Screening of the antileishmanial and antiplasmodial potential of synthetic 2-arylquinoline analogs

ABSTRACT: In this study, six analogs of 2-arylquinoline were synthesized and evaluated for their in vitro and in vivo antiplasmodial and leishmanicidal activity. At a later stage, hemolytic activity and druggability were tested in vitro and in silico, respectively, observing as a result: firstly, co...

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Autores:
Robledo Restrepo, Sara María
Espinosa Sáez, Roger
Pineda, Tatiana
Murillo, Javier
Zúñiga, César
Yañez, Osvaldo
Cantero López, Plinio
Sáez Vega, Alex
Guzmán Teran, Camilo
Tipo de recurso:
Article of investigation
Fecha de publicación:
2023
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/43580
Acceso en línea:
https://hdl.handle.net/10495/43580
Palabra clave:
Antimaláricos
Antimalarials
Antiprotozoarios
Antiprotozoal Agents
Leishmania
Simulación del Acoplamiento Molecular
Molecular Docking Simulation
Relación Estructura-Actividad
Structure-Activity Relationship
https://id.nlm.nih.gov/mesh/D000962
https://id.nlm.nih.gov/mesh/D000981
https://id.nlm.nih.gov/mesh/D007891
https://id.nlm.nih.gov/mesh/D062105
https://id.nlm.nih.gov/mesh/D013329
Rights
openAccess
License
https://creativecommons.org/licenses/by/4.0/
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network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv Screening of the antileishmanial and antiplasmodial potential of synthetic 2-arylquinoline analogs
title Screening of the antileishmanial and antiplasmodial potential of synthetic 2-arylquinoline analogs
spellingShingle Screening of the antileishmanial and antiplasmodial potential of synthetic 2-arylquinoline analogs
Antimaláricos
Antimalarials
Antiprotozoarios
Antiprotozoal Agents
Leishmania
Simulación del Acoplamiento Molecular
Molecular Docking Simulation
Relación Estructura-Actividad
Structure-Activity Relationship
https://id.nlm.nih.gov/mesh/D000962
https://id.nlm.nih.gov/mesh/D000981
https://id.nlm.nih.gov/mesh/D007891
https://id.nlm.nih.gov/mesh/D062105
https://id.nlm.nih.gov/mesh/D013329
title_short Screening of the antileishmanial and antiplasmodial potential of synthetic 2-arylquinoline analogs
title_full Screening of the antileishmanial and antiplasmodial potential of synthetic 2-arylquinoline analogs
title_fullStr Screening of the antileishmanial and antiplasmodial potential of synthetic 2-arylquinoline analogs
title_full_unstemmed Screening of the antileishmanial and antiplasmodial potential of synthetic 2-arylquinoline analogs
title_sort Screening of the antileishmanial and antiplasmodial potential of synthetic 2-arylquinoline analogs
dc.creator.fl_str_mv Robledo Restrepo, Sara María
Espinosa Sáez, Roger
Pineda, Tatiana
Murillo, Javier
Zúñiga, César
Yañez, Osvaldo
Cantero López, Plinio
Sáez Vega, Alex
Guzmán Teran, Camilo
dc.contributor.author.none.fl_str_mv Robledo Restrepo, Sara María
Espinosa Sáez, Roger
Pineda, Tatiana
Murillo, Javier
Zúñiga, César
Yañez, Osvaldo
Cantero López, Plinio
Sáez Vega, Alex
Guzmán Teran, Camilo
dc.contributor.researchgroup.spa.fl_str_mv Programa de Estudio y Control de Enfermedades Tropicales (PECET)
dc.subject.decs.none.fl_str_mv Antimaláricos
Antimalarials
Antiprotozoarios
Antiprotozoal Agents
Leishmania
Simulación del Acoplamiento Molecular
Molecular Docking Simulation
Relación Estructura-Actividad
Structure-Activity Relationship
topic Antimaláricos
Antimalarials
Antiprotozoarios
Antiprotozoal Agents
Leishmania
Simulación del Acoplamiento Molecular
Molecular Docking Simulation
Relación Estructura-Actividad
Structure-Activity Relationship
https://id.nlm.nih.gov/mesh/D000962
https://id.nlm.nih.gov/mesh/D000981
https://id.nlm.nih.gov/mesh/D007891
https://id.nlm.nih.gov/mesh/D062105
https://id.nlm.nih.gov/mesh/D013329
dc.subject.meshuri.none.fl_str_mv https://id.nlm.nih.gov/mesh/D000962
https://id.nlm.nih.gov/mesh/D000981
https://id.nlm.nih.gov/mesh/D007891
https://id.nlm.nih.gov/mesh/D062105
https://id.nlm.nih.gov/mesh/D013329
description ABSTRACT: In this study, six analogs of 2-arylquinoline were synthesized and evaluated for their in vitro and in vivo antiplasmodial and leishmanicidal activity. At a later stage, hemolytic activity and druggability were tested in vitro and in silico, respectively, observing as a result: firstly, compounds showed half-maximal effective concentration (EC50) values between 3.6 and 19.3 µM. Likewise, a treatment using the compounds 4a-f caused improvement in most of the treated hamsters and cured some of them. Regarding the antiplasmodial activity, the compounds showed moderate to high activity, although they did not show hemolytic activity. Furthermore, 4e and 4f compounds were not able to control P. berghei infection when administered to animal models. Molecular dynamic simulations, molecular docking and ligand binding affinity indicate good characteristics of the studied compounds, which are expected to be active. And lastly, the compounds are absorbable at the hematoencephalic barrier but not in the gastrointestinal tract. In summary, ADMET properties suggest that these molecules may be used as a safe treatment against Leishmania.
publishDate 2023
dc.date.issued.none.fl_str_mv 2023
dc.date.accessioned.none.fl_str_mv 2024-11-19T00:01:53Z
dc.date.available.none.fl_str_mv 2024-11-19T00:01:53Z
dc.type.spa.fl_str_mv Artículo de investigación
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dc.identifier.citation.spa.fl_str_mv Espinosa-Saez R, Robledo SM, Pineda T, Murillo J, Zúñiga C, Yañez O, Cantero-López P, Saez-Vega A, Guzmán-Teran C. Screening of the antileishmanial and antiplasmodial potential of synthetic 2-arylquinoline analogs. Sci Rep. 2023 Oct 16;13(1):17523. doi: 10.1038/s41598-023-43805-4.
dc.identifier.issn.none.fl_str_mv 2045-2322
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/43580
dc.identifier.doi.none.fl_str_mv 10.1038/s41598-023-43805-4
identifier_str_mv Espinosa-Saez R, Robledo SM, Pineda T, Murillo J, Zúñiga C, Yañez O, Cantero-López P, Saez-Vega A, Guzmán-Teran C. Screening of the antileishmanial and antiplasmodial potential of synthetic 2-arylquinoline analogs. Sci Rep. 2023 Oct 16;13(1):17523. doi: 10.1038/s41598-023-43805-4.
2045-2322
10.1038/s41598-023-43805-4
url https://hdl.handle.net/10495/43580
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Sci. Rep.
dc.relation.citationendpage.spa.fl_str_mv 16
dc.relation.citationissue.spa.fl_str_mv 1
dc.relation.citationstartpage.spa.fl_str_mv 1
dc.relation.citationvolume.spa.fl_str_mv 13
dc.relation.ispartofjournal.spa.fl_str_mv Scientific Reports
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institution Universidad de Antioquia
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spelling Robledo Restrepo, Sara MaríaEspinosa Sáez, RogerPineda, TatianaMurillo, JavierZúñiga, CésarYañez, OsvaldoCantero López, PlinioSáez Vega, AlexGuzmán Teran, CamiloPrograma de Estudio y Control de Enfermedades Tropicales (PECET)2024-11-19T00:01:53Z2024-11-19T00:01:53Z2023Espinosa-Saez R, Robledo SM, Pineda T, Murillo J, Zúñiga C, Yañez O, Cantero-López P, Saez-Vega A, Guzmán-Teran C. Screening of the antileishmanial and antiplasmodial potential of synthetic 2-arylquinoline analogs. Sci Rep. 2023 Oct 16;13(1):17523. doi: 10.1038/s41598-023-43805-4.2045-2322https://hdl.handle.net/10495/4358010.1038/s41598-023-43805-4ABSTRACT: In this study, six analogs of 2-arylquinoline were synthesized and evaluated for their in vitro and in vivo antiplasmodial and leishmanicidal activity. At a later stage, hemolytic activity and druggability were tested in vitro and in silico, respectively, observing as a result: firstly, compounds showed half-maximal effective concentration (EC50) values between 3.6 and 19.3 µM. Likewise, a treatment using the compounds 4a-f caused improvement in most of the treated hamsters and cured some of them. Regarding the antiplasmodial activity, the compounds showed moderate to high activity, although they did not show hemolytic activity. Furthermore, 4e and 4f compounds were not able to control P. berghei infection when administered to animal models. Molecular dynamic simulations, molecular docking and ligand binding affinity indicate good characteristics of the studied compounds, which are expected to be active. And lastly, the compounds are absorbable at the hematoencephalic barrier but not in the gastrointestinal tract. In summary, ADMET properties suggest that these molecules may be used as a safe treatment against Leishmania.Universidad de AntioquiaUniversidad de CórdobaUniversidad Andrés BelloCOL001509916 páginasapplication/pdfengNature Publishing GroupLondres, Inglaterrahttps://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/2.5/co/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Screening of the antileishmanial and antiplasmodial potential of synthetic 2-arylquinoline analogsArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionAntimaláricosAntimalarialsAntiprotozoariosAntiprotozoal AgentsLeishmaniaSimulación del Acoplamiento MolecularMolecular Docking SimulationRelación Estructura-ActividadStructure-Activity Relationshiphttps://id.nlm.nih.gov/mesh/D000962https://id.nlm.nih.gov/mesh/D000981https://id.nlm.nih.gov/mesh/D007891https://id.nlm.nih.gov/mesh/D062105https://id.nlm.nih.gov/mesh/D013329Sci. 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