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Expanding the library of divalent fucosidase inhibitors with polyamino and triazole-benzyl bridged bispyrrolidines.
- Source :
-
Organic & biomolecular chemistry [Org Biomol Chem] 2016 Mar 28; Vol. 14 (12), pp. 3212-20. - Publication Year :
- 2016
-
Abstract
- A small library of divalent fucosidase inhibitors containing pyrrolidine motifs and separated by polyamino and triazole-benzylated spacers was prepared and evaluated as α-fucosidase inhibitors. Although a weak multivalent effect was observed in polyamino derived dimers, useful structural information can be deduced about the length of the bridge, the number of nitrogen atoms present and the moieties close to the pyrrolidine. Within these investigations one of the best α-fucosidase inhibitors containing a pyrrolidine framework was obtained (18, Ki = 3.7 nM).
- Subjects :
- Dose-Response Relationship, Drug
Enzyme Inhibitors chemical synthesis
Humans
Molecular Conformation
Pyrrolidines chemical synthesis
Structure-Activity Relationship
alpha-L-Fucosidase metabolism
Enzyme Inhibitors chemistry
Enzyme Inhibitors pharmacology
Pyrrolidines chemistry
Pyrrolidines pharmacology
alpha-L-Fucosidase antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 1477-0539
- Volume :
- 14
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Organic & biomolecular chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 26906450
- Full Text :
- https://doi.org/10.1039/c6ob00212a