Synthesis, Leishmanicidal and Cytotoxic Activity of Triclosan-Chalcone, Triclosan-Chromone and Triclosan-Coumarin Hybrids

ABSTRACT: Twelve hybrids derived from triclosan were obtained via Williamson etherification of O-triclosan alkyl bromide plus chalcone and O-coumarin or O-chromone alkyl bromide plus triclosan, respectively. Structures of the products were elucidated by spectroscopic analysis. The synthesized compou...

Full description

Autores:
Otero Tejada, Elver Luis
Vergara Guiral, Sebastian
Robledo Restrepo, Sara María
Cardona Galeano, Wilson
Carda Usó, Pedro Miguel
Vélez Bernal, Iván Darío
Rojas Arbeláez, Carlos Alberto
Otálvaro Tamayo, Felipe
Tipo de recurso:
Article of investigation
Fecha de publicación:
2014
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/23678
Acceso en línea:
http://hdl.handle.net/10495/23678
Palabra clave:
Triclosan
Triclosán
Chalcone
Chalcona
Leishmaniasis
Antimicrobial properties
Propiedades antimicrobianas
Coumarins
Cumarinas
Hybrids
Híbridos
http://aims.fao.org/aos/agrovoc/c_35197
http://aims.fao.org/aos/agrovoc/c_26756
http://aims.fao.org/aos/agrovoc/c_1933
http://aims.fao.org/aos/agrovoc/c_3707
Rights
openAccess
License
http://creativecommons.org/licenses/by/2.5/co/
id UDEA2_5731262b18c7cd139daed8ed4fcb5bfd
oai_identifier_str oai:bibliotecadigital.udea.edu.co:10495/23678
network_acronym_str UDEA2
network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv Synthesis, Leishmanicidal and Cytotoxic Activity of Triclosan-Chalcone, Triclosan-Chromone and Triclosan-Coumarin Hybrids
title Synthesis, Leishmanicidal and Cytotoxic Activity of Triclosan-Chalcone, Triclosan-Chromone and Triclosan-Coumarin Hybrids
spellingShingle Synthesis, Leishmanicidal and Cytotoxic Activity of Triclosan-Chalcone, Triclosan-Chromone and Triclosan-Coumarin Hybrids
Triclosan
Triclosán
Chalcone
Chalcona
Leishmaniasis
Antimicrobial properties
Propiedades antimicrobianas
Coumarins
Cumarinas
Hybrids
Híbridos
http://aims.fao.org/aos/agrovoc/c_35197
http://aims.fao.org/aos/agrovoc/c_26756
http://aims.fao.org/aos/agrovoc/c_1933
http://aims.fao.org/aos/agrovoc/c_3707
title_short Synthesis, Leishmanicidal and Cytotoxic Activity of Triclosan-Chalcone, Triclosan-Chromone and Triclosan-Coumarin Hybrids
title_full Synthesis, Leishmanicidal and Cytotoxic Activity of Triclosan-Chalcone, Triclosan-Chromone and Triclosan-Coumarin Hybrids
title_fullStr Synthesis, Leishmanicidal and Cytotoxic Activity of Triclosan-Chalcone, Triclosan-Chromone and Triclosan-Coumarin Hybrids
title_full_unstemmed Synthesis, Leishmanicidal and Cytotoxic Activity of Triclosan-Chalcone, Triclosan-Chromone and Triclosan-Coumarin Hybrids
title_sort Synthesis, Leishmanicidal and Cytotoxic Activity of Triclosan-Chalcone, Triclosan-Chromone and Triclosan-Coumarin Hybrids
dc.creator.fl_str_mv Otero Tejada, Elver Luis
Vergara Guiral, Sebastian
Robledo Restrepo, Sara María
Cardona Galeano, Wilson
Carda Usó, Pedro Miguel
Vélez Bernal, Iván Darío
Rojas Arbeláez, Carlos Alberto
Otálvaro Tamayo, Felipe
dc.contributor.author.none.fl_str_mv Otero Tejada, Elver Luis
Vergara Guiral, Sebastian
Robledo Restrepo, Sara María
Cardona Galeano, Wilson
Carda Usó, Pedro Miguel
Vélez Bernal, Iván Darío
Rojas Arbeláez, Carlos Alberto
Otálvaro Tamayo, Felipe
dc.subject.decs.none.fl_str_mv Triclosan
Triclosán
Chalcone
Chalcona
topic Triclosan
Triclosán
Chalcone
Chalcona
Leishmaniasis
Antimicrobial properties
Propiedades antimicrobianas
Coumarins
Cumarinas
Hybrids
Híbridos
http://aims.fao.org/aos/agrovoc/c_35197
http://aims.fao.org/aos/agrovoc/c_26756
http://aims.fao.org/aos/agrovoc/c_1933
http://aims.fao.org/aos/agrovoc/c_3707
dc.subject.agrovoc.none.fl_str_mv Leishmaniasis
Antimicrobial properties
Propiedades antimicrobianas
Coumarins
Cumarinas
Hybrids
Híbridos
dc.subject.agrovocuri.none.fl_str_mv http://aims.fao.org/aos/agrovoc/c_35197
http://aims.fao.org/aos/agrovoc/c_26756
http://aims.fao.org/aos/agrovoc/c_1933
dc.subject.lcshuri.none.fl_str_mv http://aims.fao.org/aos/agrovoc/c_3707
description ABSTRACT: Twelve hybrids derived from triclosan were obtained via Williamson etherification of O-triclosan alkyl bromide plus chalcone and O-coumarin or O-chromone alkyl bromide plus triclosan, respectively. Structures of the products were elucidated by spectroscopic analysis. The synthesized compounds were evaluated for antileishmanial activity against L. (V) panamensis amastigotes. Cytotoxic activity was also evaluated against mammalian U-937 cells. Compounds 7–9 and 17, were active against Leishmania parasites (EC50 = 9.4; 10.2; 13.5 and 27.5 µg/mL, respectively) and showed no toxicity toward mammalian cells (>200 µg/mL). They are potential candidates for antileishmanial drug development. Compounds 25–27, were active and cytotoxic. Further studies using other cell types are needed in order to discriminate whether the toxicity shown by these compounds is against tumor or non-tumor cells. The results indicate that compounds containing small alkyl chains show better selectivity indices. Moreover, Michael acceptor moieties may modify both the leishmanicidal activity and cytotoxicity. Further studies are required to evaluate if the in vitro activity against Leishmania panamensis demonstrated here is also observed in vivo.
publishDate 2014
dc.date.issued.none.fl_str_mv 2014
dc.date.accessioned.none.fl_str_mv 2021-11-01T21:43:54Z
dc.date.available.none.fl_str_mv 2021-11-01T21:43:54Z
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 Otero, E., Vergara, S., Robledo, S., Cardona, W., Carda, M., Vélez, I., Rojas, C & Otálvaro, F. (2014). Synthesis, Leishmanicidal and Cytotoxic Activity of Triclosan-Chalcone, Triclosan-Chromone and Triclosan-Coumarin Hybrids. Molecules, 19(9), 13251–13266. doi:10.3390/molecules190913251
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/10495/23678
dc.identifier.doi.none.fl_str_mv 10.3390/molecules190913251
dc.identifier.eissn.none.fl_str_mv 1420-3049
identifier_str_mv Otero, E., Vergara, S., Robledo, S., Cardona, W., Carda, M., Vélez, I., Rojas, C & Otálvaro, F. (2014). Synthesis, Leishmanicidal and Cytotoxic Activity of Triclosan-Chalcone, Triclosan-Chromone and Triclosan-Coumarin Hybrids. Molecules, 19(9), 13251–13266. doi:10.3390/molecules190913251
10.3390/molecules190913251
1420-3049
url http://hdl.handle.net/10495/23678
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Molecules
dc.rights.spa.fl_str_mv info:eu-repo/semantics/openAccess
dc.rights.uri.*.fl_str_mv http://creativecommons.org/licenses/by/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/4.0/
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/2.5/co/
http://purl.org/coar/access_right/c_abf2
https://creativecommons.org/licenses/by/4.0/
dc.format.extent.spa.fl_str_mv 16
dc.format.mimetype.spa.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv MDPI
dc.publisher.group.spa.fl_str_mv Programa de Estudio y Control de Enfermedades Tropicales (PECET)
Química de Plantas Colombianas
Síntesis y Biosíntesis de Metabolitos Naturales
dc.publisher.place.spa.fl_str_mv Basilea, Suiza
institution Universidad de Antioquia
bitstream.url.fl_str_mv http://bibliotecadigital.udea.edu.co/bitstream/10495/23678/3/license.txt
http://bibliotecadigital.udea.edu.co/bitstream/10495/23678/1/OteroElver_2014_LeishmanicidalCytotoxicTriclosan.pdf
http://bibliotecadigital.udea.edu.co/bitstream/10495/23678/2/license_rdf
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bitstream.checksumAlgorithm.fl_str_mv MD5
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repository.name.fl_str_mv Repositorio Institucional Universidad de Antioquia
repository.mail.fl_str_mv andres.perez@udea.edu.co
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spelling Otero Tejada, Elver LuisVergara Guiral, SebastianRobledo Restrepo, Sara MaríaCardona Galeano, WilsonCarda Usó, Pedro MiguelVélez Bernal, Iván DaríoRojas Arbeláez, Carlos AlbertoOtálvaro Tamayo, Felipe2021-11-01T21:43:54Z2021-11-01T21:43:54Z2014Otero, E., Vergara, S., Robledo, S., Cardona, W., Carda, M., Vélez, I., Rojas, C & Otálvaro, F. (2014). Synthesis, Leishmanicidal and Cytotoxic Activity of Triclosan-Chalcone, Triclosan-Chromone and Triclosan-Coumarin Hybrids. Molecules, 19(9), 13251–13266. doi:10.3390/molecules190913251http://hdl.handle.net/10495/2367810.3390/molecules1909132511420-3049ABSTRACT: Twelve hybrids derived from triclosan were obtained via Williamson etherification of O-triclosan alkyl bromide plus chalcone and O-coumarin or O-chromone alkyl bromide plus triclosan, respectively. Structures of the products were elucidated by spectroscopic analysis. The synthesized compounds were evaluated for antileishmanial activity against L. (V) panamensis amastigotes. Cytotoxic activity was also evaluated against mammalian U-937 cells. Compounds 7–9 and 17, were active against Leishmania parasites (EC50 = 9.4; 10.2; 13.5 and 27.5 µg/mL, respectively) and showed no toxicity toward mammalian cells (>200 µg/mL). They are potential candidates for antileishmanial drug development. Compounds 25–27, were active and cytotoxic. Further studies using other cell types are needed in order to discriminate whether the toxicity shown by these compounds is against tumor or non-tumor cells. The results indicate that compounds containing small alkyl chains show better selectivity indices. Moreover, Michael acceptor moieties may modify both the leishmanicidal activity and cytotoxicity. Further studies are required to evaluate if the in vitro activity against Leishmania panamensis demonstrated here is also observed in vivo.COL0069689COL0015099COL001532916application/pdfengMDPIPrograma de Estudio y Control de Enfermedades Tropicales (PECET)Química de Plantas ColombianasSíntesis y Biosíntesis de Metabolitos NaturalesBasilea, Suizainfo: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/2.5/co/http://purl.org/coar/access_right/c_abf2https://creativecommons.org/licenses/by/4.0/Synthesis, Leishmanicidal and Cytotoxic Activity of Triclosan-Chalcone, Triclosan-Chromone and Triclosan-Coumarin HybridsTriclosanTriclosánChalconeChalconaLeishmaniasisAntimicrobial propertiesPropiedades antimicrobianasCoumarinsCumarinasHybridsHíbridoshttp://aims.fao.org/aos/agrovoc/c_35197http://aims.fao.org/aos/agrovoc/c_26756http://aims.fao.org/aos/agrovoc/c_1933http://aims.fao.org/aos/agrovoc/c_3707MoleculesMolecules1325113266199LICENSElicense.txtlicense.txttext/plain; charset=utf-81748http://bibliotecadigital.udea.edu.co/bitstream/10495/23678/3/license.txt8a4605be74aa9ea9d79846c1fba20a33MD53ORIGINALOteroElver_2014_LeishmanicidalCytotoxicTriclosan.pdfOteroElver_2014_LeishmanicidalCytotoxicTriclosan.pdfArtículo de investigaciónapplication/pdf846299http://bibliotecadigital.udea.edu.co/bitstream/10495/23678/1/OteroElver_2014_LeishmanicidalCytotoxicTriclosan.pdf06ce22493e2d023dd79baafbcfa8f867MD51CC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8927http://bibliotecadigital.udea.edu.co/bitstream/10495/23678/2/license_rdf1646d1f6b96dbbbc38035efc9239ac9cMD5210495/23678oai:bibliotecadigital.udea.edu.co:10495/236782021-11-01 16:43:55.237Repositorio Institucional Universidad de Antioquiaandres.perez@udea.edu.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