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17β-Hydroxy-17α-methylandrosta-1,4-dien-3-one
The title compound, C(20)H(28)O(2), is a steroid with strong anabolic properties. The present solvent-free form crystallizes with two molecules per asymmetric unit. In the crystal, both molecules are involved in the formation of O—H⋯O hydrogen-bonded chains which extend along the b-axis direction....
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/PMC3588272/ https://www.ncbi.nlm.nih.gov/pubmed/23476441 http://dx.doi.org/10.1107/S1600536812049860 |
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author | Karpinska, Jolanta Erxleben, Andrea McArdle, Patrick |
author_facet | Karpinska, Jolanta Erxleben, Andrea McArdle, Patrick |
author_sort | Karpinska, Jolanta |
collection | PubMed |
description | The title compound, C(20)H(28)O(2), is a steroid with strong anabolic properties. The present solvent-free form crystallizes with two molecules per asymmetric unit. In the crystal, both molecules are involved in the formation of O—H⋯O hydrogen-bonded chains which extend along the b-axis direction. |
format | Online Article Text |
id | pubmed-3588272 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-35882722013-03-08 17β-Hydroxy-17α-methylandrosta-1,4-dien-3-one Karpinska, Jolanta Erxleben, Andrea McArdle, Patrick Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(20)H(28)O(2), is a steroid with strong anabolic properties. The present solvent-free form crystallizes with two molecules per asymmetric unit. In the crystal, both molecules are involved in the formation of O—H⋯O hydrogen-bonded chains which extend along the b-axis direction. International Union of Crystallography 2012-12-08 /pmc/articles/PMC3588272/ /pubmed/23476441 http://dx.doi.org/10.1107/S1600536812049860 Text en © Karpinska et al. 2013 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 Karpinska, Jolanta Erxleben, Andrea McArdle, Patrick 17β-Hydroxy-17α-methylandrosta-1,4-dien-3-one |
title | 17β-Hydroxy-17α-methylandrosta-1,4-dien-3-one |
title_full | 17β-Hydroxy-17α-methylandrosta-1,4-dien-3-one |
title_fullStr | 17β-Hydroxy-17α-methylandrosta-1,4-dien-3-one |
title_full_unstemmed | 17β-Hydroxy-17α-methylandrosta-1,4-dien-3-one |
title_short | 17β-Hydroxy-17α-methylandrosta-1,4-dien-3-one |
title_sort | 17β-hydroxy-17α-methylandrosta-1,4-dien-3-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588272/ https://www.ncbi.nlm.nih.gov/pubmed/23476441 http://dx.doi.org/10.1107/S1600536812049860 |
work_keys_str_mv | AT karpinskajolanta 17bhydroxy17amethylandrosta14dien3one AT erxlebenandrea 17bhydroxy17amethylandrosta14dien3one AT mcardlepatrick 17bhydroxy17amethylandrosta14dien3one |