Structural essentials for β-N-acetylhexosaminidase inhibition by amides of prolines, pipecolic and azetidine carboxylic acids.

Autor:	Glawar AF; Chemistry Research Laboratory, 12 Mansfield Road, Oxford, OX1 3TA, UK. sarah.jenkinson@chem.ox.ac.uk and Oxford Glycobiology Institute, University of Oxford, South Parks Road, Oxford, OX1 3QU, UK., Martínez RF; Chemistry Research Laboratory, 12 Mansfield Road, Oxford, OX1 3TA, UK. sarah.jenkinson@chem.ox.ac.uk., Ayers BJ; Chemistry Research Laboratory, 12 Mansfield Road, Oxford, OX1 3TA, UK. sarah.jenkinson@chem.ox.ac.uk., Hollas MA; Chemistry Research Laboratory, 12 Mansfield Road, Oxford, OX1 3TA, UK. sarah.jenkinson@chem.ox.ac.uk., Ngo N; Chemistry Research Laboratory, 12 Mansfield Road, Oxford, OX1 3TA, UK. sarah.jenkinson@chem.ox.ac.uk., Nakagawa S; Department of Hospital Pharmacy, University of Toyama, 2630 Sugitani, Toyama 930-0194, Japan. kato@med.u-toyama.ac.jp., Kato A; Department of Hospital Pharmacy, University of Toyama, 2630 Sugitani, Toyama 930-0194, Japan. kato@med.u-toyama.ac.jp., Butters TD; Oxford Glycobiology Institute, University of Oxford, South Parks Road, Oxford, OX1 3QU, UK., Fleet GW; Chemistry Research Laboratory, 12 Mansfield Road, Oxford, OX1 3TA, UK. sarah.jenkinson@chem.ox.ac.uk and Oxford Glycobiology Institute, University of Oxford, South Parks Road, Oxford, OX1 3QU, UK., Jenkinson SF; Chemistry Research Laboratory, 12 Mansfield Road, Oxford, OX1 3TA, UK. sarah.jenkinson@chem.ox.ac.uk.
Jazyk:	angličtina
Zdroj:	Organic & biomolecular chemistry [Org Biomol Chem] 2016 Nov 08; Vol. 14 (44), pp. 10371-10385.
DOI:	10.1039/c6ob01549b
Abstrakt:	This paper explores the computer modelling aided design and synthesis of β-N-acetylhexosaminidase inhibitors along with their applicability to human disease treatment through biological evaluation in both an enzymatic and cellular setting. We investigated the importance of individual stereocenters, variations in structure-activity relationships along with factors influencing cell penetration. To achieve these goals we modified nitrogen heterocycles in terms of ring size, side chains present and ring nitrogen derivatization. By reducing the inhibitor interactions with the active site down to the essentials we were able to determine that besides the established 2S,3R trans-relationship, the presence and stereochemistry of the CH 2 OH side chain is of crucial importance for activity. In terms of cellular penetration, N-butyl side chains favour cellar uptake, while hydroxy- and carboxy-group bearing sidechains on the ring nitrogen retarded cellular penetration. Furthermore we show an early proof of principle study that β-N-acetylhexosaminidase inhibitors can be applicable to use in a potential anti-invasive anti-cancer strategy.
Databáze:	MEDLINE
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