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首页> 外文期刊>Bioorganic and medicinal chemistry >New insights into highly potent tyrosinase inhibitors based on 3-heteroarylcoumarins: Anti-melanogenesis and antioxidant activities, and computational molecular modeling studies
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New insights into highly potent tyrosinase inhibitors based on 3-heteroarylcoumarins: Anti-melanogenesis and antioxidant activities, and computational molecular modeling studies

机译:基于3-杂芳族毒素的高效酪氨酸酶抑制剂的新见解:抗糖胺发生和抗氧化活性,以及计算分子建模研究

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Melanogenesis is a physiological pathway for the formation of melanin. Tyrosinase catalyzes the first step of this process and down-regulation of its activity is responsible for the inhibition of melanogenesis. The search for molecules capable of controlling hyperpigmentation is a trend topic in health and cosmetics. A series of heteroarylcoumarins have been synthesized and evaluated. Compounds 4 and 8 exhibited higher tyrosinase inhibitory activities (IC50 = 0.15 and 0.38 mu M, respectively), than the reference compound, kojic acid (IC50 = 17.9 mu M). Compound 4 acts as competitive, while compound 8 as uncompetitive inhibitor of mushroom tyrosinase. Furthermore, compounds 2 and 8 inhibited tyrosinase activity and melanin production in B16F10 cells. In addition, compounds 2-4 and 8 proved to have an interesting antioxidant profile in both ABTS and DPPH radicals scavenging assays. Docking experiments were carried out in order to study the interactions between these heteroarylcoumarins and mushroom tyrosinase. (C) 2017 Elsevier Ltd. All rights reserved.
机译:黑糖素是形成黑色素的生理途径。酪氨酸酶催化该过程的第一步和对其活性的下调是负责抑制黑色发生的抑制作用。寻找能够控制超差异化的分子是健康和化妆品的趋势话题。已经合成和评估了一系列杂芳族草林。化合物4和8表现出较高的酪氨酸酶抑制活性(IC50 = 0.15和0.38μm),而不是参考化合物,Kojic酸(IC50 =17.9μm)。化合物4用作竞争力,而化合物8作为蘑菇酪氨酸酶的非竞争力抑制剂。此外,化合物2和8抑制B16F10细胞中的酪氨酸酶活性和黑色素产生。此外,化合物2-4和8证明在ABTS和DPPH基团中具有有趣的抗氧化曲线清除测定。进行对接实验,以研究这些杂芳族毒素和蘑菇酪氨酸酶之间的相互作用。 (c)2017 Elsevier Ltd.保留所有权利。

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