首页> 外文期刊>Journal of enzyme inhibition and medicinal chemistry. >Isolation of a new bioactive cinnamic acid derivative from the whole plant of Viola betonicifolia
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Isolation of a new bioactive cinnamic acid derivative from the whole plant of Viola betonicifolia

机译:从中提琴甲醛全植物中分离新的生物活性肉桂酸衍生物

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A new cinnamic acid derivative was isolated from the whole plant of Viola betonicifolia as off white needle. On the basis of various modern spectroscopic techniques including HREI-MS and 1D and 2D NMR, its structure was elucidated as 2,4-dihydroxy, 5-methoxy-cinnamic acid. It showed marked inhibition against DPPH (diphenyl-2-picryl hydrazyl) free radicals with IC50 = 124(+-)5.76 uM. The antioxidant property of the compound was compared with a-tocopherole and vitamin C having IC50 values 96(+-)0.46 and 90(+-)0.56 uM, respectively. In case of antiglycation assay, the compound exhibited moderate activity (IC50 = 355 (+-)7.56 uM) similar to standard compound, rutin (IC50 = 294(+-)0.56 uM). However, it was non-toxic to PC-3 cell line. It is concluded that 2,4-dihydroxy, 5-methoxy-cinnamic acid has antiglycation potential which was further augmented by its antioxidant activity and thus offered an ideal natural therapeutic option for the effective management of diabetes.
机译:从预甲醛的整个植物中分离出一种新的肉桂酸衍生物,如白色针。 基于各种现代光谱技术,包括HREI-MS和1D和2D NMR,其结构阐明为2,4-二羟基,5-甲氧基 - 肉桂酸。 它表现出对DPPH(二苯基-2- Picryl肼)自由基的显着抑制用IC50 = 124(+ - )5.76μm。 将化合物的抗氧化性与具有IC 50值96(+ - )0.46和90(+ - )0.56μm的α-生育液和维生素C进行比较。 在抗粘附测定的情况下,该化合物具有与标准化合物相似的中等活性(IC50 = 355(+ - )7.56μm),芦丁(IC50 = 294(+ - )0.56μm)。 然而,它对PC-3细胞系无毒。 结论是,2,4-二羟基,5-甲氧基 - 肉桂酸具有抗饱和潜力,其通过其抗氧化活性进一步增强,因此为有效管理糖尿病提供了理想的自然治疗选择。

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