| Literature DB >> 16076635 |
Kênnia R Rezende1, Solange C Davino, Sílvia B M Barros, Massuo J Kato.
Abstract
Aryltetralone lignans bearing methylenedioxy groups (1a-b; 2a-b) were isolated from seeds of Virola sebifera. Their antioxidant activities were evaluated by inhibition of lipid peroxidation as indicated by TBARS and chemiluminescence emission (CL) assays. The lignan 1c, 'having a 2'-hydroxy-4',5'-methylenedioxyphenyl group, was the most active compound with TBARS/CL Q 1/2 values of 0.89 and 0.10 microg/mL, respectively. The catechol derivatives 3 and 4, obtained by demethylenation of lignans 1a and 2a, were of similar activity to 1c, and all were much more effective as antioxidants than alpha-tocopherol.Entities:
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Year: 2005 PMID: 16076635 DOI: 10.1080/14786410412331302118
Source DB: PubMed Journal: Nat Prod Res ISSN: 1478-6419 Impact factor: 2.861