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用唑类药物靶向治疗糖尿病。

Targeting Diabetes with Azole-derived Medicinal Agents.

机构信息

Department of Pharmaceutical Chemistry, School of Pharmaceutical Sciences, Lovely Professional University, Jalandhar-Delhi G.T. Road (NH-1), Phagwara (Punjab) 144411, India.

出版信息

Med Chem. 2024;20(9):855-875. doi: 10.2174/0115734064289990240524055002.

Abstract

Azoles have long been regarded as an ideal scaffold for the development of numerous innovative therapeutic agents as well as other incredibly adaptable and beneficial chemicals with prospective uses in a variety of fields, including materials, energetics (explosophores), and catalysis (azole organocatalytic arbitration). Azoles exhibit promising pharmacological activities, including antimicrobial, antidiabetic, antiviral, antidepressant, antihistaminic, antitumor, antioxidant, antiallergic, antihelmintic, and antihypertensive activity. According to a database analysis of U.S. FDAapproved medications, 59% of specific medications are connected to small molecules that have heterocycles having nitrogen atoms. The azole moiety has impressive electron abundance. Azoles promptly attach to various receptors as well as enzymes in the physiological environment via distinct specialized interactions, contributing to their anti-diabetic potential. This review encompasses the recent research progress on potent azole-derived antidiabetic agents that can be used as an alternative for the management of type-2 diabetes.

摘要

唑类化合物长期以来一直被视为开发众多创新治疗药物的理想支架,以及其他具有多种潜在用途的适应性极强和有益的化学品,包括材料、能量学(爆炸物)和催化(唑类有机催化仲裁)。唑类化合物表现出有希望的药理学活性,包括抗菌、抗糖尿病、抗病毒、抗抑郁、抗组胺、抗肿瘤、抗氧化、抗过敏、抗寄生虫和抗高血压活性。根据美国 FDA 批准药物的数据库分析,59%的特定药物与具有含氮原子的杂环的小分子有关。唑部分具有令人印象深刻的电子丰度。唑类化合物通过独特的专门相互作用迅速与生理环境中的各种受体和酶结合,这有助于它们的抗糖尿病潜力。这篇综述涵盖了最近关于强效唑类衍生抗糖尿病药物的研究进展,这些药物可作为 2 型糖尿病管理的替代药物。

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