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Structure-guided design and photochemical synthesis of new carbamo(dithioperoxo)thioates with improved potencies to SARS-CoV-2 3CL pro .
- Source :
-
Bioorganic & medicinal chemistry [Bioorg Med Chem] 2024 Nov 15; Vol. 114, pp. 117940. Date of Electronic Publication: 2024 Oct 11. - Publication Year :
- 2024
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Abstract
- The COVID-19 pandemic, caused by the SARS-CoV-2 virus, has triggered a protracted global pandemic from 2019 to 2022, and posed a significant threat to human health. One of the non-structural proteins 3CL <superscript>pro</superscript> of SARS-CoV-2 is considered as a validated target for the development of inhibitors against the virus. Disulfiram has been reported as a covalent inhibitor of 3CL <superscript>pro</superscript> ; however, its structure lacks bonding site with active pockets of 3CL <superscript>pro</superscript> and its highly symmetric structure doesn't match well with the irregular cavity of the active center, limiting its therapeutic applications. To enhance their affinity for the 3CL <superscript>pro</superscript> target, in this study, two kinds of disulfiram derivatives, designed based on the reevaluation and optimization of disulfiram, have been synthesized through photoredox chemistry, and the novel carbamo(dithioperoxo)thioates 4g-m were found to display 5-17 folds potency against SARS-CoV-2 3CL <superscript>pro</superscript> compared to the parent disulfiram, with resulting half-maximal inhibitory concentration (IC <subscript>50</subscript> ) values ranging from 0.14-0.47 μM. Carbamo(dithioperoxo)thioates 4i containing a 4-hydroxy piperidine and a 4-trifluoromethyl phenyl ring, was identified as the most potent inhibitor to both 3CL <superscript>pro</superscript> (IC <subscript>50</subscript>  = 0.14 μM) and PL <superscript>pro</superscript> (IC <subscript>50</subscript>  = 0.04 μM). Furthermore, molecular dynamics simulations, binding free energy analysis and mass analysis were performed and provided insights on the stability, conformational behavior, and interactions of 4g with 3CL <superscript>pro</superscript> . The green synthetic methodology, the privileged carbamo(dithioperoxo)thioate scaffold, and the molecular mechanisms presented might serve as a useful system for the further discovery of highly potent inhibitors targeting SARS-CoV-2 3CL <superscript>pro</superscript> .<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier Ltd. All rights reserved.)
- Subjects :
- Humans
COVID-19 virology
COVID-19 Drug Treatment
Disulfiram pharmacology
Disulfiram chemical synthesis
Disulfiram chemistry
Molecular Docking Simulation
Molecular Structure
Photochemical Processes
Structure-Activity Relationship
Sulfhydryl Compounds chemistry
Sulfhydryl Compounds pharmacology
Piperidines chemistry
Piperidines pharmacology
Antiviral Agents pharmacology
Antiviral Agents chemical synthesis
Antiviral Agents chemistry
Coronavirus 3C Proteases antagonists & inhibitors
Coronavirus 3C Proteases metabolism
Coronavirus 3C Proteases chemistry
Drug Design
SARS-CoV-2 drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1464-3391
- Volume :
- 114
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 39442491
- Full Text :
- https://doi.org/10.1016/j.bmc.2024.117940