Tyrosol and hydroxytyrosol derivatives as antitrypanosomal and antileishmanial agents

Trypanosomiasis and leishmaniasis keep being a real challenge for health and development of African countries. Existing treatments have considerable side effects and increase resistance of the parasites. We have measured antitrypanosomal and antileishmanial activity of natural phenols, tyrosol (TYR)...

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Detalles Bibliográficos
Autores: Belmonte Reche, Efres, Martínez García, Marta, Peñalver, Pablo, Gómez Pérez, Verónica, Lucas Rodríguez, Ricardo, Gamarro, Francisco, Pérez Victoria, José María, Morales, Juan Carlos
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2016
País:España
Institución:Universidad de Sevilla (US)
Repositorio:idUS. Depósito de Investigación de la Universidad de Sevilla
OAI Identifier:oai:idus.us.es:11441/135176
Acceso en línea:https://hdl.handle.net/11441/135176
https://doi.org/10.1016/j.ejmech.2016.04.047
Access Level:acceso abierto
Palabra clave:Antileishmanial
Antitrypanosomal
Hydroxytyrosol
Tyrosol
Descripción
Sumario:Trypanosomiasis and leishmaniasis keep being a real challenge for health and development of African countries. Existing treatments have considerable side effects and increase resistance of the parasites. We have measured antitrypanosomal and antileishmanial activity of natural phenols, tyrosol (TYR) and hydroxytyrosol (HT) and several of their esters and metabolites. We found significant IC50 values against Trypanosoma brucei for HT decanoate ester and HT dodecanoate ester (0.6 and 0.36 μM, respectively). This represents a large increase in activity with respect to HT (79 and 132 fold, respectively). Moreover, both compounds displayed a high selectivity index against MRC-5, a non-tumoral human cell line (118 and 106, respectively). Then, we synthesized a focused library of compounds to explore structure-activity. We found the ether and thiourea analogs of HT decanoate ester and HT dodecanoate ester also showed IC50 values against T. brucei in the low micromolar range. In conclusion, the di-ortho phenolic ring and medium size alkyl chain are essential for activity whereas the nature of the chemical bond among them seems less important.