Synthesis, antiprotozoal activity and cytotoxicity in U-937 macrophages of triclosan–hydrazone hybrids
ABSTRACT: The synthesis and biological activities (cytotoxicity, leishmanicidal, and trypanocidal) of 11 triclosan–hydrazone hybrids are described herein. The structure of the products was elucidated by spectral data (NMR, IR) and mass spectrometric analyses. The synthesized compounds were evaluated...
- Autores:
-
Vergara Guira, Sebastian
Carda, Miguel
Agut, Raül
Yepes Daza, Lina Marcela
Vélez Bernal, Iván Darío
Robledo Restrepo, Sara María
Cardona Galeano, Wilson
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2017
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/23345
- Acceso en línea:
- http://hdl.handle.net/10495/23345
- Palabra clave:
- Leishmaniasis
Enfermedad de Chagas
Chagas Disease
Trypanosoma cruzi
Triclosán
Triclosan
- Rights
- openAccess
- License
- http://creativecommons.org/licenses/by/2.5/co/
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| dc.title.spa.fl_str_mv |
Synthesis, antiprotozoal activity and cytotoxicity in U-937 macrophages of triclosan–hydrazone hybrids |
| title |
Synthesis, antiprotozoal activity and cytotoxicity in U-937 macrophages of triclosan–hydrazone hybrids |
| spellingShingle |
Synthesis, antiprotozoal activity and cytotoxicity in U-937 macrophages of triclosan–hydrazone hybrids Leishmaniasis Enfermedad de Chagas Chagas Disease Trypanosoma cruzi Triclosán Triclosan |
| title_short |
Synthesis, antiprotozoal activity and cytotoxicity in U-937 macrophages of triclosan–hydrazone hybrids |
| title_full |
Synthesis, antiprotozoal activity and cytotoxicity in U-937 macrophages of triclosan–hydrazone hybrids |
| title_fullStr |
Synthesis, antiprotozoal activity and cytotoxicity in U-937 macrophages of triclosan–hydrazone hybrids |
| title_full_unstemmed |
Synthesis, antiprotozoal activity and cytotoxicity in U-937 macrophages of triclosan–hydrazone hybrids |
| title_sort |
Synthesis, antiprotozoal activity and cytotoxicity in U-937 macrophages of triclosan–hydrazone hybrids |
| dc.creator.fl_str_mv |
Vergara Guira, Sebastian Carda, Miguel Agut, Raül Yepes Daza, Lina Marcela Vélez Bernal, Iván Darío Robledo Restrepo, Sara María Cardona Galeano, Wilson |
| dc.contributor.author.none.fl_str_mv |
Vergara Guira, Sebastian Carda, Miguel Agut, Raül Yepes Daza, Lina Marcela Vélez Bernal, Iván Darío Robledo Restrepo, Sara María Cardona Galeano, Wilson |
| dc.contributor.researchgroup.spa.fl_str_mv |
Programa de Estudio y Control de Enfermedades Tropicales (PECET) Química de Plantas Colombianas |
| dc.subject.decs.none.fl_str_mv |
Leishmaniasis Enfermedad de Chagas Chagas Disease Trypanosoma cruzi Triclosán Triclosan |
| topic |
Leishmaniasis Enfermedad de Chagas Chagas Disease Trypanosoma cruzi Triclosán Triclosan |
| description |
ABSTRACT: The synthesis and biological activities (cytotoxicity, leishmanicidal, and trypanocidal) of 11 triclosan–hydrazone hybrids are described herein. The structure of the products was elucidated by spectral data (NMR, IR) and mass spectrometric analyses. The synthesized compounds were evaluated against amastigotes forms of L. (V) panamensis, which is the most prevalent Leish-mania species in Colombia, and against Trypanosoma cruzi, which is the major pathogenic species to Chagas disease in humans. In addition, the cytotoxic activity of the synthesized compounds was evaluated against human U- 937 macrophages. Hydrazone hybrids were obtained as Esynperiplanar and E-antiperiplanar conformers. Nine of them were active against L. (V) panamensis (5a–5d, 5f–5j) and eight of them against T. cruzi (5a, 5c, 5d, 5f–5j), with EC50 values lower than 40 μM. The compounds 5c, 5e, and 5h exhibit the best selectivity index against both L. (V) panamensis and T. cruzi, with values ranging from 5.90 to 16.55, thus showing potential as starting compounds for the eventual development of drugs against these parasites. The presence of hydroxy or methoxy groups in positions 2 and 4 of the aromatic ring of the benzylidene moiety increases both activity and cytotoxicity. There is no clear relationship between the antiprotozoal activity and the methylation pattern of the hydroxy groups, since in some cases methylation decreases the activity (5d vs. 5g) while in other cases the activity is increased (5c vs. 5f and 5i vs. 5j). |
| publishDate |
2017 |
| dc.date.issued.none.fl_str_mv |
2017 |
| dc.date.accessioned.none.fl_str_mv |
2021-10-21T15:04:37Z |
| dc.date.available.none.fl_str_mv |
2021-10-21T15:04:37Z |
| dc.type.spa.fl_str_mv |
Artículo de investigación |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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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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1054-2523 |
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http://hdl.handle.net/10495/23345 |
| dc.identifier.doi.none.fl_str_mv |
10.1007/s00044-017-2019-2 |
| dc.identifier.eissn.none.fl_str_mv |
1554-8120 |
| identifier_str_mv |
1054-2523 10.1007/s00044-017-2019-2 1554-8120 |
| url |
http://hdl.handle.net/10495/23345 |
| dc.language.iso.spa.fl_str_mv |
eng |
| language |
eng |
| dc.relation.ispartofjournalabbrev.spa.fl_str_mv |
Med. Chem. Res. |
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12 |
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1 |
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Medicinal Chemistry Research |
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http://creativecommons.org/licenses/by/2.5/co/ |
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Springer |
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Vergara Guira, SebastianCarda, MiguelAgut, RaülYepes Daza, Lina MarcelaVélez Bernal, Iván DaríoRobledo Restrepo, Sara MaríaCardona Galeano, WilsonPrograma de Estudio y Control de Enfermedades Tropicales (PECET)Química de Plantas Colombianas2021-10-21T15:04:37Z2021-10-21T15:04:37Z20171054-2523http://hdl.handle.net/10495/2334510.1007/s00044-017-2019-21554-8120ABSTRACT: The synthesis and biological activities (cytotoxicity, leishmanicidal, and trypanocidal) of 11 triclosan–hydrazone hybrids are described herein. The structure of the products was elucidated by spectral data (NMR, IR) and mass spectrometric analyses. The synthesized compounds were evaluated against amastigotes forms of L. (V) panamensis, which is the most prevalent Leish-mania species in Colombia, and against Trypanosoma cruzi, which is the major pathogenic species to Chagas disease in humans. In addition, the cytotoxic activity of the synthesized compounds was evaluated against human U- 937 macrophages. Hydrazone hybrids were obtained as Esynperiplanar and E-antiperiplanar conformers. Nine of them were active against L. (V) panamensis (5a–5d, 5f–5j) and eight of them against T. cruzi (5a, 5c, 5d, 5f–5j), with EC50 values lower than 40 μM. The compounds 5c, 5e, and 5h exhibit the best selectivity index against both L. (V) panamensis and T. cruzi, with values ranging from 5.90 to 16.55, thus showing potential as starting compounds for the eventual development of drugs against these parasites. The presence of hydroxy or methoxy groups in positions 2 and 4 of the aromatic ring of the benzylidene moiety increases both activity and cytotoxicity. There is no clear relationship between the antiprotozoal activity and the methylation pattern of the hydroxy groups, since in some cases methylation decreases the activity (5d vs. 5g) while in other cases the activity is increased (5c vs. 5f and 5i vs. 5j).COL0015099COL001532912application/pdfengSpringerNueva York, Estados Unidoshttp://creativecommons.org/licenses/by/2.5/co/https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Synthesis, antiprotozoal activity and cytotoxicity in U-937 macrophages of triclosan–hydrazone hybridsArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionLeishmaniasisEnfermedad de ChagasChagas DiseaseTrypanosoma cruziTriclosánTriclosanMed. Chem. 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