Grid-Type Quaternary Metallosupramolecular Compounds Inhibit Human Cholinesterases through Dynamic Multivalent Interactions
Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review
Author(s)
Detail(s)
Original language | English |
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Article number | e202200456 |
Journal / Publication | ChemBioChem |
Volume | 23 |
Issue number | 23 |
Online published | 4 Oct 2022 |
Publication status | Published - 5 Dec 2022 |
Externally published | Yes |
Link(s)
Abstract
We report the implementation of coordination complexes containing two types of cationic moieties, i. e. pyridinium and ammonium quaternary salt, as potential inhibitors of human cholinesterase enzymes. Utilization of ligands containing NNO-coordination site and binding zinc metal ion allowed mono- and tetra-nuclear complexes to be obtained with corner and grid structural type, respectively, thus affecting the overall charge of the compounds (from +1 to +8). We were able to examine for the first time the multivalency effect of metallosupramolecular species on their inhibitory abilities towards acetylcholinesterase (AChE) and butyrylcholinesterase (BChE). Importantly, resolution of the crystal structures of the obtained enzyme-substrate complexes provided a better understanding of the inhibition process at the molecular level. © 2022 Wiley-VCH GmbH.
Research Area(s)
- acetylcholinesterases, butyrylcholinesterases, inhibitors, supramolecular chemistry, X-ray structures
Citation Format(s)
Grid-Type Quaternary Metallosupramolecular Compounds Inhibit Human Cholinesterases through Dynamic Multivalent Interactions. / Nachon, Florian; Brazzolotto, Xavier; Dias, José et al.
In: ChemBioChem, Vol. 23, No. 23, e202200456, 05.12.2022.
In: ChemBioChem, Vol. 23, No. 23, e202200456, 05.12.2022.
Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review