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Oximes bisquaternary

Musilek, K., Komloova, M., Holas, O., et al., 2011b. Mono-oxime bisquaternary acetylcholinesterase reactivators with prop-l,3-diyl linkage-preparation, in vitro screening and molecular docking. Bioorg. Med. Chem. 19, 754-762. [Pg.1086]

Ashani Y, RadicZ, Tsigelny letal.( 995). Amino acid residues controlling reactivation of organophos-phonyl conjugates of acetylcholinesterase by mono- and bisquaternary oximes../ Biol Chem, 270, 6370-6380. [Pg.322]

Luo C, Ashani Y and Doctor BP (1998a). Acceleration of oxime-induced reactivation of organophosphate -inhibited fetal bovine serum acetylcholinesterase by monoquaternary and bisquaternary ligands. Mol Pharmacol, 53, 718-726. [Pg.326]

The current standard treatment with reactivators includes different types of oximes with a similar basic structure differing by the number of pyridi-nium rings and by the position of the oxime group in the pyridinium ring. From the common oximes, mono- and bisquaternary pyridinium oximes are frequently used, such as pralidoxime, obidoxime, trimedoxime, methoxime,... [Pg.191]

FIGURE 72.15 Monoquaternary and bisquaternary oximes prepared by Musilek et al. (2006b,c). [Pg.1077]

Lundy, P.M., Raveh, L., Amitai, G., 2006. Development of the bisquaternary oxime HI-6 toward clinical use in the treatment of organophosphate nerve agent poisoning. Toxicol. Rev. 25, 231-243. [Pg.1086]


See other pages where Oximes bisquaternary is mentioned: [Pg.640]    [Pg.640]    [Pg.643]    [Pg.644]    [Pg.1316]    [Pg.192]   
See also in sourсe #XX -- [ Pg.1083 ]




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