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Identification of (−)(E)-N-[2(S)-Hydroxy-2-(4-hydroxyphenyl) ethyl]ferulamide, a Natural Product Isolated from Croton Pullei: Theoretical and Experimental Analysis

Ferulic acid (FA) and its derivatives (FADs) are known for a variety of biological activities, such as photo-protective agent, antioxidant, antiatherogenic and antiplasmodial activities. During structural definition of a FAD isolated from Croton pullei, the possibility of a heterologous series made...

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Autores principales: Silva, Silvana de O., Peixoto, Rosana N.S., Silva, José Rogério A., Alves, Cláudio N., Guilhon, Giselle M.S.P., Santos, Lourivaldo S., Brasil, Davi do S.B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3257136/
https://www.ncbi.nlm.nih.gov/pubmed/22272139
http://dx.doi.org/10.3390/ijms12129389
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author Silva, Silvana de O.
Peixoto, Rosana N.S.
Silva, José Rogério A.
Alves, Cláudio N.
Guilhon, Giselle M.S.P.
Santos, Lourivaldo S.
Brasil, Davi do S.B.
author_facet Silva, Silvana de O.
Peixoto, Rosana N.S.
Silva, José Rogério A.
Alves, Cláudio N.
Guilhon, Giselle M.S.P.
Santos, Lourivaldo S.
Brasil, Davi do S.B.
author_sort Silva, Silvana de O.
collection PubMed
description Ferulic acid (FA) and its derivatives (FADs) are known for a variety of biological activities, such as photo-protective agent, antioxidant, antiatherogenic and antiplasmodial activities. During structural definition of a FAD isolated from Croton pullei, the possibility of a heterologous series made this definition difficult. In this regard, computational simulations were performed using theoretical calculations at DFT level to predict Infrared (IR) and Nuclear Magnetic Resonance (NMR) data. The IR and NMR (13)C and (1)H data were compared with the theoretical calculations performed for three structural possibilities of a heterologous series. The theoretical results were compared with the experimental data through linear regression in order to define the most probable structure and showed satisfactory values.
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spelling pubmed-32571362012-01-23 Identification of (−)(E)-N-[2(S)-Hydroxy-2-(4-hydroxyphenyl) ethyl]ferulamide, a Natural Product Isolated from Croton Pullei: Theoretical and Experimental Analysis Silva, Silvana de O. Peixoto, Rosana N.S. Silva, José Rogério A. Alves, Cláudio N. Guilhon, Giselle M.S.P. Santos, Lourivaldo S. Brasil, Davi do S.B. Int J Mol Sci Article Ferulic acid (FA) and its derivatives (FADs) are known for a variety of biological activities, such as photo-protective agent, antioxidant, antiatherogenic and antiplasmodial activities. During structural definition of a FAD isolated from Croton pullei, the possibility of a heterologous series made this definition difficult. In this regard, computational simulations were performed using theoretical calculations at DFT level to predict Infrared (IR) and Nuclear Magnetic Resonance (NMR) data. The IR and NMR (13)C and (1)H data were compared with the theoretical calculations performed for three structural possibilities of a heterologous series. The theoretical results were compared with the experimental data through linear regression in order to define the most probable structure and showed satisfactory values. Molecular Diversity Preservation International (MDPI) 2011-12-15 /pmc/articles/PMC3257136/ /pubmed/22272139 http://dx.doi.org/10.3390/ijms12129389 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Silva, Silvana de O.
Peixoto, Rosana N.S.
Silva, José Rogério A.
Alves, Cláudio N.
Guilhon, Giselle M.S.P.
Santos, Lourivaldo S.
Brasil, Davi do S.B.
Identification of (−)(E)-N-[2(S)-Hydroxy-2-(4-hydroxyphenyl) ethyl]ferulamide, a Natural Product Isolated from Croton Pullei: Theoretical and Experimental Analysis
title Identification of (−)(E)-N-[2(S)-Hydroxy-2-(4-hydroxyphenyl) ethyl]ferulamide, a Natural Product Isolated from Croton Pullei: Theoretical and Experimental Analysis
title_full Identification of (−)(E)-N-[2(S)-Hydroxy-2-(4-hydroxyphenyl) ethyl]ferulamide, a Natural Product Isolated from Croton Pullei: Theoretical and Experimental Analysis
title_fullStr Identification of (−)(E)-N-[2(S)-Hydroxy-2-(4-hydroxyphenyl) ethyl]ferulamide, a Natural Product Isolated from Croton Pullei: Theoretical and Experimental Analysis
title_full_unstemmed Identification of (−)(E)-N-[2(S)-Hydroxy-2-(4-hydroxyphenyl) ethyl]ferulamide, a Natural Product Isolated from Croton Pullei: Theoretical and Experimental Analysis
title_short Identification of (−)(E)-N-[2(S)-Hydroxy-2-(4-hydroxyphenyl) ethyl]ferulamide, a Natural Product Isolated from Croton Pullei: Theoretical and Experimental Analysis
title_sort identification of (−)(e)-n-[2(s)-hydroxy-2-(4-hydroxyphenyl) ethyl]ferulamide, a natural product isolated from croton pullei: theoretical and experimental analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3257136/
https://www.ncbi.nlm.nih.gov/pubmed/22272139
http://dx.doi.org/10.3390/ijms12129389
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