Journal of Natural Products · 2015 · 53 citations · 21 references
Life SciencesBiochemistryPharmacologyCarbohydrate ChemistryPlant BiochemistryStructure-activity RelationshipsMedicinal PlantsMolecular SimilarityTannin AnalysisTannin ChemistryTannin PlantsAnti-inflammatory ActivityCondensed TanninsFree Radical GenerationFree Radical ScavengingHydrolyzable TanninsRadical ScavengersTannin CharacterizationTannin-based Natural Products
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).
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Antioxidant activity and mechanism of Rhizoma Cimicifugae
Xican Li, Jing Lin, Yaoxiang Gao et al. · Chemistry Central Journal · 2012 · 186 citations · Full text
New Methods of Analyzing Tannins
Takuo Okuda, Takashi Yoshida, Tsutomu Hatano · Journal of Natural Products · 1989 · 172 citations