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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...

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Autores principales: Maccaroni, Elisabetta, Mele, Andrea, Del Rosso, Renato, Malpezzi, Luciana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
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.
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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
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AT malpezziluciana clostebolacetate