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...

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Main Authors: Thomas Lanyon-Hogg, Naoko Masumoto, George Bodakh, Antonio D. Konitsiotis, Emmanuelle Thinon, Ursula R. Rodgers, Raymond J. Owens, Anthony I. Magee, Edward W. Tate
Format: Article
Language:English
Published: Elsevier 2016-06-01
Series:Data in Brief
Online Access:http://www.sciencedirect.com/science/article/pii/S2352340916300348
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author Thomas Lanyon-Hogg
Naoko Masumoto
George Bodakh
Antonio D. Konitsiotis
Emmanuelle Thinon
Ursula R. Rodgers
Raymond J. Owens
Anthony I. Magee
Edward W. Tate
author_facet Thomas Lanyon-Hogg
Naoko Masumoto
George Bodakh
Antonio D. Konitsiotis
Emmanuelle Thinon
Ursula R. Rodgers
Raymond J. Owens
Anthony I. Magee
Edward W. Tate
author_sort Thomas Lanyon-Hogg
collection DOAJ
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]. 1H 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. Keywords: Synthesis, Inhibitors, Hedgehog acyltransferase, Conformation
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spelling doaj.art-4bfe980dcf9a43e8805f3661c29e69812022-12-22T01:00:00ZengElsevierData in Brief2352-34092016-06-017257281Synthesis and characterisation of 5-acyl-6,7-dihydrothieno[3,2-c]pyridine inhibitors of Hedgehog acyltransferaseThomas Lanyon-Hogg0Naoko Masumoto1George Bodakh2Antonio D. Konitsiotis3Emmanuelle Thinon4Ursula R. Rodgers5Raymond J. Owens6Anthony I. Magee7Edward W. Tate8Department of Chemistry, Imperial College London, SW7 2AZ, UK; Institute of Chemical Biology, Imperial College London, SW72AZ, UKDepartment of Chemistry, Imperial College London, SW7 2AZ, UK; Institute of Chemical Biology, Imperial College London, SW72AZ, UKDepartment of Chemistry, Imperial College London, SW7 2AZ, UK; Institute of Chemical Biology, Imperial College London, SW72AZ, UKMolecular Medicine Section, National Heart & Lung Institute, Imperial College London, London SW7 2AZ, UKDepartment of Chemistry, Imperial College London, SW7 2AZ, UK; Institute of Chemical Biology, Imperial College London, SW72AZ, UKMolecular Medicine Section, National Heart & Lung Institute, Imperial College London, London SW7 2AZ, UKOxford Protein Production Facility UK, The Research Complex at Harwell, Rutherford Appleton Laboratory, Harwell Science & Innovation Centre, Harwell OX11 0FA, UKMolecular Medicine Section, National Heart & Lung Institute, Imperial College London, London SW7 2AZ, UK; Corresponding author at: Molecular Medicine Section, National Heart & Lung Institute, Imperial College London, London SW7 2AZ, UK. Tel.: +44 20 7594 3135.Department of Chemistry, Imperial College London, SW7 2AZ, UK; Institute of Chemical Biology, Imperial College London, SW72AZ, UK; Corresponding author at: Institute of Chemical Biology, Department of Chemistry, Imperial College London, London SW7 2AZ, UK. Tel.: +44 20 7594 3752.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]. 1H 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. Keywords: Synthesis, Inhibitors, Hedgehog acyltransferase, Conformationhttp://www.sciencedirect.com/science/article/pii/S2352340916300348
spellingShingle Thomas Lanyon-Hogg
Naoko Masumoto
George Bodakh
Antonio D. Konitsiotis
Emmanuelle Thinon
Ursula R. Rodgers
Raymond J. Owens
Anthony I. Magee
Edward W. Tate
Synthesis and characterisation of 5-acyl-6,7-dihydrothieno[3,2-c]pyridine inhibitors of Hedgehog acyltransferase
Data in Brief
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
url http://www.sciencedirect.com/science/article/pii/S2352340916300348
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