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(10E,12E,14E)-9,16-Dioxooctadeca-10,12,14-trienoic acid
The title octadecatrienoic acid derivative, C(18)H(26)O(4), was isolated from Silene maritima With. (Caryophyllaceae), the first time this natural compound has been found in the Caryophyllales order. This fatty acid has an 18-carbon backbone with three double bonds on trans (E) conformation and tw...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3435652/ https://www.ncbi.nlm.nih.gov/pubmed/22969525 http://dx.doi.org/10.1107/S1600536812027870 |
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author | Bréant, Lise Vonthron-Sénécheau, Catherine Brelot, Lydia Lobstein, Annelise |
author_facet | Bréant, Lise Vonthron-Sénécheau, Catherine Brelot, Lydia Lobstein, Annelise |
author_sort | Bréant, Lise |
collection | PubMed |
description | The title octadecatrienoic acid derivative, C(18)H(26)O(4), was isolated from Silene maritima With. (Caryophyllaceae), the first time this natural compound has been found in the Caryophyllales order. This fatty acid has an 18-carbon backbone with three double bonds on trans (E) conformation and two carbonyl. In the crystal, molecules are linked via pairs of O—H⋯O hydrogen bonds, forming inversion dimers. |
format | Online Article Text |
id | pubmed-3435652 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-34356522012-09-11 (10E,12E,14E)-9,16-Dioxooctadeca-10,12,14-trienoic acid Bréant, Lise Vonthron-Sénécheau, Catherine Brelot, Lydia Lobstein, Annelise Acta Crystallogr Sect E Struct Rep Online Organic Papers The title octadecatrienoic acid derivative, C(18)H(26)O(4), was isolated from Silene maritima With. (Caryophyllaceae), the first time this natural compound has been found in the Caryophyllales order. This fatty acid has an 18-carbon backbone with three double bonds on trans (E) conformation and two carbonyl. In the crystal, molecules are linked via pairs of O—H⋯O hydrogen bonds, forming inversion dimers. International Union of Crystallography 2012-08-01 /pmc/articles/PMC3435652/ /pubmed/22969525 http://dx.doi.org/10.1107/S1600536812027870 Text en © Bréant et al. 2012 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 Bréant, Lise Vonthron-Sénécheau, Catherine Brelot, Lydia Lobstein, Annelise (10E,12E,14E)-9,16-Dioxooctadeca-10,12,14-trienoic acid |
title | (10E,12E,14E)-9,16-Dioxooctadeca-10,12,14-trienoic acid |
title_full | (10E,12E,14E)-9,16-Dioxooctadeca-10,12,14-trienoic acid |
title_fullStr | (10E,12E,14E)-9,16-Dioxooctadeca-10,12,14-trienoic acid |
title_full_unstemmed | (10E,12E,14E)-9,16-Dioxooctadeca-10,12,14-trienoic acid |
title_short | (10E,12E,14E)-9,16-Dioxooctadeca-10,12,14-trienoic acid |
title_sort | (10e,12e,14e)-9,16-dioxooctadeca-10,12,14-trienoic acid |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3435652/ https://www.ncbi.nlm.nih.gov/pubmed/22969525 http://dx.doi.org/10.1107/S1600536812027870 |
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