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Journal Abstract Search

150 related items for PubMed ID: 9479388

  • 1. [Enzymatic identification of cholinesterase inhibitors].
    Nikol'skaia EB, Moralev SN.
    Zh Evol Biokhim Fiziol; 1997; 33(3):274-9. PubMed ID: 9479388
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  • 6. Substrate activation of butyrylcholinesterase and substrate inhibition of acetylcholinesterase by 3,3-dimethylbutyl-N-n-butylcarbamate and 2-trimethylsilyl-ethyl-N-n-butylcarbamate.
    Chiou SY, Wu YG, Lin YF, Lin LY, Lin G.
    J Biochem Mol Toxicol; 2007; 21(1):24-31. PubMed ID: 17366539
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  • 7. [Specificity of interaction with acetylcholinesterase and butyrylcholinesterase of choline analogs based on ephedrine and pseudoephedrine].
    Dalimov DN, Vaĭzburg GM, Abdullaeva LK, Abduvakhabov AA, Sadykov AS.
    Dokl Akad Nauk SSSR; 1986; 289(1):227-30. PubMed ID: 3732039
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  • 8. [Phosphorus atom availability and mechanism enzyme inhibiting effect of organophosphorous inhibitors of cholinesterases of various origin. Results of conformational and correlational analysis].
    Rozengart EV, Shestakova NN, Prokator SO, Basova NE.
    Zh Evol Biokhim Fiziol; 1999; 35(1):36-9. PubMed ID: 10399821
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  • 9. [Correlation of anticholinesterase activity of reversible peralkylated onium inhibitors of various acetylcholinesterases and geometric parameters of their molecules].
    Rozengart EB, Shestakova NN, Prokator SO, Basova NE.
    Zh Evol Biokhim Fiziol; 1998; 34(6):648-53. PubMed ID: 10188231
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  • 11. Design and synthesis of N-benzylpiperidine-purine derivatives as new dual inhibitors of acetyl- and butyrylcholinesterase.
    Rodríguez-Franco MI, Fernández-Bachiller MI, Pérez C, Castro A, Martínez A.
    Bioorg Med Chem; 2005 Dec 15; 13(24):6795-802. PubMed ID: 16183292
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  • 12. [Determination of cholinesterase specificity in studied preparation].
    Zhukovskiĭ IuG.
    Zh Evol Biokhim Fiziol; 2003 Dec 15; 39(3):218-25. PubMed ID: 12973903
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  • 14. [Role of substrate inhibition of myoneural junction acetylcholinesterase in the mechanism of the blocking action of irreversible cholinesterase inhibitors on neuromuscular behavior].
    Ivanov IuIa.
    Dokl Akad Nauk SSSR; 1972 Feb 21; 202(6):1464-6. PubMed ID: 5012275
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  • 16. Acetylcholinesterase and butyrylcholinesterase inhibitory compounds from Corydalis cava Schweigg. & Kort.
    Adsersen A, Kjølbye A, Dall O, Jäger AK.
    J Ethnopharmacol; 2007 Aug 15; 113(1):179-82. PubMed ID: 17574358
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  • 17. [The generalized mechanism of the irreversible inhibition of cholinesterase activity by organophosphorus inhibitors].
    Agabekian RS, Liubimov VS.
    Dokl Akad Nauk SSSR; 1991 Aug 15; 318(2):459-66. PubMed ID: 1893839
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  • 18. Synthesis of novel phenserine-based-selective inhibitors of butyrylcholinesterase for Alzheimer's disease.
    Yu Q, Holloway HW, Utsuki T, Brossi A, Greig NH.
    J Med Chem; 1999 May 20; 42(10):1855-61. PubMed ID: 10346939
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  • 19. Synthesis of organophosphates with fluorine-containing leaving groups as serine esterase inhibitors with potential for Alzheimer disease therapeutics.
    Makhaeva GF, Aksinenko AY, Sokolov VB, Serebryakova OG, Richardson RJ.
    Bioorg Med Chem Lett; 2009 Oct 01; 19(19):5528-30. PubMed ID: 19717305
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  • 20. [Reactivation of phosphorylated cholinesterase immobilized in a gelatin membrane].
    Kugusheva LI, Nikol'skaia EB.
    Ukr Biokhim Zh (1978); 1990 Oct 01; 62(2):93-6. PubMed ID: 2368191
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