Department of Pharmacy, University of Peshawar , Peshawar , Pakistan.
J Enzyme Inhib Med Chem. 2013 Oct;28(5):997-1001. doi: 10.3109/14756366.2012.702344. Epub 2012 Jul 18.
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 µM. The antioxidant property of the compound was compared with α-tocopherole and vitamin C having IC50 values 96 ± 0.46 and 90 ± 0.56 µM, respectively. In case of antiglycation assay, the compound exhibited moderate activity (IC50 = 355 ± 7.56 µM) similar to standard compound, rutin (IC50 = 294 ± 0.56 µM). 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.
从紫堇属植物全草中分离得到一种新的肉桂酸衍生物,为灰白色针状结晶。根据包括高分辨电喷雾电离质谱(HREI-MS)和 1D 和 2D NMR 在内的各种现代光谱技术,其结构被阐明为 2,4-二羟基-5-甲氧基肉桂酸。它对 DPPH(二苯基-2-苦基肼基)自由基显示出明显的抑制作用,IC50 = 124 ± 5.76 μM。该化合物的抗氧化性能与 α-生育酚和维生素 C 进行了比较,其 IC50 值分别为 96 ± 0.46 和 90 ± 0.56 μM。在抗糖化试验中,该化合物表现出中等活性(IC50 = 355 ± 7.56 μM),与标准化合物芦丁(IC50 = 294 ± 0.56 μM)相似。然而,它对 PC-3 细胞系没有毒性。结论是 2,4-二羟基-5-甲氧基肉桂酸具有抗糖化潜力,其抗氧化活性进一步增强,从而为有效管理糖尿病提供了一种理想的天然治疗选择。