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l-2-Nitrimino-1,3-diazepane-4-carboxylic acid
The cyclic form of l-nitroarginine, C(6)H(10)N(4)O(4), crystallizes with two independent molecules in the asymmetric unit. According to the geometrical parameters, similar in both molecules, the structure corresponds to that of l-2-nitrimino-1,3-diazepane-4-carboxylic acid; there are, however, co...
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961324/ https://www.ncbi.nlm.nih.gov/pubmed/21202424 http://dx.doi.org/10.1107/S1600536808011835 |
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author | Karapetyan, Harutyun A. |
author_facet | Karapetyan, Harutyun A. |
author_sort | Karapetyan, Harutyun A. |
collection | PubMed |
description | The cyclic form of l-nitroarginine, C(6)H(10)N(4)O(4), crystallizes with two independent molecules in the asymmetric unit. According to the geometrical parameters, similar in both molecules, the structure corresponds to that of l-2-nitrimino-1,3-diazepane-4-carboxylic acid; there are, however, conformational differences between the independent molecules, one of them being close to a twisted chair while the other might be described as a rather flattened boat. All six active H atoms in the two molecules are involved in hydrogen bonds, two of which are intramolecular and four intermolecular, forming an infinite chain of molecules along the b axis. |
format | Text |
id | pubmed-2961324 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29613242010-12-30 l-2-Nitrimino-1,3-diazepane-4-carboxylic acid Karapetyan, Harutyun A. Acta Crystallogr Sect E Struct Rep Online Organic Papers The cyclic form of l-nitroarginine, C(6)H(10)N(4)O(4), crystallizes with two independent molecules in the asymmetric unit. According to the geometrical parameters, similar in both molecules, the structure corresponds to that of l-2-nitrimino-1,3-diazepane-4-carboxylic acid; there are, however, conformational differences between the independent molecules, one of them being close to a twisted chair while the other might be described as a rather flattened boat. All six active H atoms in the two molecules are involved in hydrogen bonds, two of which are intramolecular and four intermolecular, forming an infinite chain of molecules along the b axis. International Union of Crystallography 2008-04-30 /pmc/articles/PMC2961324/ /pubmed/21202424 http://dx.doi.org/10.1107/S1600536808011835 Text en © Harutyun A. Karapetyan 2008 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 Karapetyan, Harutyun A. l-2-Nitrimino-1,3-diazepane-4-carboxylic acid |
title |
l-2-Nitrimino-1,3-diazepane-4-carboxylic acid |
title_full |
l-2-Nitrimino-1,3-diazepane-4-carboxylic acid |
title_fullStr |
l-2-Nitrimino-1,3-diazepane-4-carboxylic acid |
title_full_unstemmed |
l-2-Nitrimino-1,3-diazepane-4-carboxylic acid |
title_short |
l-2-Nitrimino-1,3-diazepane-4-carboxylic acid |
title_sort | l-2-nitrimino-1,3-diazepane-4-carboxylic acid |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961324/ https://www.ncbi.nlm.nih.gov/pubmed/21202424 http://dx.doi.org/10.1107/S1600536808011835 |
work_keys_str_mv | AT karapetyanharutyuna l2nitrimino13diazepane4carboxylicacid |