Potentially Highly Effective Drugs for COVID-19: Virtual Screening and Molecular Docking Study Through PyRx-Vina Approach

Fatemeh Houshmand, Sara Houshmand
{"title":"Potentially Highly Effective Drugs for COVID-19: Virtual Screening and Molecular Docking Study Through PyRx-Vina Approach","authors":"Fatemeh Houshmand, Sara Houshmand","doi":"10.30699/fhi.v12i0.478","DOIUrl":null,"url":null,"abstract":"Introduction: The World Health Organization (WHO) has declared the novel coronavirus (COVID-2019) infection outbreak a global health emergency. Drug repurposing, which concerns the investigation of existing drugs for new therapeutic target indications, has emerged as a successful strategy for drug discovery due to the reduced costs and expedited approval procedures.Material and Methods: The crystal structure of a protein essential for virus replication has been filed in the Protein Data Bank recently. Based on this structure and existing experimental datasets for SARS-CoV2(COVID-19) we present results deriving from the virtual screening of a database of more than 1000 drugs in the DrugBank that have been approved by Food and Drug Administration (FDA).Results: Results showed that some of the known protease inhibitors currently used in HIV and Cancer infections might be helpful for the therapy of COVID-19 also. Results also showed that Levomefolic acid, or vitamin B9, is recommended therapy because of its oral sources and no side effects.Conclusion: Between all studied FDA-approved drug, VitaminB9 and Etoposide which used for HIV protease inhibitor, revealed strong interaction with protease binding pocket and placed well into the pocket even better than the lopinavir-ritonavir, and since this compound is FDA-approved and successfully passed various testing steps, therefor there is a hope that this drug, could be a potential drug to treating the COVID-19.","PeriodicalId":154611,"journal":{"name":"Frontiers in Health Informatics","volume":"19 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Health Informatics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.30699/fhi.v12i0.478","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Introduction: The World Health Organization (WHO) has declared the novel coronavirus (COVID-2019) infection outbreak a global health emergency. Drug repurposing, which concerns the investigation of existing drugs for new therapeutic target indications, has emerged as a successful strategy for drug discovery due to the reduced costs and expedited approval procedures.Material and Methods: The crystal structure of a protein essential for virus replication has been filed in the Protein Data Bank recently. Based on this structure and existing experimental datasets for SARS-CoV2(COVID-19) we present results deriving from the virtual screening of a database of more than 1000 drugs in the DrugBank that have been approved by Food and Drug Administration (FDA).Results: Results showed that some of the known protease inhibitors currently used in HIV and Cancer infections might be helpful for the therapy of COVID-19 also. Results also showed that Levomefolic acid, or vitamin B9, is recommended therapy because of its oral sources and no side effects.Conclusion: Between all studied FDA-approved drug, VitaminB9 and Etoposide which used for HIV protease inhibitor, revealed strong interaction with protease binding pocket and placed well into the pocket even better than the lopinavir-ritonavir, and since this compound is FDA-approved and successfully passed various testing steps, therefor there is a hope that this drug, could be a potential drug to treating the COVID-19.
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
新型冠状病毒潜在高效药物:基于PyRx-Vina方法的虚拟筛选和分子对接研究
导言:世界卫生组织(世卫组织)宣布新型冠状病毒(COVID-2019)感染疫情为全球突发卫生事件。药物再利用涉及对现有药物进行新的治疗目标适应症的调查,由于降低了成本和加快了批准程序,已成为药物发现的一种成功策略。材料和方法:最近,一种病毒复制所必需的蛋白质的晶体结构已在蛋白质数据库中归档。基于这种结构和现有的SARS-CoV2(COVID-19)实验数据集,我们提出了对美国食品和药物管理局(FDA)批准的药物库中1000多种药物的数据库进行虚拟筛选的结果。结果:目前已知的一些用于HIV和癌症感染的蛋白酶抑制剂可能对COVID-19的治疗也有帮助。研究结果还表明,左旋叶酸,或维生素B9,是推荐的治疗方法,因为它的口服来源,没有副作用。结论:在所研究的fda批准的药物中,作为HIV蛋白酶抑制剂的维生素b9和依托泊苷与蛋白酶结合袋的相互作用较强,且比洛匹那韦-利托那韦更易于进入蛋白酶结合袋,且该化合物已获得fda批准并成功通过了各项测试步骤,因此有望成为治疗COVID-19的潜在药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
1.20
自引率
0.00%
发文量
0
期刊最新文献
Self-Care Application for Rheumatoid Arthritis: Identifying Key Data Elements Effective use of electronic health records system for healthcare delivery in Ghana Predictive Modeling of COVID-19 Hospitalization Using Twenty Machine Learning Classification Algorithms on Cohort Data Development and Usability Evaluation of a Web-Based Health Information Technology Dashboard of Quality and Economic Indicators Potentially Highly Effective Drugs for COVID-19: Virtual Screening and Molecular Docking Study Through PyRx-Vina Approach
×
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