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Thailandepsin A

Thailandepsin A [systematic name: (E)-(1S,5S,6R,9S,20R)-6-[(2S)-butan-2-yl]-5-hy­droxy-20-[2-(meth­yl­sulfan­yl)eth­yl]-2-oxa-11,12-dithia-7,19,22-triaza­bicyclo­[7.7.6]docosa-15-ene-3,8,18,21-tetra­one], C(23)H(37)N(3)O(6)S(3), is a newly reported [Wang et al. (2011). J. Nat. Prod. doi:10.1021/np20...

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Detalles Bibliográficos
Autores principales: Wang, Cheng, Cheng, Yi-Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247358/
https://www.ncbi.nlm.nih.gov/pubmed/22219976
http://dx.doi.org/10.1107/S1600536811041390
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author Wang, Cheng
Cheng, Yi-Qiang
author_facet Wang, Cheng
Cheng, Yi-Qiang
author_sort Wang, Cheng
collection PubMed
description Thailandepsin A [systematic name: (E)-(1S,5S,6R,9S,20R)-6-[(2S)-butan-2-yl]-5-hy­droxy-20-[2-(meth­yl­sulfan­yl)eth­yl]-2-oxa-11,12-dithia-7,19,22-triaza­bicyclo­[7.7.6]docosa-15-ene-3,8,18,21-tetra­one], C(23)H(37)N(3)O(6)S(3), is a newly reported [Wang et al. (2011). J. Nat. Prod. doi:10.1021/np200324x] bicyclic depsipeptide that has potent histone deacetyl­ase inhibitory activity and broad-spectrum anti­proliferative activity. The absolute configuration of thailandepsin A has been determined from the anomalous dispersion and the stereochemistry of all chiral C atoms. Intra­molecular N—H⋯O and N—H⋯S hydrogen bonds occur. Inter­molecular N—H⋯O and O—H⋯O hydrogen bonds are observed in the crystal structure.
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spelling pubmed-32473582012-01-04 Thailandepsin A Wang, Cheng Cheng, Yi-Qiang Acta Crystallogr Sect E Struct Rep Online Organic Papers Thailandepsin A [systematic name: (E)-(1S,5S,6R,9S,20R)-6-[(2S)-butan-2-yl]-5-hy­droxy-20-[2-(meth­yl­sulfan­yl)eth­yl]-2-oxa-11,12-dithia-7,19,22-triaza­bicyclo­[7.7.6]docosa-15-ene-3,8,18,21-tetra­one], C(23)H(37)N(3)O(6)S(3), is a newly reported [Wang et al. (2011). J. Nat. Prod. doi:10.1021/np200324x] bicyclic depsipeptide that has potent histone deacetyl­ase inhibitory activity and broad-spectrum anti­proliferative activity. The absolute configuration of thailandepsin A has been determined from the anomalous dispersion and the stereochemistry of all chiral C atoms. Intra­molecular N—H⋯O and N—H⋯S hydrogen bonds occur. Inter­molecular N—H⋯O and O—H⋯O hydrogen bonds are observed in the crystal structure. International Union of Crystallography 2011-10-12 /pmc/articles/PMC3247358/ /pubmed/22219976 http://dx.doi.org/10.1107/S1600536811041390 Text en © Wang and Cheng 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
Wang, Cheng
Cheng, Yi-Qiang
Thailandepsin A
title Thailandepsin A
title_full Thailandepsin A
title_fullStr Thailandepsin A
title_full_unstemmed Thailandepsin A
title_short Thailandepsin A
title_sort thailandepsin a
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247358/
https://www.ncbi.nlm.nih.gov/pubmed/22219976
http://dx.doi.org/10.1107/S1600536811041390
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