植物物质是原始抗病毒药物的潜在来源

S. Adekenov, Karaganda Kazakhstan Production Holding “Phytochemistry”
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引用次数: 1

摘要

本文综述了萜类化合物、黄酮类化合物、生物碱类化合物的研究进展及相关文献资料。以倍半萜类γ-内酯精氨酸、毛豆素和α-三冬氨酸为原料合成了新的双分子衍生物和酮酰胺衍生物,产率高达80%。采用分子对接方法研究天然化合物及其衍生物与SARS-Cov-2的“构效”关系。结果表明,倍半萜γ-内酯及其衍生物对SARS-Cov-2刺突蛋白和蛋白酶以及血管紧张素转换酶2具有抑制作用。所鉴定的分子可作为候选分子,在其基础上开发具有抗病毒活性的新药。
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PLANT SUBSTANCES AS POTENTIAL SOURCE OF ORIGINAL ANTI-VIRUS AGENTS
This article summarizes the literature data and the results of our own studies on the search for antiviral compounds based on terpenoids, flavonoids, alkaloids. New bimolecular and ketoamide derivatives based on sesquiterpene γ-lactones arglabin, grossheimin and α-santonin were synthesized in quantitative yields up to 80%. The molecular docking method was used to study the “structure-activity” relationship of natural compounds and their derivatives in relation to SARS-Cov-2. The results obtained in silico demonstrated that sesquiterpene γ-lactones and their derivatives inhibit the SARS-Cov-2 spike protein and proteases, as well as the angiotensin-converting enzyme 2. The identified molecules can be considered as candidates for the development of new drugs with antiviral activity on their basis.
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