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Identification of flavonoids and flavonoid rhamnosides from Rhododendron mucronulatum for. albiflorum and their inhibitory activities against aldose reductase

机译:鉴定自杜鹃杜鹃中的黄酮类和黄酮类鼠李糖苷。白花及其对醛糖还原酶的抑制活性

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To investigate the therapeutic potential of compounds from natural sources, Rhododendron mucronulatum for. albiflorum flowers (RMAF) and R. mucronulatum flowers (RMF) were tested for inhibition of aldose reductase (AR). The methanol extracts of RMAF and RMF exhibited AR inhibitory activities (IC_(50) values 1.07 and 1.29 μg/mL, respectively). The stepwise polarity fractions of RMAF were tested for in vitro inhibition of AR from rat lenses. Of these, the ethyl acetate (EtOAc) fraction exhibited AR inhibitory activity (IC_(50)0.15 μg/mL). A chromatography of the active EtOAc fraction of RMAF led to the isolation of six flavonoids, which were identified by spectroscopic analysis as kaempferol (1), afzelin (2), quercetin (3), querci-trin (4), myricetin (5) and myricitrin (6). Compounds 1-6 exhibited high AR inhibitory activity, with IC_(50) values of 0.79, 0.31, 0.48, 0.13, 11.92 and 2.67 μg/mL, respectively. HPLC/UV analysis revealed that the major flavonoids of RMAF and RMF are quercitrin (4) and myricitrin (6). Our results suggest that RMAF containing these six flavonoids could be a useful natural source in the development of a novel AR inhibitory agent against diabetic complications.
机译:为了研究天然来源化合物的治疗潜力,杜鹃花为。测试了白花花(RMAF)和粘液杜鹃花(RMF)对醛糖还原酶(AR)的抑制作用。 RMAF和RMF的甲醇提取物表现出AR抑制活性(IC_(50)值分别为1.07和1.29μg/ mL)。测试了RMAF的逐步极性级分对大鼠晶状体AR的体外抑制作用。其中,乙酸乙酯(EtOAc)级分显示出AR抑制活性(IC_(50)0.15μg/ mL)。对RMAF的活性EtOAc馏分进行色谱分析,分离出6个类黄酮,通过光谱分析将其鉴定为山fer酚(1),黄素(2),槲皮素(3),槲皮素(4),杨梅素(5)和杨梅素(6)。化合物1-6表现出较高的AR抑制活性,IC_(50)值分别为0.79、0.31、0.48、0.13、11.92和2.67μg/ mL。 HPLC / UV分析表明,RMAF和RMF的主要类黄酮为槲皮苷(4)和杨梅苷(6)。我们的结果表明,包含这六个类黄酮的RMAF可能是开发抗糖尿病并发症的新型AR抑制剂的有用天然来源。

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