds, shanzhiside methyl ester (3), ixoside (4), and 3,4,5-trimethoxyphenyl 1-O-beta-D-apiofuranosyl-(1 -> 6)-O-beta-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. |
Formato |
1355-1362 |
Identificador |
http://dx.doi.org/10.1002/hlca.200890147 Helvetica Chimica Acta. Malden: Wiley-blackwell, v. 91, n. 7, p. 1355-1362, 2008. 0018-019X http://hdl.handle.net/11449/26031 10.1002/hlca.200890147 10.1002/hlca.200890147 WOS:000258088800017 |
Idioma(s) |
eng |
Publicador |
Wiley-Blackwell |
Relação |
Helvetica Chimica Acta |
Direitos |
closedAccess |
Tipo |
info:eu-repo/semantics/article |