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Synthesis and biological evaluation of nojirimycin- and pyrrolidine-based trehalase inhibitors

A small set of nojirimycin- and pyrrolidine-based iminosugar derivatives has been synthesized and evaluated as potential inhibitors of porcine and insect trehalases. Compounds 12, 13 and 20 proved to be active against both insect and porcine trehalases with selectivity towards the insect glycosidase...

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Autores principales: Bini, Davide, Cardona, Francesca, Forcella, Matilde, Parmeggiani, Camilla, Parenti, Paolo, Nicotra, Francesco, Cipolla, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3326631/
https://www.ncbi.nlm.nih.gov/pubmed/22509223
http://dx.doi.org/10.3762/bjoc.8.58
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author Bini, Davide
Cardona, Francesca
Forcella, Matilde
Parmeggiani, Camilla
Parenti, Paolo
Nicotra, Francesco
Cipolla, Laura
author_facet Bini, Davide
Cardona, Francesca
Forcella, Matilde
Parmeggiani, Camilla
Parenti, Paolo
Nicotra, Francesco
Cipolla, Laura
author_sort Bini, Davide
collection PubMed
description A small set of nojirimycin- and pyrrolidine-based iminosugar derivatives has been synthesized and evaluated as potential inhibitors of porcine and insect trehalases. Compounds 12, 13 and 20 proved to be active against both insect and porcine trehalases with selectivity towards the insect glycosidase, while compounds 10, 14 and 16 behaved as inhibitors only of insect trehalase. Despite the fact that the activity was found in the micromolar range, these findings may help in elucidating the structural features of this class of enzymes of different origin, which are still scarcely characterised.
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spelling pubmed-33266312012-04-16 Synthesis and biological evaluation of nojirimycin- and pyrrolidine-based trehalase inhibitors Bini, Davide Cardona, Francesca Forcella, Matilde Parmeggiani, Camilla Parenti, Paolo Nicotra, Francesco Cipolla, Laura Beilstein J Org Chem Full Research Paper A small set of nojirimycin- and pyrrolidine-based iminosugar derivatives has been synthesized and evaluated as potential inhibitors of porcine and insect trehalases. Compounds 12, 13 and 20 proved to be active against both insect and porcine trehalases with selectivity towards the insect glycosidase, while compounds 10, 14 and 16 behaved as inhibitors only of insect trehalase. Despite the fact that the activity was found in the micromolar range, these findings may help in elucidating the structural features of this class of enzymes of different origin, which are still scarcely characterised. Beilstein-Institut 2012-04-05 /pmc/articles/PMC3326631/ /pubmed/22509223 http://dx.doi.org/10.3762/bjoc.8.58 Text en Copyright © 2012, Bini 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 Full Research Paper
Bini, Davide
Cardona, Francesca
Forcella, Matilde
Parmeggiani, Camilla
Parenti, Paolo
Nicotra, Francesco
Cipolla, Laura
Synthesis and biological evaluation of nojirimycin- and pyrrolidine-based trehalase inhibitors
title Synthesis and biological evaluation of nojirimycin- and pyrrolidine-based trehalase inhibitors
title_full Synthesis and biological evaluation of nojirimycin- and pyrrolidine-based trehalase inhibitors
title_fullStr Synthesis and biological evaluation of nojirimycin- and pyrrolidine-based trehalase inhibitors
title_full_unstemmed Synthesis and biological evaluation of nojirimycin- and pyrrolidine-based trehalase inhibitors
title_short Synthesis and biological evaluation of nojirimycin- and pyrrolidine-based trehalase inhibitors
title_sort synthesis and biological evaluation of nojirimycin- and pyrrolidine-based trehalase inhibitors
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3326631/
https://www.ncbi.nlm.nih.gov/pubmed/22509223
http://dx.doi.org/10.3762/bjoc.8.58
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