(22E,24R)-3β,5α,9α-Trihy­droxy­ergosta-7,22-dien-6-one monohydrate

The title ergosterol compound, C(28)H(44)O(4)·H(2)O, is composed of four fused rings (three six-membered and one five-membered) and a side chain. It is a derivative of ergosterol and was isolated from a marine-derived halotolerant fungus, Cladosporium cladosporioides PXP-49. In the crystal, mol­ecul...

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Detalles Bibliográficos
Autores principales: Xu, Zhi-Hong, Peng, Xiao-Ping, Wang, Yi, Zhu, Wei-Ming
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089332/
https://www.ncbi.nlm.nih.gov/pubmed/21754450
http://dx.doi.org/10.1107/S160053681101347X
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author Xu, Zhi-Hong
Peng, Xiao-Ping
Wang, Yi
Zhu, Wei-Ming
author_facet Xu, Zhi-Hong
Peng, Xiao-Ping
Wang, Yi
Zhu, Wei-Ming
author_sort Xu, Zhi-Hong
collection PubMed
description The title ergosterol compound, C(28)H(44)O(4)·H(2)O, is composed of four fused rings (three six-membered and one five-membered) and a side chain. It is a derivative of ergosterol and was isolated from a marine-derived halotolerant fungus, Cladosporium cladosporioides PXP-49. In the crystal, mol­ecules are assembled by classical O—H⋯O hydrogen bonds, forming a two-dimensional network, with base vectors [100] and [010]. The absolute configuration was assigned from the measured optical rotation and reference to the literature. An intra­molecular O—H⋯O hydrogen bond occurs.
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spelling pubmed-30893322011-07-13 (22E,24R)-3β,5α,9α-Trihy­droxy­ergosta-7,22-dien-6-one monohydrate Xu, Zhi-Hong Peng, Xiao-Ping Wang, Yi Zhu, Wei-Ming Acta Crystallogr Sect E Struct Rep Online Organic Papers The title ergosterol compound, C(28)H(44)O(4)·H(2)O, is composed of four fused rings (three six-membered and one five-membered) and a side chain. It is a derivative of ergosterol and was isolated from a marine-derived halotolerant fungus, Cladosporium cladosporioides PXP-49. In the crystal, mol­ecules are assembled by classical O—H⋯O hydrogen bonds, forming a two-dimensional network, with base vectors [100] and [010]. The absolute configuration was assigned from the measured optical rotation and reference to the literature. An intra­molecular O—H⋯O hydrogen bond occurs. International Union of Crystallography 2011-04-16 /pmc/articles/PMC3089332/ /pubmed/21754450 http://dx.doi.org/10.1107/S160053681101347X Text en © Xu 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
Xu, Zhi-Hong
Peng, Xiao-Ping
Wang, Yi
Zhu, Wei-Ming
(22E,24R)-3β,5α,9α-Trihy­droxy­ergosta-7,22-dien-6-one monohydrate
title (22E,24R)-3β,5α,9α-Trihy­droxy­ergosta-7,22-dien-6-one monohydrate
title_full (22E,24R)-3β,5α,9α-Trihy­droxy­ergosta-7,22-dien-6-one monohydrate
title_fullStr (22E,24R)-3β,5α,9α-Trihy­droxy­ergosta-7,22-dien-6-one monohydrate
title_full_unstemmed (22E,24R)-3β,5α,9α-Trihy­droxy­ergosta-7,22-dien-6-one monohydrate
title_short (22E,24R)-3β,5α,9α-Trihy­droxy­ergosta-7,22-dien-6-one monohydrate
title_sort (22e,24r)-3β,5α,9α-trihy­droxy­ergosta-7,22-dien-6-one monohydrate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089332/
https://www.ncbi.nlm.nih.gov/pubmed/21754450
http://dx.doi.org/10.1107/S160053681101347X
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