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/
Summary: | 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. |
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