N-(β-Carb­oxy­eth­yl)-α-isoleucine

The title compound, {2-[(2-carbamoyleth­yl)amino]-3-methyl­penta­noic acid}, C(9)H(18)N(2)O(3), is of inter­est with respect to its biological activity. It was formed during an addition reaction between acryl­amide and the amino acid isoleucine. The crystal structure is a three-dimensional network b...

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Detalles Bibliográficos
Autores principales: Nehls, Irene, Hanebeck, Olaf, Becker, Roland, Emmerling, Franziska
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569235/
https://www.ncbi.nlm.nih.gov/pubmed/23424458
http://dx.doi.org/10.1107/S160053681205146X
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author Nehls, Irene
Hanebeck, Olaf
Becker, Roland
Emmerling, Franziska
author_facet Nehls, Irene
Hanebeck, Olaf
Becker, Roland
Emmerling, Franziska
author_sort Nehls, Irene
collection PubMed
description The title compound, {2-[(2-carbamoyleth­yl)amino]-3-methyl­penta­noic acid}, C(9)H(18)N(2)O(3), is of inter­est with respect to its biological activity. It was formed during an addition reaction between acryl­amide and the amino acid isoleucine. The crystal structure is a three-dimensional network built up by inter­molecular N—H⋯O and O—H⋯N hydrogen bonds.
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spelling pubmed-35692352013-02-19 N-(β-Carb­oxy­eth­yl)-α-isoleucine Nehls, Irene Hanebeck, Olaf Becker, Roland Emmerling, Franziska Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, {2-[(2-carbamoyleth­yl)amino]-3-methyl­penta­noic acid}, C(9)H(18)N(2)O(3), is of inter­est with respect to its biological activity. It was formed during an addition reaction between acryl­amide and the amino acid isoleucine. The crystal structure is a three-dimensional network built up by inter­molecular N—H⋯O and O—H⋯N hydrogen bonds. International Union of Crystallography 2013-01-04 /pmc/articles/PMC3569235/ /pubmed/23424458 http://dx.doi.org/10.1107/S160053681205146X Text en © Nehls et al. 2013 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Nehls, Irene
Hanebeck, Olaf
Becker, Roland
Emmerling, Franziska
N-(β-Carb­oxy­eth­yl)-α-isoleucine
title N-(β-Carb­oxy­eth­yl)-α-isoleucine
title_full N-(β-Carb­oxy­eth­yl)-α-isoleucine
title_fullStr N-(β-Carb­oxy­eth­yl)-α-isoleucine
title_full_unstemmed N-(β-Carb­oxy­eth­yl)-α-isoleucine
title_short N-(β-Carb­oxy­eth­yl)-α-isoleucine
title_sort n-(β-carb­oxy­eth­yl)-α-isoleucine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569235/
https://www.ncbi.nlm.nih.gov/pubmed/23424458
http://dx.doi.org/10.1107/S160053681205146X
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AT hanebeckolaf nbcarboxyethylaisoleucine
AT beckerroland nbcarboxyethylaisoleucine
AT emmerlingfranziska nbcarboxyethylaisoleucine

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