| Literature DB >> 25918997 |
Jia-Bao Liu1, Ya-Si Ding1, Ying Zhang1, Jia-Bao Chen1, Bao-Song Cui1, Jin-Ye Bai1, Ming-Bao Lin1, Qi Hou1, Pei-Cheng Zhang1, Shuai Li1.
Abstract
Twelve hydrolyzable tannins were obtained from the twigs of Myricaria bracteata, including two new hellinoyl-type dimers, bracteatinins D1 (1) and D2 (2); a new hellinoyl-type trimer, bracteatinin T1 (3); two known monomers, nilotinin M4 (4) and 1,3-di-O-galloyl-4,6-O-(aS)-hexahydroxydiphenoyl-β-d-glucose (5); six known dimers, tamarixinin A (6), nilotinin D8 (7), hirtellins A (10), B (9), and E (8), and isohirtellin C (11); and a known trimer, hirtellin T3 (12). The structures of the tannins were elucidated by spectroscopic data analysis and comparisons to known tannins. All compounds were evaluated as free radical scavengers using 1,1-diphenyl-2-picrylhydrazyl and hydroxy radicals and compared to the activity of BHT and Trolox. Compound 6 showed a significant anti-inflammatory effect on croton oil-induced ear edema in mice (200 mg/kg, inhibition rate 69.8%) and on collagen-induced arthritis in DBA/1 mice (20 mg/kg, inhibition rate 46.0% at day 57).Entities:
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Year: 2015 PMID: 25918997 DOI: 10.1021/np500953e
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050