Derivatization and combination therapy of current COVID-19 therapeutic agents: a review of mechanistic pathways, adverse effects, and binding sites
| dc.creator | El Kantar, Sally | |
| dc.creator | Nehmeh, Bilal | |
| dc.creator | Saad, Philippe | |
| dc.creator | Mitri, Gabie | |
| dc.creator | Estephan, Celine | |
| dc.creator | Mroueh, Mohamad | |
| dc.creator | Akoury, Elias | |
| dc.creator | Taleb, Robin I. | |
| dc.date.accessioned | 2020-09-01T14:21:51Z | |
| dc.date.available | 2020-09-01T14:21:51Z | |
| dc.date.created | 2020 | |
| dc.description.abstract | Current treatment of patients with coronavirus 2019 (COVID-19) involves repurposed drugs that inhibit viral infection by either binding to their respective targets or via modulating cellular signal transduction. However, there is still a great deal of efficacy enhancement through combination therapy and derivatization. Combination therapy should involve agents with significant activity and different mechanisms of action. The structural map of the interaction between a drug and its target protein will help guide drug discovery for devising safe and effective ways to treat COVID-19. Herein, we report numerous synthetic designs based on enhanced affinity to the viral carbohydrate-rich protein spikes and proteinbinding sites of COVID-19. | spa |
| dc.format.extent | 23 páginas | spa |
| dc.format.mimetype | image/jepg | spa |
| dc.identifier.doi | https://doi.org/10.1016/j.drudis.2020.08.002 | spa |
| dc.identifier.issn | 1359-6446 | spa |
| dc.identifier.other | https://doi.org/10.1016/j.drudis.2020.08.002 | spa |
| dc.identifier.uri | https://hdl.handle.net/20.500.12010/12533 | |
| dc.language.iso | eng | spa |
| dc.publisher | Drug Discovery Today | spa |
| dc.rights.accessrights | info:eu-repo/semantics/embargoedAccess | spa |
| dc.rights.local | Acceso restringido | spa |
| dc.source | reponame:Expeditio Repositorio Institucional UJTL | spa |
| dc.source | instname:Universidad de Bogotá Jorge Tadeo Lozano | spa |
| dc.subject | COVID-19 | spa |
| dc.subject | Remdesivir | spa |
| dc.subject | Hydroxychloroquine | spa |
| dc.subject | Chloroquine | spa |
| dc.subject | Favipiravir | spa |
| dc.subject | Ribavirin | spa |
| dc.subject | Umifenovir | spa |
| dc.subject | Lopinavir | spa |
| dc.subject | Ritonavir | spa |
| dc.subject | Tocilizumab | spa |
| dc.subject | Sarilumab | spa |
| dc.subject | Camostat | spa |
| dc.subject.lemb | Síndrome respiratorio agudo grave | spa |
| dc.subject.lemb | COVID-19 | spa |
| dc.subject.lemb | SARS-CoV-2 | spa |
| dc.subject.lemb | Coronavirus | spa |
| dc.title | Derivatization and combination therapy of current COVID-19 therapeutic agents: a review of mechanistic pathways, adverse effects, and binding sites | spa |
| dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | spa |
| dc.type.hasversion | info:eu-repo/semantics/acceptedVersion | spa |
| dc.type.local | Artículo | spa |
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