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Volumn 175, Issue 1-3, 2008, Pages 187-191

Reactivation of model cholinesterases by oximes and intermediate phosphyloximes: A computational study

Author keywords

Cholinesterase; Decomposition; Density functional theory; Inhibition; Phosphyloximes

Indexed keywords

2 (HYDROXYIMINOMETHYL) 1 METHYLPYRIDINIUM CHLORIDE; 3 (HYDROXYIMINOMETHYL) 1 METHYLPYRIDINIUM CHLORIDE; 4 (HYDROXYIMINOMETHYL) 1 METHYLPYRIDINIUM CHLORIDE; CHOLINESTERASE; CYCLOSARIN; METHYLPHOSPHONOTHIOIC ACID S (2 DIISOPROPYLAMINOETHYL) O ETHYL ESTER; ORGANOPHOSPHORUS COMPOUND; OXIME; PARAOXON; PHOSPHYLOXIME; SARIN; TABUN; UNCLASSIFIED DRUG;

EID: 50649096376     PISSN: 00092797     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cbi.2008.05.006     Document Type: Article
Times cited : (7)

References (14)
  • 1
    • 28244473567 scopus 로고    scopus 로고
    • Evaluation of oxime efficacy in nerve agent poisoning: development of a kinetic-based dynamic model
    • Worek F., Szinicz L., Eyer P., and Thiermann H. Evaluation of oxime efficacy in nerve agent poisoning: development of a kinetic-based dynamic model. Toxicol. Appl. Pharmacol. 209 (2005) 193-202
    • (2005) Toxicol. Appl. Pharmacol. , vol.209 , pp. 193-202
    • Worek, F.1    Szinicz, L.2    Eyer, P.3    Thiermann, H.4
  • 2
    • 0037756828 scopus 로고    scopus 로고
    • Inhibition of cholinesterases with cationic phosphonyl oximes highlights distinctive properties of the charged pyridine groups of quaternary oxime reactivators
    • Ashani Y., Bhattacharjee A.K., Leader H., Saxena A., and Doctor B.P. Inhibition of cholinesterases with cationic phosphonyl oximes highlights distinctive properties of the charged pyridine groups of quaternary oxime reactivators. Biochem. Pharmacol. 66 (2003) 191-202
    • (2003) Biochem. Pharmacol. , vol.66 , pp. 191-202
    • Ashani, Y.1    Bhattacharjee, A.K.2    Leader, H.3    Saxena, A.4    Doctor, B.P.5
  • 3
    • 50649096624 scopus 로고    scopus 로고
    • Gaussian 03, Revision C.02, Gaussian, Inc., Pittsburgh PA, 2003. For full citation please refer to http://www.gaussian.com/citation_g03.htm
    • Gaussian 03, Revision C.02, Gaussian, Inc., Pittsburgh PA, 2003. For full citation please refer to http://www.gaussian.com/citation_g03.htm
  • 4
    • 4243553426 scopus 로고
    • Density-functional exchange-energy approximation with correct asymptotic behavior
    • Becke A.D. Density-functional exchange-energy approximation with correct asymptotic behavior. Phys. Rev. A 38 (1988) 3098-3100
    • (1988) Phys. Rev. A , vol.38 , pp. 3098-3100
    • Becke, A.D.1
  • 5
    • 0345491105 scopus 로고
    • Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density
    • Lee C., Yang W., and Parr R.G. Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density. Phys. Rev. B 37 (1988) 785-789
    • (1988) Phys. Rev. B , vol.37 , pp. 785-789
    • Lee, C.1    Yang, W.2    Parr, R.G.3
  • 6
    • 49649133169 scopus 로고
    • The effect of d-functions on molecular orbital energies for hydrocarbons
    • Hariharan P.C., and Pople J.A. The effect of d-functions on molecular orbital energies for hydrocarbons. Chem. Phys. Lett. 16 (1972) 217-219
    • (1972) Chem. Phys. Lett. , vol.16 , pp. 217-219
    • Hariharan, P.C.1    Pople, J.A.2
  • 7
    • 84986513567 scopus 로고
    • Determining atom-centered monopoles from molecular electrostatic potentials. The need for high sampling density in formamide conformational analysis
    • Breneman C.M., and Wiberg K.B. Determining atom-centered monopoles from molecular electrostatic potentials. The need for high sampling density in formamide conformational analysis. J. Comp. Chem. 11 (1990) 361-373
    • (1990) J. Comp. Chem. , vol.11 , pp. 361-373
    • Breneman, C.M.1    Wiberg, K.B.2
  • 8
    • 84961980477 scopus 로고    scopus 로고
    • Quantum mechanical continuum solvation models
    • Tomasi J., Mennucci B., and Cammi R. Quantum mechanical continuum solvation models. Chem. Rev. 105 (2005) 2999-3094
    • (2005) Chem. Rev. , vol.105 , pp. 2999-3094
    • Tomasi, J.1    Mennucci, B.2    Cammi, R.3
  • 9
    • 0015329117 scopus 로고
    • Reactivation of phosphorylated acetyl-cholinesterase. Dependence upon activator acidity
    • Hagedorn I., Stark I., and Lorenz H.P. Reactivation of phosphorylated acetyl-cholinesterase. Dependence upon activator acidity. Angew. Chem. Int. Ed. 11 (1972) 307-309
    • (1972) Angew. Chem. Int. Ed. , vol.11 , pp. 307-309
    • Hagedorn, I.1    Stark, I.2    Lorenz, H.P.3
  • 10
    • 50649124486 scopus 로고    scopus 로고
    • M. Harel, I. Silman, J.L. Sussman, The structure of torpedo californica acetylcholinesterase complexed with 2-PAM (PDB ID: 2VQ6), in press.
    • M. Harel, I. Silman, J.L. Sussman, The structure of torpedo californica acetylcholinesterase complexed with 2-PAM (PDB ID: 2VQ6), in press.
  • 11
    • 0013990356 scopus 로고
    • Crystallographic study of N-methyl-pyridine-2-aldoxime (2-PAM) halides
    • Carlstrom D. Crystallographic study of N-methyl-pyridine-2-aldoxime (2-PAM) halides. Acta Chem. Scand. 20 (1966) 1240-1246
    • (1966) Acta Chem. Scand. , vol.20 , pp. 1240-1246
    • Carlstrom, D.1
  • 12
    • 0037102534 scopus 로고    scopus 로고
    • Molecular structure, conformational analysis and charge distribution of Pralidoxime: ab Initio and DFT studies
    • Castro A.T., and Figueroa-Villar J.D. Molecular structure, conformational analysis and charge distribution of Pralidoxime: ab Initio and DFT studies. Int. J. Quant. Chem. 89 (2002) 135-146
    • (2002) Int. J. Quant. Chem. , vol.89 , pp. 135-146
    • Castro, A.T.1    Figueroa-Villar, J.D.2
  • 13
    • 84989135165 scopus 로고
    • Nuclear spin-spin interactions. XII. Nitrogen-15-proton coupling constants in the determination of oxime configurations
    • Crepaux D., and Lehn J.M. Nuclear spin-spin interactions. XII. Nitrogen-15-proton coupling constants in the determination of oxime configurations. Org. Magn. Reson. 7 (1975) 524-526
    • (1975) Org. Magn. Reson. , vol.7 , pp. 524-526
    • Crepaux, D.1    Lehn, J.M.2
  • 14
    • 0030850441 scopus 로고    scopus 로고
    • Direct reaction of oximes with sarin, soman, or tabun in vitro
    • Becker G., Kawan A., and Szinicz L. Direct reaction of oximes with sarin, soman, or tabun in vitro. Arch. Toxicol. 71 (1997) 714-718
    • (1997) Arch. Toxicol. , vol.71 , pp. 714-718
    • Becker, G.1    Kawan, A.2    Szinicz, L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.