辣木科潜在抗新城疫病毒类药物化合物的计算机分析

IF 2.1 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Muhammad Hammad Mustafa , Fayyaz-ur Rehman , Muhammad Ali , Mohsin Javed , Nazir Ahmad , Tayyaba Shafique , Ammar Zidan , Ali Bahadur , Shahid Iqbal , Sajid Mahmood , Abd-ElAziem Farouk , Ibrahim Jafri
{"title":"辣木科潜在抗新城疫病毒类药物化合物的计算机分析","authors":"Muhammad Hammad Mustafa ,&nbsp;Fayyaz-ur Rehman ,&nbsp;Muhammad Ali ,&nbsp;Mohsin Javed ,&nbsp;Nazir Ahmad ,&nbsp;Tayyaba Shafique ,&nbsp;Ammar Zidan ,&nbsp;Ali Bahadur ,&nbsp;Shahid Iqbal ,&nbsp;Sajid Mahmood ,&nbsp;Abd-ElAziem Farouk ,&nbsp;Ibrahim Jafri","doi":"10.1016/j.steroids.2025.109628","DOIUrl":null,"url":null,"abstract":"<div><div>Newcastle disease virus (NDV) classified in the <em>Avian avulavirus 1</em> [genus <em>Orthoavulavirus</em>, subfamily <em>Avulavirinae</em>, family <em>Paramyxoviridae</em>] constitutes a serious financial risk to the global poultry market. Available vaccines do not show good results in catering to the virus. Currently there is no FDA-approved drug to treat the disease. Nucleoprotein (NP) is a structural protein playing that constitutes a serious financial risk to the global poultry market.a valuable role in the virus replication process and encapsidation. This study is an effort to screen phytochemicals, from the plant family Moringaceae, as potential inhibitors of the N protein. ADMET (adsorption, distribution, metabolism, excretion and toxicity) analysis was performed to screen potential phytochemicals with drug likeliness. Molecular Docking was performed for the binding affinities. Gas Chromatography-Mass Spectrometry (GC–MS) and Density Function Theory (DFT) were performed to evaluate the phytochemicals bioavailability and reactivity, respectively. The stability of protein–ligand complexes was examined by 50 ns MD simulations and MM/PBSA values were calculated. Out of 128 phytochemicals, 22 phytochemicals were selected following ADMET screening. Based on the binding energies and the number of H bonding the following 10 phytochemicals were suggested as potential inhibitors to N protein of NDV – <em>cis</em>-11,14-eicosadienoic acid methyl ester, aurantiamide acetate, α-tocopherol, 4,8,12,16-tetramethylheptadecan-4-olide, 3,7,11,15-tetramethyl-2-hexadecen-1-ol, β-amyrin, β-sitosterol-3-O-β-<span>d</span>-galactopyranoside, α-amyrin, pterygospermin and sitogluside. Furthermore, DFT results showed that the 4 pytochemicals – <em>Cis</em>-11,14-eicosadienoic acid methyl ester, aurantiamide acetate, α-tocopherol, and 3,7,11,15-tetramethyl-2-hexadecen-1-ol were most reactive and thus could be used as potential inhibitors of NDV N protein. Further studies are required to validate the selected four phytochemicals as drug candidates against NDV.</div></div>","PeriodicalId":21997,"journal":{"name":"Steroids","volume":"219 ","pages":"Article 109628"},"PeriodicalIF":2.1000,"publicationDate":"2025-05-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"In silico analysis of Moringaceae derived potential drug-like compounds against Newcastle disease virus\",\"authors\":\"Muhammad Hammad Mustafa ,&nbsp;Fayyaz-ur Rehman ,&nbsp;Muhammad Ali ,&nbsp;Mohsin Javed ,&nbsp;Nazir Ahmad ,&nbsp;Tayyaba Shafique ,&nbsp;Ammar Zidan ,&nbsp;Ali Bahadur ,&nbsp;Shahid Iqbal ,&nbsp;Sajid Mahmood ,&nbsp;Abd-ElAziem Farouk ,&nbsp;Ibrahim Jafri\",\"doi\":\"10.1016/j.steroids.2025.109628\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Newcastle disease virus (NDV) classified in the <em>Avian avulavirus 1</em> [genus <em>Orthoavulavirus</em>, subfamily <em>Avulavirinae</em>, family <em>Paramyxoviridae</em>] constitutes a serious financial risk to the global poultry market. Available vaccines do not show good results in catering to the virus. Currently there is no FDA-approved drug to treat the disease. Nucleoprotein (NP) is a structural protein playing that constitutes a serious financial risk to the global poultry market.a valuable role in the virus replication process and encapsidation. This study is an effort to screen phytochemicals, from the plant family Moringaceae, as potential inhibitors of the N protein. ADMET (adsorption, distribution, metabolism, excretion and toxicity) analysis was performed to screen potential phytochemicals with drug likeliness. Molecular Docking was performed for the binding affinities. Gas Chromatography-Mass Spectrometry (GC–MS) and Density Function Theory (DFT) were performed to evaluate the phytochemicals bioavailability and reactivity, respectively. The stability of protein–ligand complexes was examined by 50 ns MD simulations and MM/PBSA values were calculated. Out of 128 phytochemicals, 22 phytochemicals were selected following ADMET screening. Based on the binding energies and the number of H bonding the following 10 phytochemicals were suggested as potential inhibitors to N protein of NDV – <em>cis</em>-11,14-eicosadienoic acid methyl ester, aurantiamide acetate, α-tocopherol, 4,8,12,16-tetramethylheptadecan-4-olide, 3,7,11,15-tetramethyl-2-hexadecen-1-ol, β-amyrin, β-sitosterol-3-O-β-<span>d</span>-galactopyranoside, α-amyrin, pterygospermin and sitogluside. Furthermore, DFT results showed that the 4 pytochemicals – <em>Cis</em>-11,14-eicosadienoic acid methyl ester, aurantiamide acetate, α-tocopherol, and 3,7,11,15-tetramethyl-2-hexadecen-1-ol were most reactive and thus could be used as potential inhibitors of NDV N protein. Further studies are required to validate the selected four phytochemicals as drug candidates against NDV.</div></div>\",\"PeriodicalId\":21997,\"journal\":{\"name\":\"Steroids\",\"volume\":\"219 \",\"pages\":\"Article 109628\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2025-05-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Steroids\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0039128X25000698\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Steroids","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0039128X25000698","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

新城疫病毒(NDV)属禽阿武拉病毒1[原阿武拉病毒属,阿武拉病毒亚科,副粘病毒科],对全球家禽市场构成严重的金融风险。现有疫苗在适应病毒方面没有显示出良好的效果。目前还没有fda批准的治疗这种疾病的药物。核蛋白(NP)是一种结构蛋白,对全球家禽市场构成严重的金融风险。在病毒复制过程和封装过程中发挥重要作用。本研究旨在筛选辣木科植物中可能抑制N蛋白的化学物质。ADMET(吸附、分布、代谢、排泄和毒性)分析筛选具有药物可能性的潜在植物化学物质。结合亲和度进行分子对接。采用气相色谱-质谱(GC-MS)和密度泛函理论(DFT)分别评价植物化学物质的生物利用度和反应性。通过50 ns MD模拟检测了蛋白质-配体复合物的稳定性,并计算了MM/PBSA值。在128种植物化学物质中,通过ADMET筛选选择了22种植物化学物质。根据结合能和H键的数目,提出了以下10种植物化学物质作为新冠病毒N蛋白的潜在抑制剂:顺式-11,14-二十碳二烯酸甲酯、醋酸金酰胺、α-生育酚、4,8,12,16-四甲基十七烷-4-内酯、3,7,11,15-四甲基-2-十六烯-1-醇、β-amyrin、β-谷甾醇-3- o -β-d-半乳糖苷、α-amyrin、pterygospermin和sitogluside。此外,DFT结果表明,顺式-11,14-二十二烯酸甲酯、醋酸金酰胺、α-生育酚和3,7,11,15-四甲基-2-十六烯-1-醇4种化学物质的活性最强,可以作为NDV N蛋白的潜在抑制剂。需要进一步的研究来验证所选的四种植物化学物质作为抗NDV的候选药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

In silico analysis of Moringaceae derived potential drug-like compounds against Newcastle disease virus

In silico analysis of Moringaceae derived potential drug-like compounds against Newcastle disease virus
Newcastle disease virus (NDV) classified in the Avian avulavirus 1 [genus Orthoavulavirus, subfamily Avulavirinae, family Paramyxoviridae] constitutes a serious financial risk to the global poultry market. Available vaccines do not show good results in catering to the virus. Currently there is no FDA-approved drug to treat the disease. Nucleoprotein (NP) is a structural protein playing that constitutes a serious financial risk to the global poultry market.a valuable role in the virus replication process and encapsidation. This study is an effort to screen phytochemicals, from the plant family Moringaceae, as potential inhibitors of the N protein. ADMET (adsorption, distribution, metabolism, excretion and toxicity) analysis was performed to screen potential phytochemicals with drug likeliness. Molecular Docking was performed for the binding affinities. Gas Chromatography-Mass Spectrometry (GC–MS) and Density Function Theory (DFT) were performed to evaluate the phytochemicals bioavailability and reactivity, respectively. The stability of protein–ligand complexes was examined by 50 ns MD simulations and MM/PBSA values were calculated. Out of 128 phytochemicals, 22 phytochemicals were selected following ADMET screening. Based on the binding energies and the number of H bonding the following 10 phytochemicals were suggested as potential inhibitors to N protein of NDV – cis-11,14-eicosadienoic acid methyl ester, aurantiamide acetate, α-tocopherol, 4,8,12,16-tetramethylheptadecan-4-olide, 3,7,11,15-tetramethyl-2-hexadecen-1-ol, β-amyrin, β-sitosterol-3-O-β-d-galactopyranoside, α-amyrin, pterygospermin and sitogluside. Furthermore, DFT results showed that the 4 pytochemicals – Cis-11,14-eicosadienoic acid methyl ester, aurantiamide acetate, α-tocopherol, and 3,7,11,15-tetramethyl-2-hexadecen-1-ol were most reactive and thus could be used as potential inhibitors of NDV N protein. Further studies are required to validate the selected four phytochemicals as drug candidates against NDV.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Steroids
Steroids 医学-内分泌学与代谢
CiteScore
5.10
自引率
3.70%
发文量
120
审稿时长
73 days
期刊介绍: STEROIDS is an international research journal devoted to studies on all chemical and biological aspects of steroidal moieties. The journal focuses on both experimental and theoretical studies on the biology, chemistry, biosynthesis, metabolism, molecular biology, physiology and pharmacology of steroids and other molecules that target or regulate steroid receptors. Manuscripts presenting clinical research related to steroids, steroid drug development, comparative endocrinology of steroid hormones, investigations on the mechanism of steroid action and steroid chemistry are all appropriate for submission for peer review. STEROIDS publishes both original research and timely reviews. For details concerning the preparation of manuscripts see Instructions to Authors, which is published in each issue of the journal.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信