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...
- 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/
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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 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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1812173256272117760 |
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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 |