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- W2345492080 abstract "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." @default.
- W2345492080 created "2016-06-24" @default.
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- W2345492080 date "2016-08-01" @default.
- W2345492080 modified "2023-10-15" @default.
- W2345492080 title "Tyrosol and hydroxytyrosol derivatives as antitrypanosomal and antileishmanial agents" @default.
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- W2345492080 doi "https://doi.org/10.1016/j.ejmech.2016.04.047" @default.
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