3-Hydroxyquinuclidinium derivatives: synthesis of compounds and inhibition of acetylcholinesterase (CROSBI ID 81258)
Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija
Podaci o odgovornosti
Reiner, Elsa ; Škrinjarić-Špoljar, Mira ; Dunaj, Sanja ; Simeon-Rudolf, Vera ; Primožič, Ines ; Tomić, Srđanka
engleski
3-Hydroxyquinuclidinium derivatives: synthesis of compounds and inhibition of acetylcholinesterase
Four compounds were prepared: 3-hydroxy-1-methylquinuclidinium iodide (I), 3-(N,N-dimethylcarbamoyloxy)-1-methylquinuclidinum iodide (II), and two conjugates of I and II with 2-hydroxyiminomethyl-3-methylimidazole in which two parts of the molecule were linked by -CH"2"-O-CH"2" - (III and IV). III and IV are new compounds and their synthesis and physical data were given. All compounds were tested as inhibitors of human erythrocyte acetylcholinesterase (EC 3.1.1.7, AChE). The enzyme activity was measured in 0.1 M phosphate buffer (pH 7.4) at 10 oC and 37 oC with acetylthiocholine (ATCh) as the substrate. The obtained enzyme/inhibitor dissociation constants were between 0.05 and 0.5 mM at 10 oC and between 0.2 and 0.6 mM at 37 oC. At both temperatures compounds III and IV had higher affinities for the enzyme than compounds I and II and this difference was more pronounced at l0 oC than at 37 oC. The carbamates II and IV were also progressive AChE inhibitors. For compound II the rate constants of inhibition were 6300 and 2020 M^1 min^1 at 37 oC and l0 oC respectively. Compound IV was a very weak carbamoylating agent with rate constants of inhibition 100 and 63M^1 min^1 at 37 oC and l0 oC respectively. The oxime group in compounds III and IV hydrolysed ATCh at a rate of 23 and 3.2 M^1 min-1 at 37 oC and l0 oC respectively.
quinuclidinium-imidazolium compounds-quinuclidinium carbamates-sinthesis; reversible and progressive acetylcholinesterase inhibition
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano
nije evidentirano