植物代谢物对猴痘病毒的治疗前景:一项计算机研究。

IF 1.1 Q4 VIROLOGY
Anik Banik, Sheikh Rashel Ahmed, Sonia Binte Shahid, Tufayel Ahmed, Hafaza Khandaker Tamanna, Hlamrasong Marma
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引用次数: 0

摘要

猴痘病毒在2022年5月仍在传播,第一例病例是在一名与尼日利亚有旅行关系的人中发现的。利用基于分子对接的技术,我们评估了从植物中获得的不同生物活性化学物质对猴痘病毒的有效性。共鉴定了56种植物化合物的抗猴痘能力,结果表明,前4种候选化合物具有比对照更高的结合亲和力。我们的目标是猴痘profile -like蛋白,它在病毒复制和组装中起关键作用。代谢产物中,姜黄素的结合亲和力最强,为-37.43 kcal/mol,其次是根茎素(-34.89 kcal/mol)、胡椒碱(-34.58 kcal/mol)和香豆素(-34.14 kcal/mol)。根据ADME和毒性评估,前四种物质没有负面影响。此外,四种化合物表现出抗变形性,这得到了正态分析的证实。根据生物活性预测研究,化合物靶点最高的是酶、膜受体和氧化还原酶。此外,该研究还发现,一种皂荚素类似物wortmannin可以表现得像一种正痘病毒。研究发现,这些具有生物活性的天然候选药物有可能作为猴痘病毒抑制剂。我们建议进一步的实验验证,以确认该研究的有希望的发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Therapeutic Promises of Plant Metabolites against Monkeypox Virus: An In Silico Study.

Therapeutic Promises of Plant Metabolites against Monkeypox Virus: An In Silico Study.

Therapeutic Promises of Plant Metabolites against Monkeypox Virus: An In Silico Study.

Therapeutic Promises of Plant Metabolites against Monkeypox Virus: An In Silico Study.

The monkeypox virus was still spreading in May 2022, with the first case identified in a person with travel ties to Nigeria. Using molecular docking-based techniques, we evaluated the efficiency of different bioactive chemicals obtained from plants against the monkeypox virus. A total of 56 plant compounds were evaluated for antimonekypox capabilities, with the top four candidates having a higher binding affinity than the control. We targeted the monkeypox profilin-like protein, which plays a key role in viral replication and assembly. Among the metabolites, curcumin showed the strongest binding affinity with a value of -37.43 kcal/mol, followed by gedunin (-34.89 kcal/mol), piperine (-34.58 kcal/mol), and coumadin (-34.14 kcal/mol). Based on ADME and toxicity assessments, the top four substances had no negative impacts. Furthermore, four compounds demonstrated resistance to deformability, which was corroborated by normal mode analysis. According to the bioactivity prediction study, the top compound target class was an enzyme, membrane receptor, and oxidoreductase. Furthermore, the study discovered that wortmannin, a gedunin analogue, can behave as an orthopoxvirus. The study found that these bioactive natural drug candidates could potentially work as monkeypox virus inhibitors. We recommended further experimental validation to confirm the promising findings of the study.

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来源期刊
CiteScore
2.30
自引率
0.00%
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23
审稿时长
22 weeks
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