Search Results - "Kormilitsyn, B N"

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    Substrate Specificity of Cholinesterases in Various Representatives of the Animal Kingdom by Basova, N. E., Kormilitsyn, B. N., Perchenok, A. Yu, Rozengart, E. V., Saakov, V. S., Suvorov, A. A.

    “…This review summarizes the literature data as well as experimental results obtained at our Institute over a period of 50 years on the substrate specificity of…”
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    New Acylate and Thioacylate Effectors of Mammalian Cholinesterases Based on Cyclic Ammonium Alcohols Containing Elements of the Anabasine Structure by Basova, N. E., Kormilitsyn, B. N., Perchenok, A. Yu, Rozengart, E. V., Saakov, V. S., Suvorov, A. A.

    “…We report a pioneering analysis of the interaction between mammalian cholinesterases and 36 acylates and thioacylates of ammonium alcohols with different…”
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    Activities of Tetramethylene-Bis-Onium Reversible Cholinesterase Inhibitors as Influenced by the Nature of the Onium Atom by Basova, N. E., Kormilitsyn, B. N., Perchenok, A. Yu, Rozengart, E. V., Saakov, V. S., Suvorov, A. A.

    Published in Pharmaceutical chemistry journal (01-11-2016)
    “…Inorganic tetramethylene bis -onium compounds were studied as reversible inhibitors of various cholinesterases (ChE), i.e., human erythrocyte acetyl-ChE, horse…”
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    Tetramethonium derivatives as reversible inhibitors of various cholinesterases by Basova, N. E., Kormilitsyn, B. N., Perchenok, A. Yu, Rozengart, E. V., Saakov, V. S., Suvorov, A. A.

    “…To study the effect of the onium atom nature on anticholinesterase efficiency, we tested elementorganic derivatives of tetramethylenbisonium compounds as…”
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    Inhibitory effect of benzimidazole derivatives on cholinesterases of animals in the presence of different substrates by Basova, N E, Kormilitsyn, B N, Perchenok, A Iu, Rosengart, E V, Saakov, V S, Suvorov, A A

    Published in Ukrainian biochemical journal (01-09-2014)
    “…Specifically synthesized group of benzimidazole derivatives possessing varying degrees of delocalization of the positive charge in the cation group of the…”
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    Transferase activity of horse blood serum cholinesterase at hydrolysis of 1-methyl-8-acetoxychinolium iodide in the presence of aliphatic alcohols by Basova, N E, Kormilitsyn, B N, Perchenok, A Yu, Rozengart, E V, Saakov, V S, Suvorov, A A

    “…To check whether the horse blood serum butyrylcholinesterase expresses transferase activity at the complex ester hydrolysis in the presense of several…”
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    Transferase activity of horse blood serum cholinesterase at hydrolysis of 1-methyl-8-acetoxychinolinium iodide in the presence of aliphatic alcohols by Basova, N. E., Kormilitsyn, B. N., Perchenok, A. Yu, Rozengart, E. V., Saakov, V. S., Suvorov, A. A.

    “…The study was performed to check whether the horse blood serum butyrylcholinesterase expresses transferase activity in the presence of several low-molecular…”
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    Amine Oxidases of Microorganisms by Yagodina, O V, Nikol'skaya, E B, Khovanskikh, A E, Kormilitsyn, B N

    “…The review of works on amine oxidases of microorganisms is presented. Preparation, physical-chemical and kinetic properties of amine oxidases from…”
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    How aliphatic alcohols and pH affect reactivity of horse blood serum cholinesterase at its interaction with organophosphorus inhibitors by Basova, N. E., Kormilitsyn, B. N., Perchenok, A. Yu, Rozengart, E. V., Saakov, V. S., Suvorov, A. A.

    “…There was studied action of aliphatic alcohols (ethanol, propanol, isopropanol, n -butanol, isobutanol, sec -butanol, tert -butanol), and pH on various kinds…”
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    Ligands of cholinesterases of ephedrine and pseudoephedrine structure by Basova, N. E., Kormilitsyn, B. N., Perchenok, A. Yu, Rozengart, E. V., Saakov, V. S., Suvorov, A. A.

    “…The paper is a review of literature data on interaction of erythrocytic acetylcholinesterase and of mammalian blood serum butyrylcholinesterase with a group of…”
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    Sensitivity of Cholinesterases of Different Origin to Organophosphorus Inhibitors with S-Alkyl Radical of Different Length by Kormilitsyn, B. N., Moralev, S. N., Khovanskikh, A. E., Dalimov, D. N.

    “…An antienzyme potency of 18 organophosphorus inhibitors (OPI), S-alkyl derivatives of thiophosphoric and thiophosphonic acids, to acetylcholinesterase (AChE)…”
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