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发现巴拉克菌素及其衍生物作为新型抗病毒和杀真菌剂。

Discovery of Barakacin and Its Derivatives as Novel Antiviral and Fungicidal Agents.

机构信息

Tianjin Key Laboratory of Structure and Performance for Functional Molecules, College of Chemistry, Tianjin Normal University, Tianjin 300387, China.

School of Chemical Engineering and Technology, Hebei University of Technology, Tianjin 300401, China.

出版信息

Molecules. 2023 Mar 29;28(7):3032. doi: 10.3390/molecules28073032.

Abstract

Pesticides are essential for the development of agriculture. It is urgent to develop green, safe and efficient pesticides. Bisindole alkaloids have unique and concise structures and broad biological activities, which make them an important leading skeleton in the creation of new pesticides. In this work, we synthesized bisindole alkaloid barakacin in a simple seven-step process, and simultaneously designed and synthesized a series of its derivatives. Biological activity research indicated that most of these compounds displayed good antiviral activities against tobacco mosaic virus (TMV). Among them, compound exerted a superior inhibitory effect in comparison to commercially available antiviral agent ribavirin, and could be expected to become a novel antiviral candidate. Molecular biology experiments and molecular docking research found that the potential target of compound was TMV coat protein (CP). These compounds also showed broad-spectrum anti-fungal activities against seven kinds of plant fungi.

摘要

农药对于农业发展至关重要。开发绿色、安全、高效的农药迫在眉睫。双吲哚生物碱具有独特而简洁的结构和广泛的生物活性,使它们成为创制新型农药的重要先导骨架。在这项工作中,我们通过简单的七步合成法合成了双吲哚生物碱巴卡辛,并同时设计和合成了一系列其衍生物。生物活性研究表明,这些化合物大多数对烟草花叶病毒(TMV)表现出良好的抗病毒活性。其中,化合物对市售抗病毒剂利巴韦林表现出优越的抑制效果,有望成为一种新型的抗病毒候选药物。分子生物学实验和分子对接研究发现,化合物的潜在靶标是 TMV 外壳蛋白(CP)。这些化合物还对七种植物真菌表现出广谱的抗真菌活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd77/10095642/f8ce23a060ce/molecules-28-03032-g001.jpg

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