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Gram-Scale Laboratory Synthesis of TC AC 28, a High-Affinity BET Bromodomain Ligand
[Image: see text] TC AC 28, 6-(1H-Indol-4-yl)-8-methoxy-1-methyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepine-4-acetic acid methyl ester, has been synthesized on a near-gram scale in seven steps with notable improvements in the reported poor-yielding last two steps enabling this key chemical probe c...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641879/ https://www.ncbi.nlm.nih.gov/pubmed/31457724 http://dx.doi.org/10.1021/acsomega.7b00780 |
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author | Khan, Raysa Marsh, Graham Felix, Robert Kemmitt, Paul D. Baud, Matthias G. J. Ciulli, Alessio Spencer, John |
author_facet | Khan, Raysa Marsh, Graham Felix, Robert Kemmitt, Paul D. Baud, Matthias G. J. Ciulli, Alessio Spencer, John |
author_sort | Khan, Raysa |
collection | PubMed |
description | [Image: see text] TC AC 28, 6-(1H-Indol-4-yl)-8-methoxy-1-methyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepine-4-acetic acid methyl ester, has been synthesized on a near-gram scale in seven steps with notable improvements in the reported poor-yielding last two steps enabling this key chemical probe compound to be available for researchers. |
format | Online Article Text |
id | pubmed-6641879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66418792019-08-27 Gram-Scale Laboratory Synthesis of TC AC 28, a High-Affinity BET Bromodomain Ligand Khan, Raysa Marsh, Graham Felix, Robert Kemmitt, Paul D. Baud, Matthias G. J. Ciulli, Alessio Spencer, John ACS Omega [Image: see text] TC AC 28, 6-(1H-Indol-4-yl)-8-methoxy-1-methyl-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepine-4-acetic acid methyl ester, has been synthesized on a near-gram scale in seven steps with notable improvements in the reported poor-yielding last two steps enabling this key chemical probe compound to be available for researchers. American Chemical Society 2017-08-08 /pmc/articles/PMC6641879/ /pubmed/31457724 http://dx.doi.org/10.1021/acsomega.7b00780 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Khan, Raysa Marsh, Graham Felix, Robert Kemmitt, Paul D. Baud, Matthias G. J. Ciulli, Alessio Spencer, John Gram-Scale Laboratory Synthesis of TC AC 28, a High-Affinity BET Bromodomain Ligand |
title | Gram-Scale Laboratory Synthesis of TC AC 28, a High-Affinity BET Bromodomain
Ligand |
title_full | Gram-Scale Laboratory Synthesis of TC AC 28, a High-Affinity BET Bromodomain
Ligand |
title_fullStr | Gram-Scale Laboratory Synthesis of TC AC 28, a High-Affinity BET Bromodomain
Ligand |
title_full_unstemmed | Gram-Scale Laboratory Synthesis of TC AC 28, a High-Affinity BET Bromodomain
Ligand |
title_short | Gram-Scale Laboratory Synthesis of TC AC 28, a High-Affinity BET Bromodomain
Ligand |
title_sort | gram-scale laboratory synthesis of tc ac 28, a high-affinity bet bromodomain
ligand |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641879/ https://www.ncbi.nlm.nih.gov/pubmed/31457724 http://dx.doi.org/10.1021/acsomega.7b00780 |
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