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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
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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. |
format | Online Article Text |
id | pubmed-3247358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT wangcheng thailandepsina AT chengyiqiang thailandepsina |