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Synthesis and In Vitro Anti Leishmania amazonensis Biological Screening of Morita-Baylis-Hillman Adducts Prepared from Eugenol, Thymol and Carvacrol

Leishmaniasis represents a series of severe neglected tropical diseases caused by protozoa of the genus Leishmania and is widely distributed around the world. Here, we present the syntheses of Morita-Baylis-Hillman adducts (MBHAs) prepared from eugenol, thymol and carvacrol, and their bioevaluation...

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Autores principales: Xavier, Francisco José Seixas, Rodrigues, Klinger Antonio da Franca, de Oliveira, Ramon Guerra, Lima Junior, Claudio Gabriel, Rocha, Juliana da Câmara, Keesen, Tatjana Souza Lima, de Oliveira, Marcia Rosa, Silva, Fábio Pedrosa Lins, Vasconcellos, Mário Luiz Araújo de Almeida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274563/
https://www.ncbi.nlm.nih.gov/pubmed/27834831
http://dx.doi.org/10.3390/molecules21111483
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author Xavier, Francisco José Seixas
Rodrigues, Klinger Antonio da Franca
de Oliveira, Ramon Guerra
Lima Junior, Claudio Gabriel
Rocha, Juliana da Câmara
Keesen, Tatjana Souza Lima
de Oliveira, Marcia Rosa
Silva, Fábio Pedrosa Lins
Vasconcellos, Mário Luiz Araújo de Almeida
author_facet Xavier, Francisco José Seixas
Rodrigues, Klinger Antonio da Franca
de Oliveira, Ramon Guerra
Lima Junior, Claudio Gabriel
Rocha, Juliana da Câmara
Keesen, Tatjana Souza Lima
de Oliveira, Marcia Rosa
Silva, Fábio Pedrosa Lins
Vasconcellos, Mário Luiz Araújo de Almeida
author_sort Xavier, Francisco José Seixas
collection PubMed
description Leishmaniasis represents a series of severe neglected tropical diseases caused by protozoa of the genus Leishmania and is widely distributed around the world. Here, we present the syntheses of Morita-Baylis-Hillman adducts (MBHAs) prepared from eugenol, thymol and carvacrol, and their bioevaluation against promastigotes of Leishmania amazonensis. The new MBHAs are prepared in two steps from essential oils in moderate to good yields and present IC(50) values in the range of 22.30–4.71 μM. Moreover, the selectivity index to the most potent compound is very high (SIrb > 84.92), far better than that of Glucantime(®) (SIrb 1.39) and amphotericin B (SIrb = 22.34). Conformational analysis were carried out at the M062X//6-31+G(d,p) level of theory to corroborate a hypothesis about the nitroaromatic bioreduction mechanism.
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spelling pubmed-62745632018-12-28 Synthesis and In Vitro Anti Leishmania amazonensis Biological Screening of Morita-Baylis-Hillman Adducts Prepared from Eugenol, Thymol and Carvacrol Xavier, Francisco José Seixas Rodrigues, Klinger Antonio da Franca de Oliveira, Ramon Guerra Lima Junior, Claudio Gabriel Rocha, Juliana da Câmara Keesen, Tatjana Souza Lima de Oliveira, Marcia Rosa Silva, Fábio Pedrosa Lins Vasconcellos, Mário Luiz Araújo de Almeida Molecules Article Leishmaniasis represents a series of severe neglected tropical diseases caused by protozoa of the genus Leishmania and is widely distributed around the world. Here, we present the syntheses of Morita-Baylis-Hillman adducts (MBHAs) prepared from eugenol, thymol and carvacrol, and their bioevaluation against promastigotes of Leishmania amazonensis. The new MBHAs are prepared in two steps from essential oils in moderate to good yields and present IC(50) values in the range of 22.30–4.71 μM. Moreover, the selectivity index to the most potent compound is very high (SIrb > 84.92), far better than that of Glucantime(®) (SIrb 1.39) and amphotericin B (SIrb = 22.34). Conformational analysis were carried out at the M062X//6-31+G(d,p) level of theory to corroborate a hypothesis about the nitroaromatic bioreduction mechanism. MDPI 2016-11-08 /pmc/articles/PMC6274563/ /pubmed/27834831 http://dx.doi.org/10.3390/molecules21111483 Text en © 2016 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Xavier, Francisco José Seixas
Rodrigues, Klinger Antonio da Franca
de Oliveira, Ramon Guerra
Lima Junior, Claudio Gabriel
Rocha, Juliana da Câmara
Keesen, Tatjana Souza Lima
de Oliveira, Marcia Rosa
Silva, Fábio Pedrosa Lins
Vasconcellos, Mário Luiz Araújo de Almeida
Synthesis and In Vitro Anti Leishmania amazonensis Biological Screening of Morita-Baylis-Hillman Adducts Prepared from Eugenol, Thymol and Carvacrol
title Synthesis and In Vitro Anti Leishmania amazonensis Biological Screening of Morita-Baylis-Hillman Adducts Prepared from Eugenol, Thymol and Carvacrol
title_full Synthesis and In Vitro Anti Leishmania amazonensis Biological Screening of Morita-Baylis-Hillman Adducts Prepared from Eugenol, Thymol and Carvacrol
title_fullStr Synthesis and In Vitro Anti Leishmania amazonensis Biological Screening of Morita-Baylis-Hillman Adducts Prepared from Eugenol, Thymol and Carvacrol
title_full_unstemmed Synthesis and In Vitro Anti Leishmania amazonensis Biological Screening of Morita-Baylis-Hillman Adducts Prepared from Eugenol, Thymol and Carvacrol
title_short Synthesis and In Vitro Anti Leishmania amazonensis Biological Screening of Morita-Baylis-Hillman Adducts Prepared from Eugenol, Thymol and Carvacrol
title_sort synthesis and in vitro anti leishmania amazonensis biological screening of morita-baylis-hillman adducts prepared from eugenol, thymol and carvacrol
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274563/
https://www.ncbi.nlm.nih.gov/pubmed/27834831
http://dx.doi.org/10.3390/molecules21111483
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