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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2016
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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. |
format | Online Article Text |
id | pubmed-6274563 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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