Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/10477
Full metadata record
DC FieldValueLanguage
dc.contributor.authorRajpoot, Sajjanen_US
dc.contributor.authorSaqib, Uzmaen_US
dc.contributor.authorBaig, Mirza Saqiben_US
dc.date.accessioned2022-07-15T10:40:20Z-
dc.date.available2022-07-15T10:40:20Z-
dc.date.issued2022-
dc.identifier.citationWang, Y., Rajpoot, S., Li, P., Lavrijsen, M., Ma, Z., Hirani, N., Saqib, U., Pan, Q., & Baig, M. S. (2022). Repurposing dyphylline as a pan-coronavirus antiviral therapy. Future Medicinal Chemistry, 14(10), 685–699. https://doi.org/10.4155/fmc-2021-0311en_US
dc.identifier.issn1756-8919-
dc.identifier.otherEID(2-s2.0-85130562733)-
dc.identifier.urihttps://doi.org/10.4155/fmc-2021-0311-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/10477-
dc.description.abstractBackground: In the last two decades, the world has witnessed the emergence of zoonotic corona viruses (CoVs), which cause mild to severe respiratory diseases in humans. Human coronaviruses (HCoVs), mainly from the alpha-CoV and beta-CoV genera, have evolved to be highly pathogenic, such as SARS-CoV-2 causing the COVID-19 pandemic. These coronaviruses carry functional enzymes necessary for the virus life cycle, which represent attractive antiviral targets. Methods & Results: We aimed to therapeutically target the main protease (Mpro) of HCoV-NL63 and HCoV-229E (from alpha-CoV genus) and HCoV-OC43 and SARS-CoV-2 (from beta-CoV genus). Through virtual screening, we identified an FDA-approved drug dyphylline, a xanthine derivate, that binds to the catalytic dyad residues; histidine and cystine of the Mpro structures. Importantly, dyphylline dose-dependently inhibited the viral replication in cell culture models infected with the viruses. Conclusion: Our findings support the repurposing of dyphylline as a pan-coronavirus antiviral agent. © 2022 Newlands Press.en_US
dc.language.isoenen_US
dc.publisherFuture Medicine Ltd.en_US
dc.sourceFuture Medicinal Chemistryen_US
dc.subjectcoronavirus 3C proteaseen_US
dc.subjectdiprophyllineen_US
dc.subjectantivirus agenten_US
dc.subjectdiprophyllineen_US
dc.subjectanimal cellen_US
dc.subjectArticleen_US
dc.subjectcontrolled studyen_US
dc.subjectcoronavirus disease 2019en_US
dc.subjectdrug repositioningen_US
dc.subjectdrug structureen_US
dc.subjectFood and Drug Administrationen_US
dc.subjecthumanen_US
dc.subjecthuman cellen_US
dc.subjectlife cycleen_US
dc.subjectnonhumanen_US
dc.subjectSARS-CoV-2 Alphaen_US
dc.subjectSARS-CoV-2 Betaen_US
dc.subjectSevere acute respiratory syndrome coronavirus 2en_US
dc.subjectvirus replicationen_US
dc.subjectchemistryen_US
dc.subjectdrug repositioningen_US
dc.subjectdrug therapyen_US
dc.subjectpandemicen_US
dc.subjectAntiviral Agentsen_US
dc.subjectCOVID-19en_US
dc.subjectDrug Repositioningen_US
dc.subjectDyphyllineen_US
dc.subjectHumansen_US
dc.subjectPandemicsen_US
dc.subjectSARS-CoV-2en_US
dc.titleRepurposing dyphylline as a pan-coronavirus antiviral therapyen_US
dc.typeJournal Articleen_US
dc.rights.licenseAll Open Access, Hybrid Gold, Green-
Appears in Collections:Department of Biosciences and Biomedical Engineering

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Altmetric Badge: