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:
- Antiprotozoario
Antiprotozoal Agents
Triclosán
Triclosan
Cumarinas
Coumarins
Cromonas
Chromones
Chalcona
Chalcone
Leishmaniosis
Híbrido
Hybrids
http://aims.fao.org/aos/agrovoc/c_35197
http://aims.fao.org/aos/agrovoc/c_3707
https://id.nlm.nih.gov/mesh/D000981
https://id.nlm.nih.gov/mesh/D014260
https://id.nlm.nih.gov/mesh/D003374
https://id.nlm.nih.gov/mesh/D002867
https://id.nlm.nih.gov/mesh/D002599
- Rights
- openAccess
- License
- http://creativecommons.org/licenses/by/2.5/co/
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| 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 Antiprotozoario Antiprotozoal Agents Triclosán Triclosan Cumarinas Coumarins Cromonas Chromones Chalcona Chalcone Leishmaniosis Híbrido Hybrids http://aims.fao.org/aos/agrovoc/c_35197 http://aims.fao.org/aos/agrovoc/c_3707 https://id.nlm.nih.gov/mesh/D000981 https://id.nlm.nih.gov/mesh/D014260 https://id.nlm.nih.gov/mesh/D003374 https://id.nlm.nih.gov/mesh/D002867 https://id.nlm.nih.gov/mesh/D002599 |
| 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.contributor.researchgroup.spa.fl_str_mv |
Programa de Estudio y Control de Enfermedades Tropicales (PECET) Química de Plantas Colombianas Síntesis y Biosíntesis de Metabolitos Naturales |
| dc.subject.decs.none.fl_str_mv |
Antiprotozoario Antiprotozoal Agents Triclosán Triclosan Cumarinas Coumarins Cromonas Chromones Chalcona Chalcone |
| topic |
Antiprotozoario Antiprotozoal Agents Triclosán Triclosan Cumarinas Coumarins Cromonas Chromones Chalcona Chalcone Leishmaniosis Híbrido Hybrids http://aims.fao.org/aos/agrovoc/c_35197 http://aims.fao.org/aos/agrovoc/c_3707 https://id.nlm.nih.gov/mesh/D000981 https://id.nlm.nih.gov/mesh/D014260 https://id.nlm.nih.gov/mesh/D003374 https://id.nlm.nih.gov/mesh/D002867 https://id.nlm.nih.gov/mesh/D002599 |
| dc.subject.agrovoc.none.fl_str_mv |
Leishmaniosis Híbrido Hybrids |
| dc.subject.agrovocuri.none.fl_str_mv |
http://aims.fao.org/aos/agrovoc/c_35197 http://aims.fao.org/aos/agrovoc/c_3707 |
| dc.subject.meshuri.none.fl_str_mv |
https://id.nlm.nih.gov/mesh/D000981 https://id.nlm.nih.gov/mesh/D014260 https://id.nlm.nih.gov/mesh/D003374 https://id.nlm.nih.gov/mesh/D002867 https://id.nlm.nih.gov/mesh/D002599 |
| 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 |
Artículo de investigación |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
| dc.type.redcol.spa.fl_str_mv |
https://purl.org/redcol/resource_type/ART |
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http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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info:eu-repo/semantics/article |
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info:eu-repo/semantics/publishedVersion |
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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 |
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eng |
| language |
eng |
| dc.relation.ispartofjournalabbrev.spa.fl_str_mv |
Molecules |
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13266 |
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9 |
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13251 |
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19 |
| dc.relation.ispartofjournal.spa.fl_str_mv |
Molecules |
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http://creativecommons.org/licenses/by/2.5/co/ |
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Otero Tejada, Elver LuisVergara Guiral, SebastianRobledo Restrepo, Sara MaríaCardona Galeano, WilsonCarda Usó, Pedro MiguelVélez Bernal, Iván DaríoRojas Arbeláez, Carlos AlbertoOtálvaro Tamayo, FelipePrograma de Estudio y Control de Enfermedades Tropicales (PECET)Química de Plantas ColombianasSíntesis y Biosíntesis de Metabolitos Naturales2021-11-01T21:43:54Z2021-11-01T21:43:54Z2014Otero, 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. 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