| Literature DB >> 17063642 |
Birgit Benedek1, Bernard Weniger, Irene Parejo, Jaume Bastida, Gabriel Jaime Arango, Annelise Lobstein, Caries Codina.
Abstract
Two biflavones, ochnaflavone (1) and 2",3"-dihydroochnaflavone (2), and two isoflavones, 5,7,4'-trihydroxy-3',5'-dimethoxyisoflavone (piscigenin) (3) and 5,4'-dihydroxy-7,3',5'-trimethoxyisoflavone (4), a new natural compound, were isolated from the leaves of Godoya antioquiensis (Ochnaceae). Their structures were determined on the basis of spectral data and by comparison with data reported in the literature. The isolated compounds were evaluated for their radical scavenging activity using the NBT (nitrobluetetrazolium)/hypoxanthine superoxide and the .OH/luminol chemiluminescence methods. The isolated isoflavones were found to exhibit a strong hydroxyl radical scavenging activity and a moderate inhibition of the superoxide anion, whereas the two biflavones were inactive in the superoxide anion assay and showed a low hydroxyl radical scavenging activity.Entities:
Mesh:
Substances:
Year: 2006 PMID: 17063642 DOI: 10.1055/s-0031-1296768
Source DB: PubMed Journal: Arzneimittelforschung ISSN: 0004-4172