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Synthesis of 5-(6-hydroxy-7H-purine-8-ylthio)- 2-(N-hydroxyformamido)pentanoic acid
We have developed a synthetic route for the preparation of a hybrid bisubstrate small molecule based on a nucleoside. A prototype compound was designed and docked into the catalytic domain of the AdSS enzyme bridging the region between the magnesium center of the protein to the nucleoside region. Th...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Beilstein-Institut
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2956464/ https://www.ncbi.nlm.nih.gov/pubmed/20978615 http://dx.doi.org/10.3762/bjoc.6.93 |
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author | Zhang, Yanmei Elliot, Greg Saldanha, Adrian Tsigelny, Igor Carson, Dennis Wrasidlo, Wolf |
author_facet | Zhang, Yanmei Elliot, Greg Saldanha, Adrian Tsigelny, Igor Carson, Dennis Wrasidlo, Wolf |
author_sort | Zhang, Yanmei |
collection | PubMed |
description | We have developed a synthetic route for the preparation of a hybrid bisubstrate small molecule based on a nucleoside. A prototype compound was designed and docked into the catalytic domain of the AdSS enzyme bridging the region between the magnesium center of the protein to the nucleoside region. The synthesis involves coupling a brominated peptide fragment capable of complexing magnesium to a thiolated nucleoside to obtain the hybrid model compound. |
format | Text |
id | pubmed-2956464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-29564642010-10-26 Synthesis of 5-(6-hydroxy-7H-purine-8-ylthio)- 2-(N-hydroxyformamido)pentanoic acid Zhang, Yanmei Elliot, Greg Saldanha, Adrian Tsigelny, Igor Carson, Dennis Wrasidlo, Wolf Beilstein J Org Chem Letter We have developed a synthetic route for the preparation of a hybrid bisubstrate small molecule based on a nucleoside. A prototype compound was designed and docked into the catalytic domain of the AdSS enzyme bridging the region between the magnesium center of the protein to the nucleoside region. The synthesis involves coupling a brominated peptide fragment capable of complexing magnesium to a thiolated nucleoside to obtain the hybrid model compound. Beilstein-Institut 2010-09-01 /pmc/articles/PMC2956464/ /pubmed/20978615 http://dx.doi.org/10.3762/bjoc.6.93 Text en Copyright © 2010, Zhang et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Letter Zhang, Yanmei Elliot, Greg Saldanha, Adrian Tsigelny, Igor Carson, Dennis Wrasidlo, Wolf Synthesis of 5-(6-hydroxy-7H-purine-8-ylthio)- 2-(N-hydroxyformamido)pentanoic acid |
title | Synthesis of 5-(6-hydroxy-7H-purine-8-ylthio)- 2-(N-hydroxyformamido)pentanoic acid |
title_full | Synthesis of 5-(6-hydroxy-7H-purine-8-ylthio)- 2-(N-hydroxyformamido)pentanoic acid |
title_fullStr | Synthesis of 5-(6-hydroxy-7H-purine-8-ylthio)- 2-(N-hydroxyformamido)pentanoic acid |
title_full_unstemmed | Synthesis of 5-(6-hydroxy-7H-purine-8-ylthio)- 2-(N-hydroxyformamido)pentanoic acid |
title_short | Synthesis of 5-(6-hydroxy-7H-purine-8-ylthio)- 2-(N-hydroxyformamido)pentanoic acid |
title_sort | synthesis of 5-(6-hydroxy-7h-purine-8-ylthio)- 2-(n-hydroxyformamido)pentanoic acid |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2956464/ https://www.ncbi.nlm.nih.gov/pubmed/20978615 http://dx.doi.org/10.3762/bjoc.6.93 |
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