Inhibition of acetylcholinesterase by 14 achiral and five chiral imidazole derivates
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
20335028
DOI
10.1016/j.biortech.2010.03.017
PII: S0960-8524(10)00471-2
Knihovny.cz E-zdroje
- MeSH
- acetylcholinesterasa chemie MeSH
- aktivace enzymů MeSH
- cholinesterasové inhibitory chemie MeSH
- Electrophorus metabolismus MeSH
- imidazoly chemie MeSH
- stabilita enzymů MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- acetylcholinesterasa MeSH
- cholinesterasové inhibitory MeSH
- imidazole MeSH Prohlížeč
- imidazoly MeSH
Homological series of 14 achiral derivates and series of five chiral derivates of imidazole were tested in vitro as inhibitors of hydrolysis of acetylcholine using enzyme preparation of acetylcholinesterase from electric eel. The batch stirred reactor at 25 degrees C, pH 8 (phosphate buffer), ionic strength 0.11 M and catalytic activity of the enzyme preparation 0.14 U ml(-1) of the reaction mixture were used. The temporal dependences of actual concentrations of acetylcholine, choline and acetic acid were determined by an original HPLC method. For all used inhibitors, these time dependences conform with the probability of more than 90% to the model of competitive irreversible inhibition. All kinetic constants including k(3) defining the rate of inhibition (0.38-5.3M(-1)s(-1)) and qualified estimation of the absolute acetylcholinesterase concentration in the reaction mixture (40-110 nM) were determined.
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