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Esterase acetylcholine

Application of the CCM to small sets (n < 6) of enzyme inhibitors revealed correlations between the inhibitory activity and the chirality measure of the inhibitors, calculated by Eq. (26) for the entire structure or for the substructure that interacts with the enzyme (pharmacophore) [41], This was done for arylammonium inhibitors of trypsin, Di-dopamine receptor inhibitors, and organophosphate inhibitors of trypsin, acetylcholine esterase, and butyrylcholine esterase. Because the CCM values are equal for opposite enantiomers, the method had to be applied separately to the two families of enantiomers (R- and S-enantiomers). [Pg.419]

Katz E, WiUner 1, Wang J (2004) Electroanalytical and bioelectroanalytical systems based on metal and semiconductor nanoparticles. Electroanalysis 16 19-44 Pardo-Yissar V, Katz E, Wasserman J, Willner 1 (2003) Acetylcholine esterase-labeled CdS nanoparticles on electrodes Photoelectrochemical sensing of the enzyme inhibitors. J Am Chem Soc 125 622-623... [Pg.348]

Diol bonded silica Glucosamine, bovine serum albumin, immunoglobulin, acetylcholine esterase, horse liver alcohol dehydrogenase [136]... [Pg.173]

Pontine cholinergic agonists and acetylcholine esterase inhibitors... [Pg.112]

Trettnak W., Reininger F., Zinterl E., Wolfbeis O.S., Fiber Optic Remote Detection of Pesticides and Related Inhibitors of the Enzyme Acetylcholine Esterase, Sensor Actuat B-Chem 1993 11 87. [Pg.44]

A particular interest for clinical applications was a possibility for detection of dopamine by its oxidation on nickel [19], cobalt [65], and osmium [66] hexacyanofer-ates. Except for oxidation of dopamine, cobalt and osmium hexacyanoferrates were active in oxidation of epinephrine and norepinephrine. For clinical analysis it is also important to carry out the detection of morphine on cobalt [67] and ferric [68] hexacyanoferrates, as well as the detection of oxidizable amino acids (cystein, methionine) by manganous [69] and ruthenium [70] hexacyanoferrate-modified electrodes. In general, oxidation of thiols was first shown for Prussian blue [71] and nickel hexacyanoferrate [72], This approach has been used for the detection of thiols in rat striatum microdialysate [73], Alternatively, the detection of thiocholine with Prussian blue was employed for pesticide determination in acetylcholine-esterase test [74],... [Pg.440]

Tor [7] developed a new method for the preparation of thin, uniform, self-mounted enzyme membrane, directly coating the surface of glass pH electrodes. The enzyme was dissolved in a solution containing synthetic prepolymers. The electrode was dipped in the solution, dried, and drained carefully. The backbone polymer was then cross-linked under controlled conditions to generate a thin enzyme membrane. The method was demonstrated and characterized by the determination of acetylcholine by an acetylcholine esterase electrode, urea by a urease electrode, and penicillin G by a penicillinase electrode. Linear response in a wide range of substrate concentrations and high storage and operational stability were recorded for all the enzymes tested. [Pg.557]

The same group reported in 1986 a sensitive and selective HPLC method employing CL detection utilizing immobilized enzymes for simultaneous determination of acetylcholine and choline [187], Both compounds were separated on a reversed-phase column, passed through an immobilized enzyme column (acetylcholine esterase and choline oxidase), and converted to hydrogen peroxide, which was subsequently detected by the PO-CL reaction. In this period, other advances in this area were carried out such as the combination of solid-state PO CL detection and postcolumn chemical reaction systems in LC [188] or the development of a new low-dispersion system for narrow-bore LC [189],... [Pg.30]

Choline, acetylcholine Choline oxidase Acetylcholine esterase 48-50... [Pg.158]

A variety of enzymes (such as acetylcholine esterase, Porcine pancreatic lipase, Pseudomonas cepacia lipase, and Candida antarcita lipase) have been found useful in the preparation of enantiomerically pure cyclopentenol (+)-2 from 1. The enantiomeric (—)-2 has been prepared from diol 4 by enzymatic acetylation catalyzed by VP-345 with isopropenyl acetate in an organic medium. The key intermediate cyclopentanones (+)-6, (—)-6, 7, and 8, which are useful in the preparation of many bioactive molecules, can be obtained from 3 and 5 via routine chemical transformations.7... [Pg.453]

Brzezinski J, Ludwicki K. 1973. The interrelationship of the changes of acetylcholine esterase and catecholamines blood and urine levels in rats poisoned with Disyston. Pol J Pharmacol Pharm 25 313-316. [Pg.179]

The work that paved the way toward enzymatic inhibition was published in the early 1990s by Wudl and coworkers (Schinazietal., 1993 Friedmanetal., 1993 Sijbesma et al., 1993) and since then studies regarding antiviral activity, mainly HIV-protease inhibition, have been carried out to find active compounds. Up to now, the most effective fullerene derivatives are the trans-2, -dimethy 1-bis-fulleropyrrolidin-ium salt (Fig. 1.4) (Marchesan et al., 2005) and the dendrofullerene reported by Hirsch (Schuster et al., 2000) both of them present an ECJ0 of 0.2pM. Also HIV reverse transcriptase can be inhibited by, -dimcthyl-bis-fulleropyrrolidinium salts (Mashino et al., 2005). The same compounds are also active against acetylcholine esterase (AChE), an enzyme that hydrolyzes a very important neurotransmitter. [Pg.10]

Aeetylacetone, 32 248-249 hydrogenation, 32 259-262 Acetylcholine esterase, 20 344, 367 Acetylene adsorption complexes, 31 6-7 potential dependence, 30 258 catalytic oxidation of, for oxygen manufacture, 3 107... [Pg.37]

The most outstanding example illustrating this strategy came from the team of Alain Friboulet and Daniel Thomas, who produced anti-idiotype antibodies against a monoclonal antibody AE2 that was a competitive inhibitor of acetylcholine esterase. One of the selected antibodies, 9A8, catalyzes the hydrolysis of acetylthio-choline with a pseudo first-order rate constant /feat = 81 and a factor of acceleration of 4.2 x 10 . These remarkable parameters, which are only two orders of magnitude lower when compared to those of the enzyme, make abzyme 9A8 the most powerful abzyme known until now. [Pg.346]

The mode of action of the isobutylamides is unknown, although Miyakado et al. found that several isobutylamides (i.e. pipercide and related compounds) caused repetitive discharge when the nerve cord of the cockroach, Periplaneta americana was stimulated. We found that fagaramide was inactive as an acetylcholine esterase inhibitor in an m vitro assay(unpublished dat a). [Pg.170]

Lin BQ, Ji H, Li P, Fang W, Jiang Y, Inhibitors of acetylcholine esterase in vitro screening of steroidal alkaloids from Fritillaria species, Planta Afc 72 814—818,... [Pg.423]

Selected entries from Methods in Enzymology [vol, page(s)] Sulfonylation reaction, 11, 706 reaction kinetics, 11, 707 second-order rate constants for inactivation of chymotrypsin, trypsin, and acetylcholine esterase by PMSE and related sulfonylat-ing agents, 11, 707 reactivation of PMS-chymotrypsin, 11, 710 as inhibitor [of calcium-activated factor, 80, 674 of cathepsin G, 80, 565 of crayfish trypsin, 80, 639 of elastase, 80, 587 of pro-lylcarboxypeptidase, 80, 465 of protease Re, 80, 691 of protease So, 80, 695 of protein C, 80, 329] proteolysis, 76, 7. [Pg.548]

Assays of acetyl- and butyrylcholine esterases inhibition, as well as of modulation of calcium channels and nicotinic receptors have been conducted in vivo. Moreover, their interaction with the active center of acetylcholine esterase has been simulated by molecular dynamics. For synthesized compounds the IC50 of acetylcholine esterase inhibition was about 9 X M, and for the most active the value was four to five times... [Pg.244]

In connection with research on oximes as reactivators of phosphorylated acetylcholine esterase, a number of studies have shown that introduction of cationic micelles such... [Pg.832]

Ions and channels Acetylcholine esterase Receptors Microbial activity Schizonticlde activity St ffVlatlon and Inhibiting... [Pg.184]

The alkaloids which influence acetylcholine esterase activity are eserine, galan-thamine, nicotine, lobeline and tubocurarine. All of these alkaloids are very active. [Pg.185]

Eserine blocks acetylcholine esterase. This alkaloid may be used to decrease possible negative side effects connected to the use of other drugs, for example that of atropine. [Pg.185]

Galanthamine also blocks acetylcholine esterase activity. One of the new applications of galanthamine is in a treatment of Alzheimer s disease. Moreover, this alkaloid can be used in decreasing negative side effects caused by applications of non-depolarizing alkaloids, for example those of tubocurarine. [Pg.185]

The inhibitors of the acetylcholine esterase reduce the rate of hydrolysis of acetylcholine since they... [Pg.294]

The ester of the phosphorous acid or organophos-phorsus inhibitors of the acetylcholine esterase phos-phorylate serine in the active center of the enzyme. The phosphorylated enzyme is extremely stable, resulting in an irreversible inhibition. The duration of action of this compounds is determined by the rate of enzyme synthesis de novo. [Pg.294]


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Acetylcholine esterase assay

Acetylcholine esterase functions

Acetylcholine esterase inhibition

Acetylcholine esterase inhibitors

Acetylcholine esterase inhibitors (AChE

Acetylcholine esterase mechanisms

Acetylcholine esterase, active serine, mechanism

Acetylcholine esterase, experiment with

Choline acetylcholine esterase electrode

Enzymes acetylcholine esterase

Esterase

Esterases

Esterases acetylcholin esterase

Esterases esterase

Regulation of acetylcholine esterase

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