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Synthesis and characterisation of 5-acyl-6,7-dihydrothieno[3,2-c]pyridine inhibitors of Hedgehog acyltransferase
In this data article we describe synthetic and characterisation data for four members of the 5-acyl-6,7-dihydrothieno[3,2-c]pyridine (termed “RU-SKI”) class of inhibitors of Hedgehog acyltransferase, including associated NMR spectra for final compounds. RU-SKI compounds were selected for synthesis b...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816282/ https://www.ncbi.nlm.nih.gov/pubmed/27077078 http://dx.doi.org/10.1016/j.dib.2016.02.012 |
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author | Lanyon-Hogg, Thomas Masumoto, Naoko Bodakh, George Konitsiotis, Antonio D. Thinon, Emmanuelle Rodgers, Ursula R. Owens, Raymond J. Magee, Anthony I. Tate, Edward W. |
author_facet | Lanyon-Hogg, Thomas Masumoto, Naoko Bodakh, George Konitsiotis, Antonio D. Thinon, Emmanuelle Rodgers, Ursula R. Owens, Raymond J. Magee, Anthony I. Tate, Edward W. |
author_sort | Lanyon-Hogg, Thomas |
collection | PubMed |
description | In this data article we describe synthetic and characterisation data for four members of the 5-acyl-6,7-dihydrothieno[3,2-c]pyridine (termed “RU-SKI”) class of inhibitors of Hedgehog acyltransferase, including associated NMR spectra for final compounds. RU-SKI compounds were selected for synthesis based on their published high potencies against the enzyme target. RU-SKI 41 (9a), RU-SKI 43 (9b), RU-SKI 101 (9c), and RU-SKI 201 (9d) were profiled for activity in the related article “Click chemistry armed enzyme linked immunosorbent assay to measure palmitoylation by Hedgehog acyltransferase” (Lanyon-Hogg et al., 2015) [1]. (1)H NMR spectral data indicate different amide conformational ratios between the RU-SKI inhibitors, as has been observed in other 5-acyl-6,7-dihydrothieno[3,2-c]pyridines. The synthetic and characterisation data supplied in the current article provide validated access to the class of RU-SKI inhibitors. |
format | Online Article Text |
id | pubmed-4816282 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-48162822016-04-13 Synthesis and characterisation of 5-acyl-6,7-dihydrothieno[3,2-c]pyridine inhibitors of Hedgehog acyltransferase Lanyon-Hogg, Thomas Masumoto, Naoko Bodakh, George Konitsiotis, Antonio D. Thinon, Emmanuelle Rodgers, Ursula R. Owens, Raymond J. Magee, Anthony I. Tate, Edward W. Data Brief Data Article In this data article we describe synthetic and characterisation data for four members of the 5-acyl-6,7-dihydrothieno[3,2-c]pyridine (termed “RU-SKI”) class of inhibitors of Hedgehog acyltransferase, including associated NMR spectra for final compounds. RU-SKI compounds were selected for synthesis based on their published high potencies against the enzyme target. RU-SKI 41 (9a), RU-SKI 43 (9b), RU-SKI 101 (9c), and RU-SKI 201 (9d) were profiled for activity in the related article “Click chemistry armed enzyme linked immunosorbent assay to measure palmitoylation by Hedgehog acyltransferase” (Lanyon-Hogg et al., 2015) [1]. (1)H NMR spectral data indicate different amide conformational ratios between the RU-SKI inhibitors, as has been observed in other 5-acyl-6,7-dihydrothieno[3,2-c]pyridines. The synthetic and characterisation data supplied in the current article provide validated access to the class of RU-SKI inhibitors. Elsevier 2016-02-10 /pmc/articles/PMC4816282/ /pubmed/27077078 http://dx.doi.org/10.1016/j.dib.2016.02.012 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Data Article Lanyon-Hogg, Thomas Masumoto, Naoko Bodakh, George Konitsiotis, Antonio D. Thinon, Emmanuelle Rodgers, Ursula R. Owens, Raymond J. Magee, Anthony I. Tate, Edward W. Synthesis and characterisation of 5-acyl-6,7-dihydrothieno[3,2-c]pyridine inhibitors of Hedgehog acyltransferase |
title | Synthesis and characterisation of
5-acyl-6,7-dihydrothieno[3,2-c]pyridine inhibitors of
Hedgehog acyltransferase |
title_full | Synthesis and characterisation of
5-acyl-6,7-dihydrothieno[3,2-c]pyridine inhibitors of
Hedgehog acyltransferase |
title_fullStr | Synthesis and characterisation of
5-acyl-6,7-dihydrothieno[3,2-c]pyridine inhibitors of
Hedgehog acyltransferase |
title_full_unstemmed | Synthesis and characterisation of
5-acyl-6,7-dihydrothieno[3,2-c]pyridine inhibitors of
Hedgehog acyltransferase |
title_short | Synthesis and characterisation of
5-acyl-6,7-dihydrothieno[3,2-c]pyridine inhibitors of
Hedgehog acyltransferase |
title_sort | synthesis and characterisation of
5-acyl-6,7-dihydrothieno[3,2-c]pyridine inhibitors of
hedgehog acyltransferase |
topic | Data Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4816282/ https://www.ncbi.nlm.nih.gov/pubmed/27077078 http://dx.doi.org/10.1016/j.dib.2016.02.012 |
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