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糖原合酶激酶3(GSK-3)抑制剂作为治疗糖尿病、神经退行性疾病、癌症和炎症的新型有前景药物。

Glycogen synthase kinase 3 (GSK-3) inhibitors as new promising drugs for diabetes, neurodegeneration, cancer, and inflammation.

作者信息

Martinez Ana, Castro Ana, Dorronsoro Isabel, Alonso Mercedes

机构信息

Instituto de Química Médica (CSIC), Juan de la Cierva 3, 28006 Madrid, Spain.

出版信息

Med Res Rev. 2002 Jul;22(4):373-84. doi: 10.1002/med.10011.

Abstract

Glycogen synthase kinase 3 (GSK-3) was initially described as a key enzyme involved in glycogen metabolism, but is now known to regulate a diverse array of cell functions. Two forms of the enzyme, GSK-3alpha and GSK-3beta, have been previously identified. Small molecules inhibitors of GSK-3 may, therefore, have several therapeutic uses, including the treatment of neurodegenerative diseases, diabetes type II, bipolar disorders, stroke, cancer, and chronic inflammatory disease. As there is lot of recent literature dealing with the involvement of GSK-3 in the molecular pathways of different diseases, this review is mainly focused on the new GSK-3 inhibitors discovered or specifically developed for this enzyme, their chemical structure, synthesis, and structure-activity relationships, with the aim to provide some clues for the future optimization of these promising drugs.

摘要

糖原合酶激酶3(GSK-3)最初被描述为参与糖原代谢的关键酶,但现在已知它能调节多种细胞功能。此前已鉴定出该酶的两种形式,即GSK-3α和GSK-3β。因此,GSK-3的小分子抑制剂可能有多种治疗用途,包括治疗神经退行性疾病、II型糖尿病、双相情感障碍、中风、癌症和慢性炎症性疾病。由于最近有大量文献探讨GSK-3参与不同疾病的分子途径,本综述主要关注为该酶发现或专门开发的新型GSK-3抑制剂、它们的化学结构、合成以及构效关系,旨在为这些有前景的药物的未来优化提供一些线索。

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