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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...

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Autores principales: Uzzaman, Shams, Khanam, Hena, Mashrai, Ashraf, Mabkhot, Yahia Nasser, Husain, Ahmad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
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].
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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
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