Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Nat Prod Res. 2013;27(10):896-9. doi: 10.1080/14786419.2012.665913. Epub 2012 Mar 2.
In this study, we investigated tyrosinase inhibitory and radical scavenger activities of the hydroalcoholic extract from Peucedanum knappii Bornm aerial parts, together with its fractions. The EtOAc fraction showed the highest antioxidant and anti-tyrosinase activity was selected for the isolation and identification of major active compound(s). Two flavonol glycosides, named rhamnetin-3-O-β-D-glucopyranoside (1) and isorhamnetin-3-O-β-D-glucopyranoside (2) were isolated from the EtOAc fraction. Compound 1 showed the most active radical scavenging and potential anti-tyrosinase activity with SC50 values of 2.9 µg mL(-1) on the DPPH test and IC50 27.95 µg mL(-1) in mushroom tyrosinase method. Therefore, isolated flavonoids from P. knappii can be considered as antioxidant and effective tyrosinase inhibitors.
在这项研究中,我们研究了荆芥地上部分的水醇提取物及其馏分的酪氨酸酶抑制和自由基清除活性。乙酸乙酯馏分显示出最高的抗氧化和抗酪氨酸酶活性,因此被选择用于主要活性化合物的分离和鉴定。从乙酸乙酯馏分中分离得到两种黄酮醇糖苷,命名为鼠李素-3-O-β-D-吡喃葡萄糖苷(1)和异鼠李素-3-O-β-D-吡喃葡萄糖苷(2)。化合物 1 在 DPPH 试验中表现出最活跃的自由基清除和潜在的抗酪氨酸酶活性,SC50 值为 2.9 µg mL(-1),在蘑菇酪氨酸酶法中 IC50 值为 27.95 µg mL(-1)。因此,从荆芥中分离得到的类黄酮可以被认为是抗氧化剂和有效的酪氨酸酶抑制剂。