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Clostebol acetate
The title compound, C(21)H(29)ClO(3) [systematic name (8R,9S,10R,13S,14S,17S)-4-chloro-3-oxoandrost-4-en-17β-yl acetate], is a 4-chloro derivative of testosterone, used as an anabolic androgenic agent or applied topically in ophthalmological and dermatological treatments. The absolute configurations...
Autores principales: | , , , |
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Formato: | Online Artículo 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/PMC3212337/ https://www.ncbi.nlm.nih.gov/pubmed/22090994 http://dx.doi.org/10.1107/S1600536811026560 |
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author | Maccaroni, Elisabetta Mele, Andrea Del Rosso, Renato Malpezzi, Luciana |
author_facet | Maccaroni, Elisabetta Mele, Andrea Del Rosso, Renato Malpezzi, Luciana |
author_sort | Maccaroni, Elisabetta |
collection | PubMed |
description | The title compound, C(21)H(29)ClO(3) [systematic name (8R,9S,10R,13S,14S,17S)-4-chloro-3-oxoandrost-4-en-17β-yl acetate], is a 4-chloro derivative of testosterone, used as an anabolic androgenic agent or applied topically in ophthalmological and dermatological treatments. The absolute configurations at positions 8, 9, 10, 13, 14 and 17 were established by refinement of the Flack parameter as R, S, R, S, S, and S, respectively. Rings B and C of the steroid ring system adopt chair conformations, ring A has a half-chair conformation, while ring D is in a C(13) envelope conformation. Ring B and C, and C and D are trans fused. In the crystal, molecules are linked by a weak C—H⋯O interaction. |
format | Online Article Text |
id | pubmed-3212337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32123372011-11-16 Clostebol acetate Maccaroni, Elisabetta Mele, Andrea Del Rosso, Renato Malpezzi, Luciana Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(21)H(29)ClO(3) [systematic name (8R,9S,10R,13S,14S,17S)-4-chloro-3-oxoandrost-4-en-17β-yl acetate], is a 4-chloro derivative of testosterone, used as an anabolic androgenic agent or applied topically in ophthalmological and dermatological treatments. The absolute configurations at positions 8, 9, 10, 13, 14 and 17 were established by refinement of the Flack parameter as R, S, R, S, S, and S, respectively. Rings B and C of the steroid ring system adopt chair conformations, ring A has a half-chair conformation, while ring D is in a C(13) envelope conformation. Ring B and C, and C and D are trans fused. In the crystal, molecules are linked by a weak C—H⋯O interaction. International Union of Crystallography 2011-07-09 /pmc/articles/PMC3212337/ /pubmed/22090994 http://dx.doi.org/10.1107/S1600536811026560 Text en © Maccaroni 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 Maccaroni, Elisabetta Mele, Andrea Del Rosso, Renato Malpezzi, Luciana Clostebol acetate |
title | Clostebol acetate |
title_full | Clostebol acetate |
title_fullStr | Clostebol acetate |
title_full_unstemmed | Clostebol acetate |
title_short | Clostebol acetate |
title_sort | clostebol acetate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212337/ https://www.ncbi.nlm.nih.gov/pubmed/22090994 http://dx.doi.org/10.1107/S1600536811026560 |
work_keys_str_mv | AT maccaronielisabetta clostebolacetate AT meleandrea clostebolacetate AT delrossorenato clostebolacetate AT malpezziluciana clostebolacetate |