1,4-Dideoxy-1,4-imino-D- and L-lyxitol-based inhibitors bind to Golgi α-mannosidase II in different protonation forms.


Journal

Organic & biomolecular chemistry
ISSN: 1477-0539
Titre abrégé: Org Biomol Chem
Pays: England
ID NLM: 101154995

Informations de publication

Date de publication:
23 11 2022
Historique:
pubmed: 3 11 2022
medline: 25 11 2022
entrez: 2 11 2022
Statut: epublish

Résumé

The development of effective inhibitors of Golgi α-mannosidase II (GMII, E.C.3.2.1.114) with minimal off-target effects on phylogenetically-related lysosomal α-mannosidase (LMan, E.C.3.2.1.24) is a complex task due to the complicated structural and chemical properties of their active sites. The p

Identifiants

pubmed: 36322142
doi: 10.1039/d2ob01545e
pmc: PMC7614232
mid: EMS170523
doi:

Substances chimiques

mannosyl-oligosaccharide 1,3 - 1,6-alpha-mannosidase EC 3.2.1.114
alpha-Mannosidase EC 3.2.1.24
arabitol YFV05Y57M9
Mannosidases EC 3.2.1.-
Enzyme Inhibitors 0
Amino Acids 0
Amantadine BF4C9Z1J53

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

8932-8943

Subventions

Organisme : Austrian Science Fund FWF
ID : P 29466
Pays : Austria

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Auteurs

Juraj Kóňa (J)

Institute of Chemistry, Center for Glycomics, Slovak Academy of Sciences, Dúbravska cesta 9, 845 38 Bratislava, Slovakia. chemkona@savba.sk.
Medical Vision, Civic Research Association, Záhradnícka 4837/55, 82108 Bratislava, Slovakia.

Sergej Šesták (S)

Institute of Chemistry, Center for Glycomics, Slovak Academy of Sciences, Dúbravska cesta 9, 845 38 Bratislava, Slovakia. chemkona@savba.sk.

Iain B H Wilson (IBH)

Department of Chemistry, University of Natural Resources and Life Sciences, 1190 Vienna, Austria.

Monika Poláková (M)

Institute of Chemistry, Center for Glycomics, Slovak Academy of Sciences, Dúbravska cesta 9, 845 38 Bratislava, Slovakia. chemkona@savba.sk.

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Classifications MeSH