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天然存在的和合成的咪唑类化合物:它们的化学性质及其生物活性。

Naturally occurring and synthetic imidazoles: their chemistry and their biological activities.

作者信息

De Luca Lidia

机构信息

Dipartimento di Chimica, Via Vienna 2, Sassari (07100), Italy.

出版信息

Curr Med Chem. 2006;13(1):1-23.

Abstract

Imidazoles are an important class of heterocycles and include many substances of both biological and chemical interest. They are part of a large number of highly significant biomolecules such as the essential amino acid histidine and related compounds, biotin, and the imidazole alkaloids. Insertion of the imidazole nucleus is an important synthetic strategy in drug discovery. Imidazole drugs have broad applications in many areas of clinical medicine. The imidazoles are a class of antifungal azole derivatives and have a broad spectrum of activities both in vitro and in vivo. The imidazole moiety is also contained in many histaminergic ligands for histamine H1, H2, and H3 receptors. These are currently used as tools in pharmacological studies. The important therapeutic properties of imidazole related drugs have encouraged the medicinal chemists to synthesize and test a large number of novel molecules. Some of these have chemotherapeutic properties, such as for example several FTase inhibitors with an imidazole moiety. Imidazole derivatives have also been shown to have antibacterial activity and recently several P38 MAP Kinase inhibitors and 5-Lipoxygenase inhibitors containing the imidazole moiety have been synthesized. This review reports current progress in the area of new biologically active imidazoles and recently discovered naturally occurring imidazole.

摘要

咪唑是一类重要的杂环化合物,包含许多具有生物学和化学意义的物质。它们是大量极具重要性的生物分子的组成部分,如必需氨基酸组氨酸及相关化合物、生物素和咪唑生物碱。在药物研发中,引入咪唑环是一种重要的合成策略。咪唑类药物在临床医学的许多领域都有广泛应用。咪唑类是一类抗真菌唑衍生物,在体外和体内均具有广泛的活性。许多组胺H1、H2和H3受体的组胺能配体中也含有咪唑部分。这些目前在药理学研究中用作工具。咪唑相关药物的重要治疗特性促使药物化学家合成并测试了大量新型分子。其中一些具有化疗特性,例如几种含咪唑部分的法尼基转移酶(FTase)抑制剂。咪唑衍生物也已显示出抗菌活性,最近还合成了几种含咪唑部分的P38丝裂原活化蛋白激酶(MAP Kinase)抑制剂和5-脂氧合酶抑制剂。本综述报道了新型生物活性咪唑领域的当前进展以及最近发现的天然存在的咪唑。

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