메뉴 건너뛰기




Volumn 126, Issue 2, 2012, Pages 525-533

Synthesis and in vitro and in vivo inhibition potencies of highly relevant nerve agent surrogates

Author keywords

Acetylcholinesterase; Anticholinesterase; Nerve agent simulant; Nerve agent surrogate; Organophosphate

Indexed keywords

4 NITROPHENYL ETHYL DIMETHYLPHOSPHORAMIDATE; 4 NITROPHENYL ETHYL METHYLPHOSPHONATE; 4 NITROPHENYL ISOPROPYL METHYLPHOSPHONATE; ACETYLCHOLINESTERASE; CHOLINESTERASE; CHOLINESTERASE INHIBITOR; CHOLINESTERASE REACTIVATOR; PHTHALIMIDYL ISOPROPYL METHYLPHOSPHONATE; UNCLASSIFIED DRUG;

EID: 84859050276     PISSN: 10966080     EISSN: 10960929     Source Type: Journal    
DOI: 10.1093/toxsci/kfs013     Document Type: Article
Times cited : (62)

References (22)
  • 1
    • 84859063188 scopus 로고    scopus 로고
    • Agency for Toxic Substances and Disease Registry (ATSDR)
    • Agency for Toxic Substances and Disease Registry (ATSDR) (2011). Toxic Substances Portal-Nerve Agents (GA, GB, GD, VX). Available at: http://www.atsdr.cdc.gov/MMG/MMG.asp?id=523&tid=93.
    • (2011) Toxic Substances Portal-Nerve Agents (GA, GB, GD, VX)
  • 3
    • 0024504103 scopus 로고
    • An investigation of acetylcholinesterase inhibition and aging and choline acetyltransferase activity following a high level acute exposure to paraoxon
    • Chambers, H. W., and Chambers, J. E. (1989). An investigation of acetylcholinesterase inhibition and aging and choline acetyltransferase activity following a high level acute exposure to paraoxon. Pestic. Biochem. Physiol. 33, 125-131.
    • (1989) Pestic. Biochem. Physiol. , vol.33 , pp. 125-131
    • Chambers, H.W.1    Chambers, J.E.2
  • 4
    • 0025228432 scopus 로고
    • Time course of inhibition of acetylcholinesterase and aliesterases following parathion and paraoxon exposures in rats
    • Chambers, J. E., and Chambers, H. W. (1990). Time course of inhibition of acetylcholinesterase and aliesterases following parathion and paraoxon exposures in rats. Toxicol. Appl. Pharmcol. 103, 420-429.
    • (1990) Toxicol. Appl. Pharmcol. , vol.103 , pp. 420-429
    • Chambers, J.E.1    Chambers, H.W.2
  • 5
    • 84859023358 scopus 로고    scopus 로고
    • The metabolic activation and detoxication of anticholinesterase insecticides
    • (T. Satoh and R. C. Gupta, Eds.), Wiley, Hoboken, NJ
    • Chambers, J. E., Meek, E. C., and Ross, M. (2010). The metabolic activation and detoxication of anticholinesterase insecticides. In Anticholinesterase Pesticides: Metabolism, Neurotoxicity, and Epidemiology (T. Satoh and R. C. Gupta, Eds.), pp. 77-84. Wiley, Hoboken, NJ.
    • (2010) Anticholinesterase Pesticides: Metabolism, Neurotoxicity, and Epidemiology , pp. 77-84
    • Chambers, J.E.1    Meek, E.C.2    Ross, M.3
  • 6
    • 0023731405 scopus 로고
    • Effects of acute paraoxon and atropine exposures on retention of shuttle avoidance behavior in rats
    • Chambers, J. E., Wiygul, S. H., Harkness, J. E., and Chambers, H. W. (1988). Effects of acute paraoxon and atropine exposures on retention of shuttle avoidance behavior in rats. Neurosci. Res. Commun. 3, 85-92.
    • (1988) Neurosci. Res. Commun. , vol.3 , pp. 85-92
    • Chambers, J.E.1    Wiygul, S.H.2    Harkness, J.E.3    Chambers, H.W.4
  • 7
    • 0030293198 scopus 로고    scopus 로고
    • The effect of the human serum paraoxonase polymorphism is reversed with diazoxon, soman and sarin
    • Davies, H. G., Richter, R. J., Keifer, M., Broomfield, C. A., Sowalla, J., and Furlong, C. E. (1996). The effect of the human serum paraoxonase polymorphism is reversed with diazoxon, soman and sarin. Nat. Genet. 14, 334-336.
    • (1996) Nat. Genet. , vol.14 , pp. 334-336
    • Davies, H.G.1    Richter, R.J.2    Keifer, M.3    Broomfield, C.A.4    Sowalla, J.5    Furlong, C.E.6
  • 8
    • 17444414686 scopus 로고    scopus 로고
    • Toxic effects of pesticides
    • (C. D. Klaassen, Ed.), McGraw-Hill, New York, NY
    • Ecobichon, D. J. (2001). Toxic effects of pesticides. In Casarett and Doull's Toxicology (C. D. Klaassen, Ed.), pp. 763-810. McGraw-Hill, New York, NY.
    • (2001) Casarett and Doull's Toxicology , pp. 763-810
    • Ecobichon, D.J.1
  • 9
    • 33644811612 scopus 로고
    • A new and rapid colorimetric determination of acetylcholinesterase activity
    • Ellman, G. L., Courtney, K. D., Andres, V., and Featherstone, R. M. (1961). A new and rapid colorimetric determination of acetylcholinesterase activity. Biochem. Pharmacol. 7, 88-95.
    • (1961) Biochem. Pharmacol. , vol.7 , pp. 88-95
    • Ellman, G.L.1    Courtney, K.D.2    Andres, V.3    Featherstone, R.M.4
  • 10
    • 59649124122 scopus 로고    scopus 로고
    • Acute toxicity of organophosphorus compounds in guinea pigs is sex- and age-dependent and cannot be solely accounted for by acetylcholinesterase inhibition
    • Fawcett, W. P., Aracava, Y., Adler, M., Pereira, E. F., and Albuquerque, E. X. (2009). Acute toxicity of organophosphorus compounds in guinea pigs is sex- and age-dependent and cannot be solely accounted for by acetylcholinesterase inhibition. J. Pharmacol. Exp. Ther. 328, 516-524.
    • (2009) J. Pharmacol. Exp. Ther. , vol.328 , pp. 516-524
    • Fawcett, W.P.1    Aracava, Y.2    Adler, M.3    Pereira, E.F.4    Albuquerque, E.X.5
  • 11
    • 70350214937 scopus 로고    scopus 로고
    • Nerve agent analogs that produce authentic soman, sarin, tabun, and cyclohexyl methylphosphonate-modified human butyrylcholinesterase
    • Gilley, C., MacDonald, M., Nachon, F., Schopfer, L. M., Zhang, J., Cashman, J. R., and Lockridge, O. (2009). Nerve agent analogs that produce authentic soman, sarin, tabun, and cyclohexyl methylphosphonate-modified human butyrylcholinesterase. Chem. Res. Toxicol. 22, 1680-1688.
    • (2009) Chem. Res. Toxicol. , vol.22 , pp. 1680-1688
    • Gilley, C.1    MacDonald, M.2    Nachon, F.3    Schopfer, L.M.4    Zhang, J.5    Cashman, J.R.6    Lockridge, O.7
  • 12
  • 13
  • 14
    • 27544478172 scopus 로고    scopus 로고
    • Butyrylcholinesterase, paraoxonase, and albumin esterase, but not carboxylesterase, are present in human plasma
    • Li, B., Sedlacek, M., Manoharan, I., Boopathy, R., Duysen, E. G., Masson, P., and Lockridge, O. (2005). Butyrylcholinesterase, paraoxonase, and albumin esterase, but not carboxylesterase, are present in human plasma. Biochem. Pharmacol. 70, 1673-1684.
    • (2005) Biochem. Pharmacol. , vol.70 , pp. 1673-1684
    • Li, B.1    Sedlacek, M.2    Manoharan, I.3    Boopathy, R.4    Duysen, E.G.5    Masson, P.6    Lockridge, O.7
  • 16
    • 0026639319 scopus 로고
    • The specificity of carboxylesterase protection against the toxicity of organophosphorus compounds
    • Maxwell, D. M. (1992). The specificity of carboxylesterase protection against the toxicity of organophosphorus compounds. Toxicol. Appl. Pharmacol. 114, 306-312.
    • (1992) Toxicol. Appl. Pharmacol. , vol.114 , pp. 306-312
    • Maxwell, D.M.1
  • 17
    • 84871189788 scopus 로고    scopus 로고
    • Pyridinium oximes as cholinesterase reactivators in the treatment of op poisoning
    • (R. C. Gupta, Ed.), Elsevier, London, U.K
    • Milatovic, D., and Jokanovic, M. (2009). Pyridinium oximes as cholinesterase reactivators in the treatment of op poisoning. In Handbook of Toxicology of Chemical Warfare Agents. (R. C. Gupta, Ed.), pp. 985-996. Elsevier, London, U.K.
    • (2009) Handbook of Toxicology of Chemical Warfare Agents , pp. 985-996
    • Milatovic, D.1    Jokanovic, M.2
  • 20
    • 33845369068 scopus 로고    scopus 로고
    • New safe method for preparation of sarin-exposed human erythrocytes acetylcholinesterase using non-toxic and stable sarin analogue isopropyl p-nitrophenyl methy|phosphonate and its application to evaluation of nerve agent antidotes
    • Ohta, H., Ohmori, T., Suzuki, S., Ikegaya, H., Sakurada, K., and Takatori, T. (2006). New safe method for preparation of sarin-exposed human erythrocytes acetylcholinesterase using non-toxic and stable sarin analogue isopropyl p-nitrophenyl methy|phosphonate and its application to evaluation of nerve agent antidotes. Pharmaceut. Res. 23, 2827-2833.
    • (2006) Pharmaceut. Res. , vol.23 , pp. 2827-2833
    • Ohta, H.1    Ohmori, T.2    Suzuki, S.3    Ikegaya, H.4    Sakurada, K.5    Takatori, T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.