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3α-Hydroxytirucalla-8,24-dien-21-oic acid
The title compound, C(30)H(48)O(3), a triterpene isolated from the resin of canarium schweinfurthiiand, is an isomer of the previously reported triterpene 3α-hydroxytirucalla-7,24-dien-21-oic acid [Mora et al. (2001 ▶). Acta Cryst. C57, 638–640], which crystallizes in the same trigonal space group...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3099970/ https://www.ncbi.nlm.nih.gov/pubmed/21754206 http://dx.doi.org/10.1107/S1600536811008956 |
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author | Yousuf, S. Kamdem, R. S. T. Ngadjui, B. T. Wafo, P. Fun, Hoong-Kun |
author_facet | Yousuf, S. Kamdem, R. S. T. Ngadjui, B. T. Wafo, P. Fun, Hoong-Kun |
author_sort | Yousuf, S. |
collection | PubMed |
description | The title compound, C(30)H(48)O(3), a triterpene isolated from the resin of canarium schweinfurthiiand, is an isomer of the previously reported triterpene 3α-hydroxytirucalla-7,24-dien-21-oic acid [Mora et al. (2001 ▶). Acta Cryst. C57, 638–640], which crystallizes in the same trigonal space group. The title molecule consists of four fused rings having chair, half-chair, half-chair and envelope conformations for rings A, B, C and D, respectively (steroid labelling). An intramolecular C—H⋯O hydrogen bond generates an S(7) ring. In the crystal, molecules are linked by O—H⋯O and C—H⋯O interactions, forming (001) sheets. |
format | Text |
id | pubmed-3099970 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30999702011-07-13 3α-Hydroxytirucalla-8,24-dien-21-oic acid Yousuf, S. Kamdem, R. S. T. Ngadjui, B. T. Wafo, P. Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(30)H(48)O(3), a triterpene isolated from the resin of canarium schweinfurthiiand, is an isomer of the previously reported triterpene 3α-hydroxytirucalla-7,24-dien-21-oic acid [Mora et al. (2001 ▶). Acta Cryst. C57, 638–640], which crystallizes in the same trigonal space group. The title molecule consists of four fused rings having chair, half-chair, half-chair and envelope conformations for rings A, B, C and D, respectively (steroid labelling). An intramolecular C—H⋯O hydrogen bond generates an S(7) ring. In the crystal, molecules are linked by O—H⋯O and C—H⋯O interactions, forming (001) sheets. International Union of Crystallography 2011-03-23 /pmc/articles/PMC3099970/ /pubmed/21754206 http://dx.doi.org/10.1107/S1600536811008956 Text en © Yousuf et al. 2011 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 Yousuf, S. Kamdem, R. S. T. Ngadjui, B. T. Wafo, P. Fun, Hoong-Kun 3α-Hydroxytirucalla-8,24-dien-21-oic acid |
title | 3α-Hydroxytirucalla-8,24-dien-21-oic acid |
title_full | 3α-Hydroxytirucalla-8,24-dien-21-oic acid |
title_fullStr | 3α-Hydroxytirucalla-8,24-dien-21-oic acid |
title_full_unstemmed | 3α-Hydroxytirucalla-8,24-dien-21-oic acid |
title_short | 3α-Hydroxytirucalla-8,24-dien-21-oic acid |
title_sort | 3α-hydroxytirucalla-8,24-dien-21-oic acid |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3099970/ https://www.ncbi.nlm.nih.gov/pubmed/21754206 http://dx.doi.org/10.1107/S1600536811008956 |
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