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黄烷醇类在 L.中的结构、合成与生物活性。

Xanthanolides in L.: Structures, Synthesis and Bioactivity.

机构信息

Department of Applied Chemistry, Chemistry and Chemical Engineering College, Xinjiang Agricultural University, Urumqi 830052, China.

Institute for Drug Control of Xinjiang Uygur Autonomous Region, Urumqi 830054, China.

出版信息

Molecules. 2022 Nov 22;27(23):8136. doi: 10.3390/molecules27238136.

Abstract

Xanthanolides were particularly characteristic of the genus , which exhibited broad biological effects and have drawn much attention in pharmacological application. The review surveyed the structures and bioactivities of the xanthanolides in the genus , and summarized the synthesis tactics of xanthanolides. The results indicated that over 30 naturally occurring xanthanolides have been isolated from the genus in monomeric, dimeric and trimeric forms. The bioassay-guided fractionation studies suggested that the effective fractions on antitumor activities were mostly from weak polar solvents, and xanthatin () was the most effective and well-studied xanthanolide. The varieties of structures and structure-activity relationships of the xanthanolides had provided the promising skeleton for the further study. The review aimed at providing guidance for the efficient preparation and the potential prospects of the xanthanolides in the medicinal industry.

摘要

黄烷醇内酯类化合物是该属的特征成分,具有广泛的生物活性,在药理学应用中引起了广泛关注。本文综述了该属黄烷醇内酯类化合物的结构和生物活性,并总结了黄烷醇内酯类化合物的合成策略。结果表明,从该属中已分离出 30 多种单体、二聚体和三聚体形式的天然黄烷醇内酯类化合物。生物活性导向的分步分离研究表明,具有抗肿瘤活性的有效部位主要来自弱极性溶剂,黄烷酮()是研究最为充分、最有效的黄烷醇内酯类化合物。黄烷醇内酯类化合物结构的多样性及其与结构活性关系为进一步研究提供了有前途的骨架。本文旨在为黄烷醇内酯类化合物在医药工业中的高效制备和潜在前景提供指导。

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