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17α-Acetoxy-11β-hydroxy-6α-methylpregn-4-ene-3,20-dione
The title compound, C(24)H(34)O(5), a fungal-transformed metabolite of the injectable contraceptive medroxyprogesterone acetate, consists of four fused rings (A, B, C and D; steroid labelling). Ring A exists in a half-chair conformation while trans-fused rings B and C adopt chair conformations. The...
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/PMC3393278/ https://www.ncbi.nlm.nih.gov/pubmed/22807835 http://dx.doi.org/10.1107/S1600536812017631 |
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author | Yousuf, Sammer Bano, Saira Choudhary, M. Iqbal |
author_facet | Yousuf, Sammer Bano, Saira Choudhary, M. Iqbal |
author_sort | Yousuf, Sammer |
collection | PubMed |
description | The title compound, C(24)H(34)O(5), a fungal-transformed metabolite of the injectable contraceptive medroxyprogesterone acetate, consists of four fused rings (A, B, C and D; steroid labelling). Ring A exists in a half-chair conformation while trans-fused rings B and C adopt chair conformations. The five-membered ring D adopts an envelope conformation with the C atom bound to the methyl group at the flap. In the crystal, adjacent molecules are linked by O—H⋯O and C—H⋯O hydrogen bonds, forming infinite chains along the a axis. |
format | Online Article Text |
id | pubmed-3393278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-33932782012-07-17 17α-Acetoxy-11β-hydroxy-6α-methylpregn-4-ene-3,20-dione Yousuf, Sammer Bano, Saira Choudhary, M. Iqbal Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(24)H(34)O(5), a fungal-transformed metabolite of the injectable contraceptive medroxyprogesterone acetate, consists of four fused rings (A, B, C and D; steroid labelling). Ring A exists in a half-chair conformation while trans-fused rings B and C adopt chair conformations. The five-membered ring D adopts an envelope conformation with the C atom bound to the methyl group at the flap. In the crystal, adjacent molecules are linked by O—H⋯O and C—H⋯O hydrogen bonds, forming infinite chains along the a axis. International Union of Crystallography 2012-06-13 /pmc/articles/PMC3393278/ /pubmed/22807835 http://dx.doi.org/10.1107/S1600536812017631 Text en © Yousuf 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 Yousuf, Sammer Bano, Saira Choudhary, M. Iqbal 17α-Acetoxy-11β-hydroxy-6α-methylpregn-4-ene-3,20-dione |
title | 17α-Acetoxy-11β-hydroxy-6α-methylpregn-4-ene-3,20-dione |
title_full | 17α-Acetoxy-11β-hydroxy-6α-methylpregn-4-ene-3,20-dione |
title_fullStr | 17α-Acetoxy-11β-hydroxy-6α-methylpregn-4-ene-3,20-dione |
title_full_unstemmed | 17α-Acetoxy-11β-hydroxy-6α-methylpregn-4-ene-3,20-dione |
title_short | 17α-Acetoxy-11β-hydroxy-6α-methylpregn-4-ene-3,20-dione |
title_sort | 17α-acetoxy-11β-hydroxy-6α-methylpregn-4-ene-3,20-dione |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393278/ https://www.ncbi.nlm.nih.gov/pubmed/22807835 http://dx.doi.org/10.1107/S1600536812017631 |
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