Exploring the scope of new arylamino alcohol derivatives: Synthesis, antimalarial evaluation, toxicological studies, and target exploration
ABSTRACT: Synthesis of new 1-aryl-3-substituted propanol derivatives followed by structure-activity relationship, in silico drug-likeness, cytotoxicity, genotoxicity, in silico metabolism, in silico pharmacophore modeling, and in vivo studies led to the identification of compounds 22 and 23 with sig...
- Autores:
-
Pabón Vidal, Adriana Lucía
Quiliano, Miguel
Mendoza, Adela
Fong, Kim
Goldfarb, Nathan
Fabing, Isabelle
Vettorazzi, Ariane
López de Cerain, Adela
Dunn, Ben
Garavito, Giovanny
Wright, David
DeHaro, Eric
Pérez Silanes, Silvia
Aldana, Ignacio
Galiano, Silvia
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2016
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/32004
- Acceso en línea:
- https://hdl.handle.net/10495/32004
- Palabra clave:
- Drug-Related Side Effects and Adverse Reactions
Antimaláricos
Antimalarials
Amino Alcoholes
Amino Alcohols
Modelos Animales de Enfermedad
Disease Models, Animal
Concentración 50 Inhibidora
Inhibitory Concentration 50
Malaria Falciparum
Malaria, Falciparum
Plasmodium falciparum
Relación Estructura-Actividad
Structure-Activity Relationship
Resultado del Tratamiento
Treatment Outcome
Análisis de Supervivencia
Survival Analysis
Ratones
Mice
http://id.nlm.nih.gov/mesh/D064420
- Rights
- openAccess
- License
- http://creativecommons.org/licenses/by-nc-nd/2.5/co/
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|
dc.title.spa.fl_str_mv |
Exploring the scope of new arylamino alcohol derivatives: Synthesis, antimalarial evaluation, toxicological studies, and target exploration |
title |
Exploring the scope of new arylamino alcohol derivatives: Synthesis, antimalarial evaluation, toxicological studies, and target exploration |
spellingShingle |
Exploring the scope of new arylamino alcohol derivatives: Synthesis, antimalarial evaluation, toxicological studies, and target exploration Drug-Related Side Effects and Adverse Reactions Antimaláricos Antimalarials Amino Alcoholes Amino Alcohols Modelos Animales de Enfermedad Disease Models, Animal Concentración 50 Inhibidora Inhibitory Concentration 50 Malaria Falciparum Malaria, Falciparum Plasmodium falciparum Relación Estructura-Actividad Structure-Activity Relationship Resultado del Tratamiento Treatment Outcome Análisis de Supervivencia Survival Analysis Ratones Mice http://id.nlm.nih.gov/mesh/D064420 |
title_short |
Exploring the scope of new arylamino alcohol derivatives: Synthesis, antimalarial evaluation, toxicological studies, and target exploration |
title_full |
Exploring the scope of new arylamino alcohol derivatives: Synthesis, antimalarial evaluation, toxicological studies, and target exploration |
title_fullStr |
Exploring the scope of new arylamino alcohol derivatives: Synthesis, antimalarial evaluation, toxicological studies, and target exploration |
title_full_unstemmed |
Exploring the scope of new arylamino alcohol derivatives: Synthesis, antimalarial evaluation, toxicological studies, and target exploration |
title_sort |
Exploring the scope of new arylamino alcohol derivatives: Synthesis, antimalarial evaluation, toxicological studies, and target exploration |
dc.creator.fl_str_mv |
Pabón Vidal, Adriana Lucía Quiliano, Miguel Mendoza, Adela Fong, Kim Goldfarb, Nathan Fabing, Isabelle Vettorazzi, Ariane López de Cerain, Adela Dunn, Ben Garavito, Giovanny Wright, David DeHaro, Eric Pérez Silanes, Silvia Aldana, Ignacio Galiano, Silvia |
dc.contributor.author.none.fl_str_mv |
Pabón Vidal, Adriana Lucía Quiliano, Miguel Mendoza, Adela Fong, Kim Goldfarb, Nathan Fabing, Isabelle Vettorazzi, Ariane López de Cerain, Adela Dunn, Ben Garavito, Giovanny Wright, David DeHaro, Eric Pérez Silanes, Silvia Aldana, Ignacio Galiano, Silvia |
dc.subject.mesh.none.fl_str_mv |
Drug-Related Side Effects and Adverse Reactions |
topic |
Drug-Related Side Effects and Adverse Reactions Antimaláricos Antimalarials Amino Alcoholes Amino Alcohols Modelos Animales de Enfermedad Disease Models, Animal Concentración 50 Inhibidora Inhibitory Concentration 50 Malaria Falciparum Malaria, Falciparum Plasmodium falciparum Relación Estructura-Actividad Structure-Activity Relationship Resultado del Tratamiento Treatment Outcome Análisis de Supervivencia Survival Analysis Ratones Mice http://id.nlm.nih.gov/mesh/D064420 |
dc.subject.decs.none.fl_str_mv |
Antimaláricos Antimalarials Amino Alcoholes Amino Alcohols Modelos Animales de Enfermedad Disease Models, Animal Concentración 50 Inhibidora Inhibitory Concentration 50 Malaria Falciparum Malaria, Falciparum Plasmodium falciparum Relación Estructura-Actividad Structure-Activity Relationship Resultado del Tratamiento Treatment Outcome Análisis de Supervivencia Survival Analysis Ratones Mice |
dc.subject.meshuri.none.fl_str_mv |
http://id.nlm.nih.gov/mesh/D064420 |
description |
ABSTRACT: Synthesis of new 1-aryl-3-substituted propanol derivatives followed by structure-activity relationship, in silico drug-likeness, cytotoxicity, genotoxicity, in silico metabolism, in silico pharmacophore modeling, and in vivo studies led to the identification of compounds 22 and 23 with significant in vitro antiplasmodial activity against drug sensitive (D6 IC50 ≤ 0.19 μM) and multidrug resistant (FCR-3 IC50 ≤ 0.40 μM and C235 IC50 ≤ 0.28 μM) strains of Plasmodium falciparum. Adequate selectivity index and absence of genotoxicity was also observed. Notably, compound 22 displays excellent parasitemia reduction (98 ± 1%), and complete cure with all treated mice surviving through the entire period with no signs of toxicity. One important factor is the agreement between in vitro potency and in vivo studies. Target exploration was performed; this chemotype series exhibits an alternative antimalarial mechanism. |
publishDate |
2016 |
dc.date.issued.none.fl_str_mv |
2016 |
dc.date.accessioned.none.fl_str_mv |
2022-11-13T16:01:20Z |
dc.date.available.none.fl_str_mv |
2022-11-13T16:01:20Z |
dc.type.spa.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.hasversion.spa.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
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.local.spa.fl_str_mv |
Artículo de investigación |
format |
http://purl.org/coar/resource_type/c_2df8fbb1 |
status_str |
publishedVersion |
dc.identifier.citation.spa.fl_str_mv |
Quiliano M, Mendoza A, Fong KY, Pabón A, Goldfarb NE, Fabing I, Vettorazzi A, López de Cerain A, Dunn BM, Garavito G, Wright DW, Deharo E, Pérez-Silanes S, Aldana I, Galiano S. Exploring the scope of new arylamino alcohol derivatives: Synthesis, antimalarial evaluation, toxicological studies, and target exploration. Int J Parasitol Drugs Drug Resist. 2016 Dec;6(3):184-198. doi: 10.1016/j.ijpddr.2016.09.004. |
dc.identifier.issn.none.fl_str_mv |
2211-3207 |
dc.identifier.uri.none.fl_str_mv |
https://hdl.handle.net/10495/32004 |
dc.identifier.doi.none.fl_str_mv |
10.1016/j.ijpddr.2016.09.004 |
identifier_str_mv |
Quiliano M, Mendoza A, Fong KY, Pabón A, Goldfarb NE, Fabing I, Vettorazzi A, López de Cerain A, Dunn BM, Garavito G, Wright DW, Deharo E, Pérez-Silanes S, Aldana I, Galiano S. Exploring the scope of new arylamino alcohol derivatives: Synthesis, antimalarial evaluation, toxicological studies, and target exploration. Int J Parasitol Drugs Drug Resist. 2016 Dec;6(3):184-198. doi: 10.1016/j.ijpddr.2016.09.004. 2211-3207 10.1016/j.ijpddr.2016.09.004 |
url |
https://hdl.handle.net/10495/32004 |
dc.language.iso.spa.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartofjournalabbrev.spa.fl_str_mv |
Int. J. Parasitol. Drugs Drug Resist. |
dc.rights.spa.fl_str_mv |
info:eu-repo/semantics/openAccess |
dc.rights.uri.*.fl_str_mv |
http://creativecommons.org/licenses/by-nc-nd/2.5/co/ |
dc.rights.accessrights.spa.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.creativecommons.spa.fl_str_mv |
https://creativecommons.org/licenses/by-nc-nd/4.0/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by-nc-nd/2.5/co/ http://purl.org/coar/access_right/c_abf2 https://creativecommons.org/licenses/by-nc-nd/4.0/ |
dc.format.extent.spa.fl_str_mv |
15 |
dc.format.mimetype.spa.fl_str_mv |
application/pdf |
dc.publisher.spa.fl_str_mv |
Elsevier |
dc.publisher.group.spa.fl_str_mv |
Grupo Malaria |
dc.publisher.place.spa.fl_str_mv |
Ámsterdam, Países Bajos |
institution |
Universidad de Antioquia |
bitstream.url.fl_str_mv |
https://bibliotecadigital.udea.edu.co/bitstream/10495/32004/1/PabonAdriana_2016_ExploringAntimalarialEvaluation.pdf https://bibliotecadigital.udea.edu.co/bitstream/10495/32004/2/license_rdf https://bibliotecadigital.udea.edu.co/bitstream/10495/32004/3/license.txt |
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bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 MD5 |
repository.name.fl_str_mv |
Repositorio Institucional Universidad de Antioquia |
repository.mail.fl_str_mv |
andres.perez@udea.edu.co |
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1812173157256134656 |
spelling |
Pabón Vidal, Adriana LucíaQuiliano, MiguelMendoza, AdelaFong, KimGoldfarb, NathanFabing, IsabelleVettorazzi, ArianeLópez de Cerain, AdelaDunn, BenGaravito, GiovannyWright, DavidDeHaro, EricPérez Silanes, SilviaAldana, IgnacioGaliano, Silvia2022-11-13T16:01:20Z2022-11-13T16:01:20Z2016Quiliano M, Mendoza A, Fong KY, Pabón A, Goldfarb NE, Fabing I, Vettorazzi A, López de Cerain A, Dunn BM, Garavito G, Wright DW, Deharo E, Pérez-Silanes S, Aldana I, Galiano S. Exploring the scope of new arylamino alcohol derivatives: Synthesis, antimalarial evaluation, toxicological studies, and target exploration. Int J Parasitol Drugs Drug Resist. 2016 Dec;6(3):184-198. doi: 10.1016/j.ijpddr.2016.09.004.2211-3207https://hdl.handle.net/10495/3200410.1016/j.ijpddr.2016.09.004ABSTRACT: Synthesis of new 1-aryl-3-substituted propanol derivatives followed by structure-activity relationship, in silico drug-likeness, cytotoxicity, genotoxicity, in silico metabolism, in silico pharmacophore modeling, and in vivo studies led to the identification of compounds 22 and 23 with significant in vitro antiplasmodial activity against drug sensitive (D6 IC50 ≤ 0.19 μM) and multidrug resistant (FCR-3 IC50 ≤ 0.40 μM and C235 IC50 ≤ 0.28 μM) strains of Plasmodium falciparum. Adequate selectivity index and absence of genotoxicity was also observed. Notably, compound 22 displays excellent parasitemia reduction (98 ± 1%), and complete cure with all treated mice surviving through the entire period with no signs of toxicity. One important factor is the agreement between in vitro potency and in vivo studies. Target exploration was performed; this chemotype series exhibits an alternative antimalarial mechanism.COL000752415application/pdfengElsevierGrupo MalariaÁmsterdam, Países Bajosinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARTArtículo de investigaciónhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-nd/2.5/co/http://purl.org/coar/access_right/c_abf2https://creativecommons.org/licenses/by-nc-nd/4.0/Drug-Related Side Effects and Adverse ReactionsAntimaláricosAntimalarialsAmino AlcoholesAmino AlcoholsModelos Animales de EnfermedadDisease Models, AnimalConcentración 50 InhibidoraInhibitory Concentration 50Malaria FalciparumMalaria, FalciparumPlasmodium falciparumRelación Estructura-ActividadStructure-Activity RelationshipResultado del TratamientoTreatment OutcomeAnálisis de SupervivenciaSurvival AnalysisRatonesMicehttp://id.nlm.nih.gov/mesh/D064420Exploring the scope of new arylamino alcohol derivatives: Synthesis, antimalarial evaluation, toxicological studies, and target explorationInt. J. Parasitol. Drugs Drug Resist.International Journal for Parasitology: Drugs and Drug Resistance18419863ORIGINALPabonAdriana_2016_ExploringAntimalarialEvaluation.pdfPabonAdriana_2016_ExploringAntimalarialEvaluation.pdfArtículo de investigaciónapplication/pdf1758584https://bibliotecadigital.udea.edu.co/bitstream/10495/32004/1/PabonAdriana_2016_ExploringAntimalarialEvaluation.pdf6abf3b744cd63444c4e0dd8b18f8303fMD51CC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8823https://bibliotecadigital.udea.edu.co/bitstream/10495/32004/2/license_rdfb88b088d9957e670ce3b3fbe2eedbc13MD52LICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://bibliotecadigital.udea.edu.co/bitstream/10495/32004/3/license.txt8a4605be74aa9ea9d79846c1fba20a33MD5310495/32004oai:bibliotecadigital.udea.edu.co:10495/320042022-11-13 11:01:21.358Repositorio Institucional Universidad de Antioquiaandres.perez@udea.edu.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 |