针对 SARS-CoV-2 的 NO-Sartans 的硅学评估。

Negar Omidkhah, Farzin Hadizadeh, Razieh Ghodsi, Prashant Kesharwani, Amirhossein Sahebkar
{"title":"针对 SARS-CoV-2 的 NO-Sartans 的硅学评估。","authors":"Negar Omidkhah, Farzin Hadizadeh, Razieh Ghodsi, Prashant Kesharwani, Amirhossein Sahebkar","doi":"10.2174/0115701638279362240223070810","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Numerous clinical trials are currently investigating the potential of nitric oxide (NO) as an antiviral agent against coronaviruses, including SARS-CoV-2. Additionally, some researchers have reported positive effects of certain Sartans against SARS-CoV-2.</p><p><strong>Method: </strong>Considering the impact of NO-Sartans on the cardiovascular system, we have compiled information on the general structure, synthesis methods, and biological studies of synthesized NOSartans. <i>In silico</i> evaluation of all NO-Sartans and approved sartans against three key SARS-CoV- -2 targets, namely M<sup>pro</sup> (PDB ID: 6LU7), NSP16 (PDB ID: 6WKQ), and ACE-2 (PDB ID: 1R4L), was performed using MOE.</p><p><strong>Results: </strong>Almost all NO-Sartans and approved sartans demonstrated promising results in inhibiting these SARS-CoV-2 targets. Compound 36 (CLC-1280) showed the best docking scores against the three evaluated targets and was further evaluated using molecular dynamics (MD) simulations.</p><p><strong>Conclusion: </strong>Based on our <i>in silico</i> studies, CLC-1280 (a Valsartan dinitrate) has the potential to be considered as an inhibitor of the SARS-CoV-2 virus. However, further <i>in vitro</i> and <i>in vivo</i> evaluations are necessary for the drug development process.</p>","PeriodicalId":93962,"journal":{"name":"Current drug discovery technologies","volume":" ","pages":"e050324227669"},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"<i>In silico</i> Evaluation of NO-Sartans against SARS-CoV-2.\",\"authors\":\"Negar Omidkhah, Farzin Hadizadeh, Razieh Ghodsi, Prashant Kesharwani, Amirhossein Sahebkar\",\"doi\":\"10.2174/0115701638279362240223070810\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Numerous clinical trials are currently investigating the potential of nitric oxide (NO) as an antiviral agent against coronaviruses, including SARS-CoV-2. Additionally, some researchers have reported positive effects of certain Sartans against SARS-CoV-2.</p><p><strong>Method: </strong>Considering the impact of NO-Sartans on the cardiovascular system, we have compiled information on the general structure, synthesis methods, and biological studies of synthesized NOSartans. <i>In silico</i> evaluation of all NO-Sartans and approved sartans against three key SARS-CoV- -2 targets, namely M<sup>pro</sup> (PDB ID: 6LU7), NSP16 (PDB ID: 6WKQ), and ACE-2 (PDB ID: 1R4L), was performed using MOE.</p><p><strong>Results: </strong>Almost all NO-Sartans and approved sartans demonstrated promising results in inhibiting these SARS-CoV-2 targets. Compound 36 (CLC-1280) showed the best docking scores against the three evaluated targets and was further evaluated using molecular dynamics (MD) simulations.</p><p><strong>Conclusion: </strong>Based on our <i>in silico</i> studies, CLC-1280 (a Valsartan dinitrate) has the potential to be considered as an inhibitor of the SARS-CoV-2 virus. However, further <i>in vitro</i> and <i>in vivo</i> evaluations are necessary for the drug development process.</p>\",\"PeriodicalId\":93962,\"journal\":{\"name\":\"Current drug discovery technologies\",\"volume\":\" \",\"pages\":\"e050324227669\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current drug discovery technologies\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2174/0115701638279362240223070810\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current drug discovery technologies","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/0115701638279362240223070810","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

导言:目前有许多临床试验正在研究一氧化氮(NO)作为抗冠状病毒(包括 SARS-CoV-2)药物的潜力。此外,一些研究人员还报告了某些沙坦类药物对 SARS-CoV-2 的积极作用:考虑到 NO-Sartans 对心血管系统的影响,我们汇编了有关合成 NOSartans 的一般结构、合成方法和生物学研究的信息。利用 MOE 对所有 NO-Sartans 和已批准的沙坦类药物针对三个关键的 SARS-CoV--2 靶点,即 Mpro(PDB ID:6LU7)、NSP16(PDB ID:6WKQ)和 ACE-2(PDB ID:1R4L)进行了硅学评估:结果:几乎所有 NO 沙坦类药物和已批准的沙坦类药物在抑制这些 SARS-CoV-2 靶点方面都表现出了良好的效果。化合物 36(CLC-1280)对三个评估靶点的对接得分最高,并通过分子动力学(MD)模拟进行了进一步评估:根据我们的硅学研究,CLC-1280(一种二硝酸缬沙坦)有可能被视为 SARS-CoV-2 病毒的抑制剂。然而,在药物开发过程中还需要进一步的体外和体内评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
In silico Evaluation of NO-Sartans against SARS-CoV-2.

Introduction: Numerous clinical trials are currently investigating the potential of nitric oxide (NO) as an antiviral agent against coronaviruses, including SARS-CoV-2. Additionally, some researchers have reported positive effects of certain Sartans against SARS-CoV-2.

Method: Considering the impact of NO-Sartans on the cardiovascular system, we have compiled information on the general structure, synthesis methods, and biological studies of synthesized NOSartans. In silico evaluation of all NO-Sartans and approved sartans against three key SARS-CoV- -2 targets, namely Mpro (PDB ID: 6LU7), NSP16 (PDB ID: 6WKQ), and ACE-2 (PDB ID: 1R4L), was performed using MOE.

Results: Almost all NO-Sartans and approved sartans demonstrated promising results in inhibiting these SARS-CoV-2 targets. Compound 36 (CLC-1280) showed the best docking scores against the three evaluated targets and was further evaluated using molecular dynamics (MD) simulations.

Conclusion: Based on our in silico studies, CLC-1280 (a Valsartan dinitrate) has the potential to be considered as an inhibitor of the SARS-CoV-2 virus. However, further in vitro and in vivo evaluations are necessary for the drug development process.

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
自引率
0.00%
发文量
0
期刊最新文献
Computational Screening of Novel Nitroimidazole Candidates: Targeting Key Enzymes of Oral Anaerobes for Anti-Parasitic Potential. Preliminary Characterization of the Vasorelaxant Effect of Thymus atlanticus (Ball) Roussine Using Optical Methods. AI in Clinical Trials and Drug Development: Challenges and Potential Advancements. An Update on Clinically Evaluated Medicinal Plants for Psoriasis Management. In Vitro Antibacterial Activity of Adiantum capillus Veneris Extraction with Methanol, Chloroform, and Ether Solvents against Methicillin-resistant Staphylococcus aureus.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1