超越嘌呤能信号:多靶点药物发现的双配体方法。

IF 7.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Beatrice Francucci, Aleksei Smirnov, Andrea Spinaci, Michela Buccioni, Gabriella Marucci
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引用次数: 0

摘要

嘌呤能受体是治疗目前被认为无法治愈的许多多因素疾病的一个有吸引力的靶点。结合嘌呤能受体的多靶点药物在几种疾病的临床前研究中显示出相当大的前景。大多数目前尚无治疗方法的多因素病理是药学界面临的最大挑战。同时指向多个目标的分子可以抵消生物系统的典型冗余现象,并避免与药物鸡尾酒相关的副作用。本文综述了能够与嘌呤能受体和其他g蛋白偶联受体或酶相互作用的最重要的双配体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Beyond purinergic signaling: Dual ligand approaches to multitarget drug discovery

Beyond purinergic signaling: Dual ligand approaches to multitarget drug discovery
Purinergic receptors represent an attractive target for treating numerous multifactorial diseases currently considered incurable. Multitargeted agents binding purinergic receptors show considerable promise in preclinical studies in several diseases. Most of the multifactorial pathologies for which no therapy is currently known represent the greatest challenge for the pharmaceutical community. Molecules directed simultaneously toward multiple targets could counteract the redundancy phenomena typical of biological systems and avoid the side effects associated with drug cocktails. This review is intended to provide a summary of the most significant dual ligands able to interact with purinergic receptors and other G-protein-coupled receptors or enzymes.
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来源期刊
Drug Discovery Today
Drug Discovery Today 医学-药学
CiteScore
14.80
自引率
2.70%
发文量
293
审稿时长
6 months
期刊介绍: Drug Discovery Today delivers informed and highly current reviews for the discovery community. The magazine addresses not only the rapid scientific developments in drug discovery associated technologies but also the management, commercial and regulatory issues that increasingly play a part in how R&D is planned, structured and executed. Features include comment by international experts, news and analysis of important developments, reviews of key scientific and strategic issues, overviews of recent progress in specific therapeutic areas and conference reports.
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