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Is PF-00835231 a Pan-SARS-CoV-2 Mpro Inhibitor? A Comparative Study

DC Field Value Language
dc.contributor.author동재준-
dc.date.accessioned2021-09-29T00:44:34Z-
dc.date.available2021-09-29T00:44:34Z-
dc.date.issued2021-03-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/184013-
dc.description.abstractThe COVID-19 outbreak continues to spread worldwide at a rapid rate. Currently, the absence of any effective antiviral treatment is the major concern for the global population. The reports of the occurrence of various point mutations within the important therapeutic target protein of SARS-CoV-2 has elevated the problem. The SARS-CoV-2 main protease (Mpro) is a major therapeutic target for new antiviral designs. In this study, the efficacy of PF-00835231 was investigated (a Mpro inhibitor under clinical trials) against the Mpro and their reported mutants. Various in silico approaches were used to investigate and compare the efficacy of PF-00835231 and five drugs previously documented to inhibit the Mpro. Our study shows that PF-00835231 is not only effective against the wild type but demonstrates a high affinity against the studied mutants as well.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherMDPI-
dc.relation.isPartOfMOLECULES-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAntiviral Agents / chemistry*-
dc.subject.MESHAntiviral Agents / pharmacology*-
dc.subject.MESHBinding Sites-
dc.subject.MESHCOVID-19 / drug therapy-
dc.subject.MESHComputer Simulation-
dc.subject.MESHCoronavirus 3C Proteases / antagonists & inhibitors*-
dc.subject.MESHCoronavirus 3C Proteases / chemistry-
dc.subject.MESHCoronavirus 3C Proteases / genetics-
dc.subject.MESHDatabases, Protein-
dc.subject.MESHDiarylquinolines / chemistry-
dc.subject.MESHDiarylquinolines / pharmacology-
dc.subject.MESHDihydropyridines / chemistry-
dc.subject.MESHDihydropyridines / pharmacology-
dc.subject.MESHHumans-
dc.subject.MESHIndoles / chemistry*-
dc.subject.MESHIndoles / pharmacology*-
dc.subject.MESHLeucine / chemistry*-
dc.subject.MESHLeucine / pharmacology*-
dc.subject.MESHLigands-
dc.subject.MESHMolecular Docking Simulation-
dc.subject.MESHMolecular Dynamics Simulation-
dc.subject.MESHNitrobenzenes / chemistry-
dc.subject.MESHNitrobenzenes / pharmacology-
dc.subject.MESHNitrophenols / chemistry-
dc.subject.MESHNitrophenols / pharmacology-
dc.subject.MESHOrganophosphorus Compounds / chemistry-
dc.subject.MESHOrganophosphorus Compounds / pharmacology-
dc.subject.MESHPiperazines / chemistry-
dc.subject.MESHPiperazines / pharmacology-
dc.subject.MESHProline / analogs & derivatives-
dc.subject.MESHProline / chemistry-
dc.subject.MESHProline / pharmacology-
dc.subject.MESHProtease Inhibitors / chemistry*-
dc.subject.MESHProtease Inhibitors / pharmacology*-
dc.subject.MESHPyrrolidinones / chemistry*-
dc.subject.MESHPyrrolidinones / pharmacology*-
dc.subject.MESHSARS-CoV-2 / drug effects-
dc.subject.MESHSARS-CoV-2 / genetics-
dc.titleIs PF-00835231 a Pan-SARS-CoV-2 Mpro Inhibitor? A Comparative Study-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Family Medicine (가정의학교실)-
dc.contributor.googleauthorMohammad Hassan Baig-
dc.contributor.googleauthorTanuj Sharma-
dc.contributor.googleauthorIrfan Ahmad-
dc.contributor.googleauthorMohammed Abohashrh-
dc.contributor.googleauthorMohammad Mahtab Alam-
dc.contributor.googleauthorJae-June Dong-
dc.identifier.doi10.3390/molecules26061678-
dc.contributor.localIdA04927-
dc.relation.journalcodeJ03201-
dc.identifier.eissn1420-3049-
dc.identifier.pmid33802860-
dc.subject.keywordPF-00835231-
dc.subject.keywordSARS-CoV-2-
dc.subject.keywordinhibitors-
dc.subject.keywordmain protease-
dc.subject.keywordmutants-
dc.contributor.alternativeNameDong, Jae June-
dc.contributor.affiliatedAuthor동재준-
dc.citation.volume26-
dc.citation.number6-
dc.citation.startPage1678-
dc.identifier.bibliographicCitationMOLECULES, Vol.26(6) : 1678, 2021-03-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Family Medicine (가정의학교실) > 1. Journal Papers

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