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石蒜科生物碱作为潜在的糖原合成酶激酶-3β抑制剂。

Amaryllidaceae Alkaloids as Potential Glycogen Synthase Kinase-3β Inhibitors.

机构信息

ADINACO Research Group, Department of Pharmacognosy, Faculty of Pharmacy, Charles University, 500 05 Hradec Králové, Czech Republic.

Department of Pharmaceutical Botany, Faculty of Pharmacy, Charles University, 500 05 Hradec Králové, Czech Republic.

出版信息

Molecules. 2018 Mar 21;23(4):719. doi: 10.3390/molecules23040719.

Abstract

Glycogen synthase kinase-3β (GSK-3β) is a multifunctional serine/threonine protein kinase that was originally identified as an enzyme involved in the control of glycogen metabolism. It plays a key role in diverse physiological processes including metabolism, the cell cycle, and gene expression by regulating a wide variety of well-known substances like glycogen synthase, tau-protein, and β-catenin. Recent studies have identified GSK-3β as a potential therapeutic target in Alzheimer´s disease, bipolar disorder, stroke, more than 15 types of cancer, and diabetes. GSK-3β is one of the most attractive targets for medicinal chemists in the discovery, design, and synthesis of new selective potent inhibitors. In the current study, twenty-eight Amaryllidaceae alkaloids of various structural types were studied for their potency to inhibit GSK-3β. Promising results have been demonstrated by alkaloids of the homolycorine-{9--demethylhomolycorine (IC = 30.00 ± 0.71 µM), masonine (IC = 27.81 ± 0.01 μM)}, and lycorine-types {caranine (IC = 30.75 ± 0.04 μM)}.

摘要

糖原合酶激酶-3β(GSK-3β)是一种多功能丝氨酸/苏氨酸蛋白激酶,最初被鉴定为参与糖原代谢控制的酶。它通过调节糖原合酶、tau 蛋白和 β-连环蛋白等多种知名物质,在多种生理过程中发挥着关键作用,包括代谢、细胞周期和基因表达。最近的研究表明,GSK-3β 是阿尔茨海默病、双相情感障碍、中风、超过 15 种癌症和糖尿病的潜在治疗靶点。GSK-3β 是药物化学家在发现、设计和合成新型选择性强效抑制剂方面最具吸引力的目标之一。在本研究中,研究了 28 种不同结构类型的石蒜科生物碱对 GSK-3β 的抑制活性。具有潜在前景的生物碱包括 homolycorine -{9--demethylhomolycorine(IC = 30.00 ± 0.71 µM)、masonine(IC = 27.81 ± 0.01 μM)} 和 lycorine 型 {caranine(IC = 30.75 ± 0.04 μM)}。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc7b/6017564/f3338579f5f4/molecules-23-00719-g001.jpg

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