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Mesaconitine
The title compound, (1α,3α,6α,14α,15α,16β)-3,8,13,14,15-pentahydroxy-1,6,16-trimethoxy-4-methoxymethyl-20-methylaconitan-8,14-diyl 8-acetate 14-benzoate, C(33)H(45)NO(11), a C(19) diterpenoid alkaloid, obtained from the roots of Aconitum kusnezoffii, has been crystallographically characterized...
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961389/ https://www.ncbi.nlm.nih.gov/pubmed/21202557 http://dx.doi.org/10.1107/S1600536808013147 |
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author | He, Dao-Hang Zhu, Yong-Chuang Hu, Ai-Xi |
author_facet | He, Dao-Hang Zhu, Yong-Chuang Hu, Ai-Xi |
author_sort | He, Dao-Hang |
collection | PubMed |
description | The title compound, (1α,3α,6α,14α,15α,16β)-3,8,13,14,15-pentahydroxy-1,6,16-trimethoxy-4-methoxymethyl-20-methylaconitan-8,14-diyl 8-acetate 14-benzoate, C(33)H(45)NO(11), a C(19) diterpenoid alkaloid, obtained from the roots of Aconitum kusnezoffii, has been crystallographically characterized in this study. Rings A, B and E have chair conformations, rings C and F display envelope conformations, and ring D adopts a boat conformation. There are inter- and intramolecular O—H⋯O hydrogen bonds, the latter resulting in the formation of a non-planar seven-membered ring. The intermolecular interactions link the molecules into a two-dimensional network. |
format | Text |
id | pubmed-2961389 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29613892010-12-30 Mesaconitine He, Dao-Hang Zhu, Yong-Chuang Hu, Ai-Xi Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, (1α,3α,6α,14α,15α,16β)-3,8,13,14,15-pentahydroxy-1,6,16-trimethoxy-4-methoxymethyl-20-methylaconitan-8,14-diyl 8-acetate 14-benzoate, C(33)H(45)NO(11), a C(19) diterpenoid alkaloid, obtained from the roots of Aconitum kusnezoffii, has been crystallographically characterized in this study. Rings A, B and E have chair conformations, rings C and F display envelope conformations, and ring D adopts a boat conformation. There are inter- and intramolecular O—H⋯O hydrogen bonds, the latter resulting in the formation of a non-planar seven-membered ring. The intermolecular interactions link the molecules into a two-dimensional network. International Union of Crystallography 2008-05-10 /pmc/articles/PMC2961389/ /pubmed/21202557 http://dx.doi.org/10.1107/S1600536808013147 Text en © He 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 He, Dao-Hang Zhu, Yong-Chuang Hu, Ai-Xi Mesaconitine |
title | Mesaconitine |
title_full | Mesaconitine |
title_fullStr | Mesaconitine |
title_full_unstemmed | Mesaconitine |
title_short | Mesaconitine |
title_sort | mesaconitine |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961389/ https://www.ncbi.nlm.nih.gov/pubmed/21202557 http://dx.doi.org/10.1107/S1600536808013147 |
work_keys_str_mv | AT hedaohang mesaconitine AT zhuyongchuang mesaconitine AT huaixi mesaconitine |