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6-Hydroxyimino-5α-cholestane
The title compound, C(27)H(47)NO, is a steroid derivative composed of a saturated carbon fused-ring framework with an alkyl side chain. Ring bond lengths have normal values with an average of 1.533 (2) Å, while the cholestane side chain shows an average bond length of 1.533 (2) Å. The three cyclohex...
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/PMC3470390/ https://www.ncbi.nlm.nih.gov/pubmed/23125803 http://dx.doi.org/10.1107/S1600536812040093 |
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author | Uzzaman, Shams Khanam, Hena Mashrai, Ashraf Mabkhot, Yahia Nasser Husain, Ahmad |
author_facet | Uzzaman, Shams Khanam, Hena Mashrai, Ashraf Mabkhot, Yahia Nasser Husain, Ahmad |
author_sort | Uzzaman, Shams |
collection | PubMed |
description | The title compound, C(27)H(47)NO, is a steroid derivative composed of a saturated carbon fused-ring framework with an alkyl side chain. Ring bond lengths have normal values with an average of 1.533 (2) Å, while the cholestane side chain shows an average bond length of 1.533 (2) Å. The three cyclohexane rings adopt chair conformations or close to chair conformations while the cyclopentane ring is twisted. The cholesterol side-chain is fully extended with a gauche–trans conformation of the terminal methyl groups. There are eight chiral centres in the molecule; the absolute configuration of these sites was determined from the structure presented. There are two molecules in the asymmetric unit; in one, the alkyl chain is disordered over two sets of sites [occupancy ratios of 0.50:0.50 and 0.67:0.33]. |
format | Online Article Text |
id | pubmed-3470390 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-34703902012-11-02 6-Hydroxyimino-5α-cholestane Uzzaman, Shams Khanam, Hena Mashrai, Ashraf Mabkhot, Yahia Nasser Husain, Ahmad Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(27)H(47)NO, is a steroid derivative composed of a saturated carbon fused-ring framework with an alkyl side chain. Ring bond lengths have normal values with an average of 1.533 (2) Å, while the cholestane side chain shows an average bond length of 1.533 (2) Å. The three cyclohexane rings adopt chair conformations or close to chair conformations while the cyclopentane ring is twisted. The cholesterol side-chain is fully extended with a gauche–trans conformation of the terminal methyl groups. There are eight chiral centres in the molecule; the absolute configuration of these sites was determined from the structure presented. There are two molecules in the asymmetric unit; in one, the alkyl chain is disordered over two sets of sites [occupancy ratios of 0.50:0.50 and 0.67:0.33]. International Union of Crystallography 2012-09-29 /pmc/articles/PMC3470390/ /pubmed/23125803 http://dx.doi.org/10.1107/S1600536812040093 Text en © Uzzaman 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 Uzzaman, Shams Khanam, Hena Mashrai, Ashraf Mabkhot, Yahia Nasser Husain, Ahmad 6-Hydroxyimino-5α-cholestane |
title | 6-Hydroxyimino-5α-cholestane |
title_full | 6-Hydroxyimino-5α-cholestane |
title_fullStr | 6-Hydroxyimino-5α-cholestane |
title_full_unstemmed | 6-Hydroxyimino-5α-cholestane |
title_short | 6-Hydroxyimino-5α-cholestane |
title_sort | 6-hydroxyimino-5α-cholestane |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3470390/ https://www.ncbi.nlm.nih.gov/pubmed/23125803 http://dx.doi.org/10.1107/S1600536812040093 |
work_keys_str_mv | AT uzzamanshams 6hydroxyimino5acholestane AT khanamhena 6hydroxyimino5acholestane AT mashraiashraf 6hydroxyimino5acholestane AT mabkhotyahianasser 6hydroxyimino5acholestane AT husainahmad 6hydroxyimino5acholestane |