Author | dc.contributor.author | Yáñez Osses, Osvaldo Andrés | |
Author | dc.contributor.author | Osorio, Manuel Isaías | |
Author | dc.contributor.author | Areche Medina, Carlos Alberto | |
Author | dc.contributor.author | Vásquez Espinal, Alejandro | |
Author | dc.contributor.author | Bravo, Jéssica | |
Author | dc.contributor.author | Sandoval Aldana, Angélica | |
Author | dc.contributor.author | Pérez Donoso, José M. | |
Author | dc.contributor.author | González Nilo, Fernando Danilo | |
Author | dc.contributor.author | Matos, María Joao | |
Author | dc.contributor.author | Osorio, Edison | |
Author | dc.contributor.author | García Beltrán, Olimpo José | |
Author | dc.contributor.author | Tiznado Vásquez, William Artemio | |
Admission date | dc.date.accessioned | 2022-03-04T18:29:25Z | |
Available date | dc.date.available | 2022-03-04T18:29:25Z | |
Publication date | dc.date.issued | 2021 | |
Cita de ítem | dc.identifier.citation | Biomedicine & Pharmacotherapy 140 (2021) 111764 | es_ES |
Identifier | dc.identifier.other | 10.1016/j.biopha.2021.111764 | |
Identifier | dc.identifier.uri | https://repositorio.uchile.cl/handle/2250/184060 | |
Abstract | dc.description.abstract | Cocoa beans contain antioxidant molecules with the potential to inhibit type 2 coronavirus (SARS-CoV-2), which causes a severe acute respiratory syndrome (COVID-19). In particular, protease. Therefore, using in silico tests, 30 molecules obtained from cocoa were evaluated. Using molecular docking and quantum mechanics calculations, the chemical properties and binding efficiency of each ligand was evaluated, which allowed the selection of 5 compounds of this series. The ability of amentoflavone, isorhoifolin, nicotiflorin, naringin and rutin to bind to the main viral protease was studied by means of free energy calculations and structural analysis performed from molecular dynamics simulations of the enzyme/inhibitor complex. Isorhoifolin and rutin stand out, presenting a more negative binding Delta G than the reference inhibitor N-[(5-methylisoxazol-3-yl)carbonyl]alanyl-L-valylN-1--((1R,2Z)- 4-(benzyloxy)- 4-oxo-1-{[(3R)- 2-oxopyrrolidin-3-yl]methyl}but-2-enyl)-L-leucinamide (N3). These results are consistent with high affinities of these molecules for the major SARS-CoV-2. The results presented in this paper are a solid starting point for future in vitro and in vivo experiments aiming to validate these molecules and /or test similar substances as inhibitors of SARS-CoV-2 protease. | es_ES |
Patrocinador | dc.description.sponsorship | Ministry of Energy, Science, Technology, Environment and Climate Change (MESTECC), Malaysia
Ministry of Education
Ministry of Industry, Commerce and Tourism
Francisco Jose de Caldas Fund RC-FP44842-212-2018
FONTAGRO ATN-RF 16109 RG
Portuguese Foundation for Science and Technology CEECIND/02423/2018
UIDB/00081/2020
National Agency for Research and Development ECOS170045
Comision Nacional de Investigacion Cientifica y Tecnologica (CONICYT)
CONICYT FONDECYT 1211128
ANID/PIA (Chile) ACT192144 | es_ES |
Lenguage | dc.language.iso | en | es_ES |
Publisher | dc.publisher | Elsevier | es_ES |
Type of license | dc.rights | Attribution-NonCommercial-NoDerivs 3.0 United States | * |
Link to License | dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/us/ | * |
Source | dc.source | Biomedicine & Pharmacotherapy | es_ES |
Keywords | dc.subject | Theobroma cacao | es_ES |
Keywords | dc.subject | Antioxidant | es_ES |
Keywords | dc.subject | Bioflavonoids | es_ES |
Keywords | dc.subject | SARS-CoV-2 | es_ES |
Keywords | dc.subject | Molecular dynamics | es_ES |
Keywords | dc.subject | DFT | es_ES |
Título | dc.title | Theobroma cacao L. compounds: Theoretical study and molecular modeling as inhibitors of main SARS-CoV-2 protease | es_ES |
Document type | dc.type | Artículo de revista | es_ES |
dc.description.version | dc.description.version | Versión publicada - versión final del editor | es_ES |
dcterms.accessRights | dcterms.accessRights | Acceso abierto | es_ES |
Cataloguer | uchile.catalogador | cfr | es_ES |
Indexation | uchile.index | Artículo de publícación WoS | es_ES |
Indexation | uchile.index | Artículo de publicación SCOPUS | es_ES |