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Hoodigogenin A from Hoodia gordonii
The title molecule (systematic name: 12-O-β-tigloyl-3β,14β-dihydroxypregn-5-en-20-one), C(26)H(38)O(5), isolated from aerial parts of Hoodia gordonii, has its steroid A and C rings in chair conformations, its B ring in a half-chair conformation, and its five-membered ring in an envelope conformati...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962224/ https://www.ncbi.nlm.nih.gov/pubmed/21203331 http://dx.doi.org/10.1107/S1600536808022368 |
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author | Shukla, Yatin J. Fronczek, Frank R. Pawar, Rahul S. Khan, Ikhlas A. |
author_facet | Shukla, Yatin J. Fronczek, Frank R. Pawar, Rahul S. Khan, Ikhlas A. |
author_sort | Shukla, Yatin J. |
collection | PubMed |
description | The title molecule (systematic name: 12-O-β-tigloyl-3β,14β-dihydroxypregn-5-en-20-one), C(26)H(38)O(5), isolated from aerial parts of Hoodia gordonii, has its steroid A and C rings in chair conformations, its B ring in a half-chair conformation, and its five-membered ring in an envelope conformation. The OH group at the C/D ring junction forms an intramolecular hydrogen bond with the keto substituent. The OH group on the A ring forms an intermolecular hydrogen bond with the tiglate C=O group, propagating [010] chains in the crystal structure. |
format | Text |
id | pubmed-2962224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29622242010-12-30 Hoodigogenin A from Hoodia gordonii Shukla, Yatin J. Fronczek, Frank R. Pawar, Rahul S. Khan, Ikhlas A. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title molecule (systematic name: 12-O-β-tigloyl-3β,14β-dihydroxypregn-5-en-20-one), C(26)H(38)O(5), isolated from aerial parts of Hoodia gordonii, has its steroid A and C rings in chair conformations, its B ring in a half-chair conformation, and its five-membered ring in an envelope conformation. The OH group at the C/D ring junction forms an intramolecular hydrogen bond with the keto substituent. The OH group on the A ring forms an intermolecular hydrogen bond with the tiglate C=O group, propagating [010] chains in the crystal structure. International Union of Crystallography 2008-07-31 /pmc/articles/PMC2962224/ /pubmed/21203331 http://dx.doi.org/10.1107/S1600536808022368 Text en © Shukla et al. 2008 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 Shukla, Yatin J. Fronczek, Frank R. Pawar, Rahul S. Khan, Ikhlas A. Hoodigogenin A from Hoodia gordonii |
title | Hoodigogenin A from Hoodia gordonii
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title_full | Hoodigogenin A from Hoodia gordonii
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title_fullStr | Hoodigogenin A from Hoodia gordonii
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title_full_unstemmed | Hoodigogenin A from Hoodia gordonii
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title_short | Hoodigogenin A from Hoodia gordonii
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title_sort | hoodigogenin a from hoodia gordonii |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962224/ https://www.ncbi.nlm.nih.gov/pubmed/21203331 http://dx.doi.org/10.1107/S1600536808022368 |
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