天然酚酸作为抗自由基和抗菌药物的两步流动酰胺化研究。

IF 3.3 2区 生物学 Q2 CHEMISTRY, MEDICINAL
Journal of Natural Products Pub Date : 2025-05-23 Epub Date: 2025-03-31 DOI:10.1021/acs.jnatprod.5c00131
Desirée Pecora, Anna M Magni, Sara Vicinanza, Francesca Annunziata, Salvatore Princiotto, Silvia Donzella, Gabriele Meroni, Piera A Martino, Nicoletta Basilico, Silvia Parapini, Paola Conti, Chiara Borsari, Lucia Tamborini
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引用次数: 0

摘要

天然羟基肉桂酸酰胺(HCAAs)和河岸素提供显著的健康益处。然而,从自然资源中提取它们是困难的,传统的合成方法仍然是浪费的,因此需要更有效的替代品。本研究建立了一种两步化学-酶流动法,用于酚酸的高效酯化和酰胺化,并成功地应用于利帕林衍生物和HCAAs的合成。以香草酸为模型起始原料,以硅酸钡(SCX-3)为固定化酸催化剂,优化了流动Fischer酯化反应,在短停留时间内获得了定量产率。以固定化南极念珠菌脂肪酶B为催化剂,在甲苯条件下进行酰胺化反应,得到了所需的酰胺。合成的化合物具有清除自由基、抗菌和抗利什曼原虫的特性。总的来说,这项工作揭示了一种新的方法,有效地合成河岸河岸素衍生物和具有有趣的生物学特性的HCAAs。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Two-Step Flow Amidation of Natural Phenolic Acids as Antiradical and Antimicrobial Agents.

Natural hydroxycinnamic acid amides (HCAAs) and riparins offer significant health benefits. However, their extraction from natural sources is difficult, and traditional synthetic methods remain wasteful, raising the need for more efficient alternatives. In this work, a two-step chemo-enzymatic flow method for the efficient esterification and amidation of phenolic acids was developed and successfully applied to the synthesis of riparin derivatives and HCAAs. The flow Fischer esterification was optimized using vanillic acid as a model starting material and SiliaBond Tosic Acid (SCX-3) as an immobilized acid catalyst, achieving a quantitative yield in a short residence time. The following amidation step, catalyzed by immobilized Candida antarctica lipase B, was optimized in toluene, leading to the desired amides. The synthesized compounds were evaluated for their radical scavenging, antibacterial, and antileishmanial properties. Overall, this work disclosed a novel approach for the efficient synthesis of riparin derivatives and HCAAs with interesting biological properties.

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来源期刊
CiteScore
9.10
自引率
5.90%
发文量
294
审稿时长
2.3 months
期刊介绍: The Journal of Natural Products invites and publishes papers that make substantial and scholarly contributions to the area of natural products research. Contributions may relate to the chemistry and/or biochemistry of naturally occurring compounds or the biology of living systems from which they are obtained. Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin. When new compounds are reported, manuscripts describing their biological activity are much preferred. Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.
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