A Dimeric Triterpenoid Glycoside and Flavonoid Glycosides with Free Radical-Scavenging Activity Isolated from Rubus rigidus var. camerunensis

被引:34
|
作者
Nguelefack, Telesphore Benoit [2 ]
Mbakam, Felicite Hermine Kamga [2 ]
Tapondjou, Leon Azefack [3 ]
Watcho, Pierre [2 ]
Nguelefack-Mbuyo, Elvine Pami [2 ]
Ponou, Beaudelaire Kemvoufo [3 ]
Kamanyi, Albert [2 ]
Park, Hee-Juhn [1 ]
机构
[1] Sangji Univ, Dept Pharmaceut Engn, Wonju 220702, South Korea
[2] Univ Dschang, Fac Sci, Lab Anim Physiol & Phytopharmacol, Dschang, Cameroon
[3] Univ Dschang, Fac Sci, Lab Environm & Appl Chem, Dschang, Cameroon
关键词
Rubus rigidus; Antioxidant; Flavonoids; Saponins; Structure-activity-relationship; ANTIOXIDANT ACTIVITY; LIPID-PEROXIDATION; LIVER-DAMAGE; SAPONINS; INHIBITORS; EXTRACTS; FRACTION; STRESS; ESTERS; LEAVES;
D O I
10.1007/s12272-011-0404-9
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The aerial part of Rub us rigidus var. camerunensis (Rosaceae) is used to treat respiratory and cardiovascular disorders in the Cameroonian traditional medicine. The ethanol extract exhibited more potent antioxidant activity (E(max)s of 119% and 229% activity on DPPH and beta-carotene test) than aqueous extract. Bioactivity-guided fractionation of the ethanol extract based on free radical-scavenging assay (DPPH assay) afforded five flavonoid glycosides (four flavonol glycosides and an anthocyanin) and three glucosides of 19 alpha-hydroxyursane-type triterpenoid (two monomeric and one dimeric triterpenoids). The flavonoids were identified as kaempferol 3-O-(2 ''-O-E-p-coumaroy1)-beta-D-glucopyranoside (1), kaempferol-3-O-beta-D-glucopyranoside (astragalin, 2), kaempferol-3-O-alpha-L-arabinofuranoside (juglanin, 3), quercetin-3-O-beta-D-glucopyranoside (isoquercitrin, 4), pelargonidin-3-O-beta-D-glucopyranoside (callistephin, 5). The three triterpenoids were 2 alpha, 3 beta, 19 alpha, 23-tetrahydroxyurs-12-ene-28-O-beta-D-glucopyranosyl ester (nigaichigoside F1, 6), 2 alpha, 3 beta, 19 alpha-trihydroxyurs-12-ene-23-carboxy1-28-O-beta-D-glucopyranosyl ester (suavissimoside R-1, 7) as monomeric triterpenoids and coreanoside F-1 (8) as a dimeric triterpenoid. The flavonoids exhibited potent antioxidant activities (66 to 93.56% against DPPH radical) and they were also active on beta-carotene test. Coreanoside F-1 exhibited a 63% antioxidant activity, meanwhile the other two triterpenoids showed a weak activity. Three important facts on structure-activity relationship were observed: Compound 8, a dimeric triterpenoid glycoside, strongly enhanced antioxidant activity of its monomers, compound 3 with 3-O-alpha-L-arabinofuranyl has much more potent activity than compound 2 with 3-O-beta-D-glucopyranosyl, and antocyanin (5) is more potent than its corresponding flavonol glycosides.
引用
收藏
页码:543 / 550
页数:8
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