Search Results - "Sherstobitov, O E"

Alkylating derivative of hexadecamethonium protects muscle synaptic acetylcholinesterase against inhibition by Danilov, Anatoly F., Grigoriev, Victor M., Prokhorenko, Natalya K., Sherstobitov, Oleg E.

“…The action of the alkylating derivative of hexadecamethonium on frog neuromuscular transmission was studied with the help of intracellular microelectrodes…”
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Synthesis and anticholinesterase activity of S-ethynyl dialkylthiophosphates with cyclic substituents at the acetylenic bond by Godovikov, N. N., Vikhreva, L. A., Darisheva, A. M., Balashova, I. K., Moralev, S. N., Brestkin, A. P., Rozengart, V. I., Sherstobitov, O. E., Kabachnik, M. I.

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Synthesis and anticholinesterase activity of S-alkynyl diethyl thiophosphates containing hydrophobic or onium groups in the alkylthiol radical by Godovikov, N. N., Vikhreva, L. A., Balashova, E. K., Brestkin, A. P., Moralev, S. N., Rozengart, V. I., Sherstobitov, O. E., Kabachnik, M. I.

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Synthesis and anticholine esterase properties of S-ethynyl esters of thiophosphoric acids by Godovikov, N. N., Vikhreva, L. A., Babasheva, K. K., Sherstobitov, O. E., Balashova, E. K., Kugusheva, L. I., Rozengart, V. I., Brestkin, A. P., Kabachnik, M. I.

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Alkylating derivative of hexadecamethonium protects muscle synaptic acetylcholinesterase against inhibition by DANILOV, A. F, GRIGORIEV, V. M, PROKHORENKO, N. K, SHERSTOBITOV, O. E

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The effect of pH and reversible inhibitors on decarbamylation of acetylcholinesterase by Kugusheva, L I, Rozengart, V I, Sherstobitov, O E

“…Decarbamylation rate of membrane-bound methyl- and dimethyl-carbamylated acetylcholinesterase of human erythrocytes and bovine brain is reliably 1.1-1.6 times…”
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Interaction of membrane-bound and solubilized erythrocyte acetylcholinesterase with carbamates by Kugusheva, L I, Rozengart, V I, Sherstobitov, O E

“…Physostigmine and neostigmine methylsulphate are shown to be the most strong inhibitors of acetylcholine esterase of human erythrocytes. The action of baigon…”
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Effect of environment on allosteric properties of acetylcholinesterase by Freĭdlin, T S, Balashova, E K, Rozengart, V I, Sherstobitov, O E

“…In the presence of organophosphorus inhibitors (OPI) AChE inhibition is initiated at a lower concentration of ACh; the plot reaction rate versus substrate…”
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High selectivity in the effect of organophosphorus insecto-acaricides containing the acetylene bond on Arthropoda by Vikhreva, L A, Godovikov, N N, Rozengart, V I, Sherstobitov, O E, Kabachnik, M I

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Substances with cholinopotentiating properties by Ioffe, D. V., Kuznetsov, S. G., Solov'eva, T. V., Shvarts, T. L., Sherstobitov, O. E.

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Intracellular distribution of phosphoorganic cholinesterase inhibitors in rat brain by Pevzner, L, Balashova, E K, Kruglova, E E, Rozengart, V I, Sherstobitov, O E

“…Content of organophosphorous inhibitors (with the structure RO/CH3/P/O/SC2H4SC2H5) of cholinesterase as well as their hydrophobic properties (distribution…”
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Binding of phosphoorganic cholinesterase inhibitors in rat brain tissue by Balashova, E K, Pevzner, D L, Rozengart, V I, Sherstobitov, O E, Abduvarkhabov, A A

“…Hydrophobity (coefficient in distribution in the hexane water system) and the content of cholinesterase organophosphorous inhibitors (OPI) of the structure Ro…”
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The distribution of cholinesterase charged phosphorganic inhibitors and their uncharged analogues in tissues by Balashova, B A, Pevzner, D L, Rozengart, V I, Sherstobitov, O E

“…The article deals with the hydrophobic character (distribution coefficient in the systems hexane - water and chloroform - water) and certain peculiarities of…”
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Effect of charge-free organophosphorus inhibitors on intensifying the substrate inhibition of acetylcholinesterase by Balashova, E K, Rozengart, V I, Freĭdlin, T S, Sherstobitov, O E

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Forms of deposition of phosphoorganic cholinesterase inhibitors in the brain by Balashova, E K, Pevzner, D L, Rozengart, V I, Sherstobitov, O E, Abduvakhobov, A A

“…The content and hydrophobic properties (distribution coefficient in hexan : water) of organophosphorus inhibitors OPT of the following structure--R-O…”
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Hydrophobic nature of organophosphorus cholinesterase inhibitors and some characteristics of their distribution in the body by Balashova, E K, Pevzner, D L, Rozengart, V I, Sherstobitov, O E

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Some differences in the effects of anticholinesterase compounds on nicotine and arecoline sensitivity in mice and rabbits by Erkova, A I, Savateev, N V, Sofronov, G A, Sherstobitov, O E

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Synthesis and anticholinesterase activity of acetylene organophosphorus compounds by Balashova, E K, Brestkin, A P, Zhukovskiĭ, Iu G, Rozengart, V I, Sherstobitov, O E

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Determination of hydrophobic organic phosphorus cholinesterase inhibitors in the blood by Balashova, E K, Pevzner, D L, Rozengart, V I, Sherstobitov, O E

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