{"title":"作为 SAR-CoV-2 潜在多靶点抑制剂的迷迭香酸:一种硅学虚拟筛选方法","authors":"Sumit Kumar, Vikash Kumar","doi":"10.2174/0126667975275509231211062032","DOIUrl":null,"url":null,"abstract":"\n\nRosmarinic acid, a natural compound found in various plants like rosemary\nand lemon balm, may have potential as a multi-targeted inhibitor for SARS-CoV-2, a strain of virus\nresponsible for COVID-19. SARS-CoV-2, a fusion protein of S1 and S2 subunits, has multiple precursors\nangiotensin-converting enzyme2 (ACE2), transmembrane serine protease 2 (TMPRSS2),\npapain-like protease (PLpro), and 3-chymotrypsin-like protease (3CLpro). The chemical interaction\nof Rosmarinic acid with SARS-CoV-2 is of major interest reported here.\n\n\n\nThe quantitative study of Rosmarinic acid with various precursors of SARS-CoV-2 has\nbeen accounted for in detail. Furthermore, the conformational flexibility of Rosmarinic acid has also\nbeen investigated during the interaction with four different precursors of SARS-CoV-2.\n\n\n\nThis investigation delves deeply into the analysis of various aspects, including geometric\nparameters, atomic charge, the energy gap between the highest occupied and lowest unoccupied molecular\norbitals, dipole moments, and the analysis of non-covalent interactions (NCI). Furthermore,\nthe study incorporates molecular docking techniques in conjunction with thorough quantum chemical\ncalculations to provide comprehensive insights.\n\n\n\nRosmarinic acid shows promise as a versatile inhibitor of SARS-CoV-2, the virus responsible\nfor COVID-19. It can target multiple key precursors of the virus, including TMPRSS2, angiotensin-\nconverting enzyme2, 3CLpro, and PLpro, found in the fusion protein comprising S1 and S2 subunits.\nThis study delves into the quantitative analysis of Rosmarinic acid's interactions with these\nprecursors. Its adaptable structure allows it to engage with them effectively. Various molecular parameters,\nincluding atomic charge, energy gap between molecular orbitals, dipole moment, and noncovalent\ninteractions, are comprehensively explored.\n\n\n\nCombining molecular docking and quantum mechanics, the findings suggest Rosmarinic\nacid's potential as a multi-targeted SARS-CoV-2 inhibitor.\n","PeriodicalId":10815,"journal":{"name":"Coronaviruses","volume":" 15","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rosmarinic Acid as a Potential Multi-targeted Inhibitor for SAR-CoV-2:\\nAn In silico Virtual Screening Approach\",\"authors\":\"Sumit Kumar, Vikash Kumar\",\"doi\":\"10.2174/0126667975275509231211062032\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n\\nRosmarinic acid, a natural compound found in various plants like rosemary\\nand lemon balm, may have potential as a multi-targeted inhibitor for SARS-CoV-2, a strain of virus\\nresponsible for COVID-19. SARS-CoV-2, a fusion protein of S1 and S2 subunits, has multiple precursors\\nangiotensin-converting enzyme2 (ACE2), transmembrane serine protease 2 (TMPRSS2),\\npapain-like protease (PLpro), and 3-chymotrypsin-like protease (3CLpro). The chemical interaction\\nof Rosmarinic acid with SARS-CoV-2 is of major interest reported here.\\n\\n\\n\\nThe quantitative study of Rosmarinic acid with various precursors of SARS-CoV-2 has\\nbeen accounted for in detail. Furthermore, the conformational flexibility of Rosmarinic acid has also\\nbeen investigated during the interaction with four different precursors of SARS-CoV-2.\\n\\n\\n\\nThis investigation delves deeply into the analysis of various aspects, including geometric\\nparameters, atomic charge, the energy gap between the highest occupied and lowest unoccupied molecular\\norbitals, dipole moments, and the analysis of non-covalent interactions (NCI). Furthermore,\\nthe study incorporates molecular docking techniques in conjunction with thorough quantum chemical\\ncalculations to provide comprehensive insights.\\n\\n\\n\\nRosmarinic acid shows promise as a versatile inhibitor of SARS-CoV-2, the virus responsible\\nfor COVID-19. It can target multiple key precursors of the virus, including TMPRSS2, angiotensin-\\nconverting enzyme2, 3CLpro, and PLpro, found in the fusion protein comprising S1 and S2 subunits.\\nThis study delves into the quantitative analysis of Rosmarinic acid's interactions with these\\nprecursors. Its adaptable structure allows it to engage with them effectively. Various molecular parameters,\\nincluding atomic charge, energy gap between molecular orbitals, dipole moment, and noncovalent\\ninteractions, are comprehensively explored.\\n\\n\\n\\nCombining molecular docking and quantum mechanics, the findings suggest Rosmarinic\\nacid's potential as a multi-targeted SARS-CoV-2 inhibitor.\\n\",\"PeriodicalId\":10815,\"journal\":{\"name\":\"Coronaviruses\",\"volume\":\" 15\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-12-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Coronaviruses\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2174/0126667975275509231211062032\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Coronaviruses","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/0126667975275509231211062032","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Rosmarinic Acid as a Potential Multi-targeted Inhibitor for SAR-CoV-2:
An In silico Virtual Screening Approach
Rosmarinic acid, a natural compound found in various plants like rosemary
and lemon balm, may have potential as a multi-targeted inhibitor for SARS-CoV-2, a strain of virus
responsible for COVID-19. SARS-CoV-2, a fusion protein of S1 and S2 subunits, has multiple precursors
angiotensin-converting enzyme2 (ACE2), transmembrane serine protease 2 (TMPRSS2),
papain-like protease (PLpro), and 3-chymotrypsin-like protease (3CLpro). The chemical interaction
of Rosmarinic acid with SARS-CoV-2 is of major interest reported here.
The quantitative study of Rosmarinic acid with various precursors of SARS-CoV-2 has
been accounted for in detail. Furthermore, the conformational flexibility of Rosmarinic acid has also
been investigated during the interaction with four different precursors of SARS-CoV-2.
This investigation delves deeply into the analysis of various aspects, including geometric
parameters, atomic charge, the energy gap between the highest occupied and lowest unoccupied molecular
orbitals, dipole moments, and the analysis of non-covalent interactions (NCI). Furthermore,
the study incorporates molecular docking techniques in conjunction with thorough quantum chemical
calculations to provide comprehensive insights.
Rosmarinic acid shows promise as a versatile inhibitor of SARS-CoV-2, the virus responsible
for COVID-19. It can target multiple key precursors of the virus, including TMPRSS2, angiotensin-
converting enzyme2, 3CLpro, and PLpro, found in the fusion protein comprising S1 and S2 subunits.
This study delves into the quantitative analysis of Rosmarinic acid's interactions with these
precursors. Its adaptable structure allows it to engage with them effectively. Various molecular parameters,
including atomic charge, energy gap between molecular orbitals, dipole moment, and noncovalent
interactions, are comprehensively explored.
Combining molecular docking and quantum mechanics, the findings suggest Rosmarinic
acid's potential as a multi-targeted SARS-CoV-2 inhibitor.