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...

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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/
id UDEA2_0d63e3f3ec56d28994569e77b5975a5d
oai_identifier_str oai:bibliotecadigital.udea.edu.co:10495/32004
network_acronym_str UDEA2
network_name_str Repositorio UdeA
repository_id_str
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
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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
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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
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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
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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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