Highly Oxygenated Cyclobutane Ring in Biomolecules: Insights into Structure and Activity

Oxygen Pub Date : 2024-05-22 DOI:10.3390/oxygen4020012
Valery M. Dembitsky
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Abstract

This review explores the unique structural and functional characteristics of natural products featuring highly oxygenated cyclobutane rings, with a specific focus on oxetane and 1,2-dioxetane motifs. It presents the structures and biological activities of compounds containing these rings, highlighting their contribution to molecular stability and pharmacological potency. Through detailed case studies and recent research findings, it has been demonstrated that these oxygen-rich rings enhance the molecular diversity and biological efficacy of natural products, potentially offering new avenues for drug development. Notably, these compounds are predominantly synthesized by microorganisms and can also be found in extracts from fungi, plants, and certain marine invertebrates. Compounds with oxetane and 1,2-dioxetane rings are primarily noted for their strong antineoplastic properties, among other biological activities. In contrast, most 1,2-dioxetanes exhibit potent antiprotozoal effects. It is important to note that 1,2-dioxetanes often serve as intermediate products in oxidation reactions, characterized by their instability and propensity to decompose into new compounds.
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生物大分子中的高氧环丁烷环:洞察结构与活性
这篇综述探讨了以高含氧环丁烷环为特征的天然产物的独特结构和功能特性,特别关注氧杂环丁烷和 1,2-dioxetane 主题。该书介绍了含有这些环的化合物的结构和生物活性,强调了它们对分子稳定性和药效的贡献。通过详细的案例研究和最新的研究发现,这些富氧环增强了天然产品的分子多样性和生物功效,可能为药物开发提供新的途径。值得注意的是,这些化合物主要由微生物合成,也可在真菌、植物和某些海洋无脊椎动物的提取物中发现。具有氧杂环和 1,2-二氧杂环的化合物主要具有很强的抗肿瘤特性和其他生物活性。相比之下,大多数 1,2-二氧杂环丁烷具有很强的抗原虫作用。值得注意的是,1,2-二氧杂环丁烷通常是氧化反应的中间产物,其特点是不稳定,容易分解成新的化合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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