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...
- 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/
| id |
UDEA2_69366030867ff0552d416f23748a624f |
|---|---|
| oai_identifier_str |
oai:bibliotecadigital.udea.edu.co:10495/43580 |
| network_acronym_str |
UDEA2 |
| 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 |
| dc.type.coar.spa.fl_str_mv |
http://purl.org/coar/resource_type/c_2df8fbb1 |
| dc.type.redcol.spa.fl_str_mv |
https://purl.org/redcol/resource_type/ART |
| dc.type.coarversion.spa.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
| dc.type.driver.spa.fl_str_mv |
info:eu-repo/semantics/article |
| dc.type.version.spa.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
| format |
http://purl.org/coar/resource_type/c_2df8fbb1 |
| status_str |
publishedVersion |
| 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 |
| dc.rights.uri.spa.fl_str_mv |
https://creativecommons.org/licenses/by/4.0/ |
| dc.rights.uri.*.fl_str_mv |
http://creativecommons.org/licenses/by/2.5/co/ |
| dc.rights.accessrights.spa.fl_str_mv |
info:eu-repo/semantics/openAccess |
| dc.rights.coar.spa.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
| rights_invalid_str_mv |
https://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/2.5/co/ http://purl.org/coar/access_right/c_abf2 |
| eu_rights_str_mv |
openAccess |
| dc.format.extent.spa.fl_str_mv |
16 páginas |
| dc.format.mimetype.spa.fl_str_mv |
application/pdf |
| dc.publisher.spa.fl_str_mv |
Nature Publishing Group |
| dc.publisher.place.spa.fl_str_mv |
Londres, Inglaterra |
| institution |
Universidad de Antioquia |
| bitstream.url.fl_str_mv |
https://bibliotecadigital.udea.edu.co/bitstreams/90e94d6a-790c-4cff-a42b-fa2ab933c84c/download https://bibliotecadigital.udea.edu.co/bitstreams/2d853f26-f658-4be9-bbeb-9697ea5e6dbf/download https://bibliotecadigital.udea.edu.co/bitstreams/c22266cc-62bb-4e9d-a5d9-9960856bf7b7/download https://bibliotecadigital.udea.edu.co/bitstreams/c4ae9b23-6e4f-46f3-ac39-2bd633e504ce/download https://bibliotecadigital.udea.edu.co/bitstreams/4317ba8e-7a9f-407e-b1df-a30813058518/download |
| bitstream.checksum.fl_str_mv |
1646d1f6b96dbbbc38035efc9239ac9c 2dc726958636e7cb84078092363767e4 8a4605be74aa9ea9d79846c1fba20a33 044a87c602ae2e479eed1b31dad894fa 3b845f1b1112175eed916b896716d804 |
| bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 MD5 MD5 MD5 |
| repository.name.fl_str_mv |
Repositorio Institucional de la Universidad de Antioquia |
| repository.mail.fl_str_mv |
aplicacionbibliotecadigitalbiblioteca@udea.edu.co |
| _version_ |
1851052257056915456 |
| 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. Rep.161113Scientific ReportsRoR:03bp5hc83RoR:04nmbd607RoR:01qq57711PublicationCC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8927https://bibliotecadigital.udea.edu.co/bitstreams/90e94d6a-790c-4cff-a42b-fa2ab933c84c/download1646d1f6b96dbbbc38035efc9239ac9cMD52falseAnonymousREADORIGINALRobledoSara_2023_ParasiteCellsInfection.pdfRobledoSara_2023_ParasiteCellsInfection.pdfArtículo de investigaciónapplication/pdf1491361https://bibliotecadigital.udea.edu.co/bitstreams/2d853f26-f658-4be9-bbeb-9697ea5e6dbf/download2dc726958636e7cb84078092363767e4MD51trueAnonymousREADLICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://bibliotecadigital.udea.edu.co/bitstreams/c22266cc-62bb-4e9d-a5d9-9960856bf7b7/download8a4605be74aa9ea9d79846c1fba20a33MD53falseAnonymousREADTEXTRobledoSara_2023_ParasiteCellsInfection.pdf.txtRobledoSara_2023_ParasiteCellsInfection.pdf.txtExtracted texttext/plain94748https://bibliotecadigital.udea.edu.co/bitstreams/c4ae9b23-6e4f-46f3-ac39-2bd633e504ce/download044a87c602ae2e479eed1b31dad894faMD54falseAnonymousREADTHUMBNAILRobledoSara_2023_ParasiteCellsInfection.pdf.jpgRobledoSara_2023_ParasiteCellsInfection.pdf.jpgGenerated Thumbnailimage/jpeg16702https://bibliotecadigital.udea.edu.co/bitstreams/4317ba8e-7a9f-407e-b1df-a30813058518/download3b845f1b1112175eed916b896716d804MD55falseAnonymousREAD10495/43580oai:bibliotecadigital.udea.edu.co:10495/435802025-03-26 19:27:46.484https://creativecommons.org/licenses/by/4.0/open.accesshttps://bibliotecadigital.udea.edu.coRepositorio Institucional de la Universidad de Antioquiaaplicacionbibliotecadigitalbiblioteca@udea.edu.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 |
