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新型戊二酸衍生物在药物化学中的应用。

Squaric acid analogues in medicinal chemistry.

机构信息

Department of Organic Chemistry, Faculty of Science, Palacky University Olomouc, 17. listopadu 12, 771 46, Olomouc, Czech Republic.

Medicinal Chemistry, Institute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University in Olomouc, Hněvotínská 5, 779 00, Olomouc, Czech Republic.

出版信息

Eur J Med Chem. 2021 Jan 1;209:112872. doi: 10.1016/j.ejmech.2020.112872. Epub 2020 Oct 2.

Abstract

In this review, we summarize the published data on squaric acid analogues with a special focus on their use in medicinal chemistry and as potential drugs. Squaric acid is an interesting small molecule with an almost perfectly square shape, and its analogues have a variety of biological activities that are enabled by the presence of significant H-bond donors and acceptors. Unfortunately, most of these compounds also exhibit reactive functionalities, and this deters the majority of medicinal chemists and pharmacologists from trying to use them in drug development. However, this group of compounds is experiencing a renaissance, and large numbers of them are being tested for antiprotozoal, antibacterial, antifungal, and antiviral activities. The most useful of these compounds exhibited IC values in the nanomolar range, which makes them promising drug candidates. In addition to these activities, their interactions with living systems were intensively explored, revealing that squaric acid analogues inhibit various enzymes and often serve as receptor antagonists and that the squaric acid moiety may be used as a non-classical isosteric replacement for other functional groups such as carboxylate. In summary, this review is focused on squaric acid and its analogues and their use in medicinal chemistry and should serve as a guide for other researchers in the field to demonstrate the potential of these compounds based on previous research.

摘要

在这篇综述中,我们总结了已发表的关于丁烷二酸类似物的资料,特别关注它们在药物化学中的应用和作为潜在药物的潜力。丁烷二酸是一种具有几乎完美正方形形状的有趣小分子,其类似物具有多种生物学活性,这得益于其存在大量氢键供体和受体。不幸的是,这些化合物中的大多数也表现出反应性官能团,这使得大多数药物化学家和药理学家不愿尝试将其用于药物开发。然而,这一类化合物正在经历复兴,大量的化合物正在被测试其抗原生动物、抗菌、抗真菌和抗病毒活性。其中最有用的化合物在纳摩尔范围内表现出 IC 值,这使它们成为有前途的候选药物。除了这些活性,它们与生命系统的相互作用也被深入研究,揭示了丁烷二酸类似物抑制各种酶,并且常常作为受体拮抗剂,并且丁烷二酸部分可以用作其他功能团的非经典等排体,例如羧酸酯。总之,这篇综述集中于丁烷二酸及其类似物及其在药物化学中的应用,应作为该领域其他研究人员的指南,以展示基于先前研究的这些化合物的潜力。

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