메뉴 건너뛰기




Volumn 31, Issue 3, 2008, Pages 371-381

A comparison of the therapeutic and reactivating efficacy of newly developed oximes (K117, K127) and currently available oximes (obidoxime, trimedoxime, HI-6) in tabun-poisoned rats and mice

Author keywords

Acetylcholinesterase; HI 6; K117; K127; Mice; Obidoxime; Rats; Tabun; Trimedoxime

Indexed keywords

1 (4 CARBAMOYLPYRIDINIO) 1' (2 HYDROXYIMINOMETHYLPYRIDINIO)DIMETHYL ETHER; ACETYLCHOLINESTERASE; ATROPINE; BIS(PYRIDINIUM OXIME) DERIVATIVE; K 117; K 127; OBIDOXIME; TABUN; TRIMEDOXIME;

EID: 47549090639     PISSN: 01480545     EISSN: 15256014     Source Type: Journal    
DOI: 10.1080/01480540802171258     Document Type: Article
Times cited : (10)

References (32)
  • 1
    • 10044275708 scopus 로고    scopus 로고
    • Organophosphate/nerve agent poisoning: Mechanism of action, diagnosis, prophylaxis, and treatment
    • Bajgar, J. (2004). Organophosphate/nerve agent poisoning: mechanism of action, diagnosis, prophylaxis, and treatment. Adv. Clin. Chem. 38:151-216.
    • (2004) Adv. Clin. Chem , vol.38 , pp. 151-216
    • Bajgar, J.1
  • 2
    • 0043265155 scopus 로고    scopus 로고
    • Tabun - reappearance 50 years later
    • in Czech
    • Cabal, J., Bajgar, J. (1999) Tabun - reappearance 50 years later (in Czech). Chem. Listy 93:27-31.
    • (1999) Chem. Listy , vol.93 , pp. 27-31
    • Cabal, J.1    Bajgar, J.2
  • 3
    • 4744354029 scopus 로고    scopus 로고
    • Specification of the structure of oximes able to reactivate tabun-inhibited acetylcholinesterase
    • Cabal, J., Kuca, K., Kassa, J. (2004). Specification of the structure of oximes able to reactivate tabun-inhibited acetylcholinesterase. Pharmacol. Toxicol. 95:81-86.
    • (2004) Pharmacol. Toxicol , vol.95 , pp. 81-86
    • Cabal, J.1    Kuca, K.2    Kassa, J.3
  • 4
    • 0026609482 scopus 로고
    • Efficacy of HLö-7 and pyrimidoxime as antidotes of nerve agent poisoning in mice
    • Clement, J. G., Hansen, A. S., Boulet, C. A. (1992). Efficacy of HLö-7 and pyrimidoxime as antidotes of nerve agent poisoning in mice. Arch. Toxicol. 66:216-219.
    • (1992) Arch. Toxicol , vol.66 , pp. 216-219
    • Clement, J.G.1    Hansen, A.S.2    Boulet, C.A.3
  • 5
    • 0028132872 scopus 로고
    • Review of oximes available for treatment of nerve agent poisoning
    • Dawson, R. M. (1994). Review of oximes available for treatment of nerve agent poisoning. J. Appl. Toxicol. 14:317-331.
    • (1994) J. Appl. Toxicol , vol.14 , pp. 317-331
    • Dawson, R.M.1
  • 6
    • 30144445702 scopus 로고    scopus 로고
    • Structural changes of phenylalanine 338 and histidine 447 revealed by the crystal structures of tabun-inhibited murine acetylcholinesterase
    • Ekström, F., Akfur, C., Tunemalm, A. K., Lundberg, S. (2006). Structural changes of phenylalanine 338 and histidine 447 revealed by the crystal structures of tabun-inhibited murine acetylcholinesterase. Biochemistry 45:74-81.
    • (2006) Biochemistry , vol.45 , pp. 74-81
    • Ekström, F.1    Akfur, C.2    Tunemalm, A.K.3    Lundberg, S.4
  • 8
    • 0029563628 scopus 로고
    • A comparison of trimedoxime, obidoxime, pralidoxime, and HI-6 in the treatment of oral organophosphorus insecticide poisoning in the rat
    • Jokanovic, M., Maksimovic, M. (1995) A comparison of trimedoxime, obidoxime, pralidoxime, and HI-6 in the treatment of oral organophosphorus insecticide poisoning in the rat. Arch. Toxicol. 70:119-123.
    • (1995) Arch. Toxicol , vol.70 , pp. 119-123
    • Jokanovic, M.1    Maksimovic, M.2
  • 9
    • 0036447187 scopus 로고    scopus 로고
    • Review of oximes in the antidotal treatment of poisoning by organophosphorus nerve agents
    • Kassa, J. (2002). Review of oximes in the antidotal treatment of poisoning by organophosphorus nerve agents. J. Toxicol. Clin. Toxicol. 40: 803-816.
    • (2002) J. Toxicol. Clin. Toxicol , vol.40 , pp. 803-816
    • Kassa, J.1
  • 10
    • 33645945883 scopus 로고    scopus 로고
    • The influence of oxime and anticholinergic drug selection on the potency of antidotal treatment to counteract acute toxic effects of tabun in mice
    • Kassa, J. (2006). The influence of oxime and anticholinergic drug selection on the potency of antidotal treatment to counteract acute toxic effects of tabun in mice. Neurotox. Res. 9:59-62.
    • (2006) Neurotox. Res , vol.9 , pp. 59-62
    • Kassa, J.1
  • 11
    • 0033037801 scopus 로고    scopus 로고
    • A comparison of the efficacy of a new asymmetric bispyridinium oxime BI-6 with currently available oximes and H oximes against soman by in vitro and in vivo methods
    • Kassa, J., Cabal, J. (1999a). A comparison of the efficacy of a new asymmetric bispyridinium oxime BI-6 with currently available oximes and H oximes against soman by in vitro and in vivo methods. Toxicology 132:111-118.
    • (1999) Toxicology , vol.132 , pp. 111-118
    • Kassa, J.1    Cabal, J.2
  • 12
    • 0032842369 scopus 로고    scopus 로고
    • A comparison of the efficacy of a new asymmetric bispyridinium oxime BI-6 with presently used oximes and H oximes against sarin by in vitro and in vivo methods
    • Kassa, J., Cabal, J. (1999b). A comparison of the efficacy of a new asymmetric bispyridinium oxime BI-6 with presently used oximes and H oximes against sarin by in vitro and in vivo methods. Hum. Exp. Toxicol. 18:560-565.
    • (1999) Hum. Exp. Toxicol , vol.18 , pp. 560-565
    • Kassa, J.1    Cabal, J.2
  • 13
    • 0032929883 scopus 로고    scopus 로고
    • A comparison of the efficacy of acetylcholinesterase reactivators against cyclohexylmethylphosphonofluoridate (GF agent) by in vitro and in vivo methods
    • Kassa, J., Cabal, J. (1999c). A comparison of the efficacy of acetylcholinesterase reactivators against cyclohexylmethylphosphonofluoridate (GF agent) by in vitro and in vivo methods. Pharmacol. Toxicol. 84:41-45.
    • (1999) Pharmacol. Toxicol , vol.84 , pp. 41-45
    • Kassa, J.1    Cabal, J.2
  • 14
    • 37149011244 scopus 로고    scopus 로고
    • An evaluation of therapeutic and reactivating effects of newly developed oximes (K156, K203) and commonly used oximes (obidoxime, trimedoxime, HI-6) in tabun-poisoned rats and mice
    • Kassa, J., Karasova, J., Musilek, K., Kuca, K. (2008). An evaluation of therapeutic and reactivating effects of newly developed oximes (K156, K203) and commonly used oximes (obidoxime, trimedoxime, HI-6) in tabun-poisoned rats and mice. Toxicology, 243: 311-316.
    • (2008) Toxicology , vol.243 , pp. 311-316
    • Kassa, J.1    Karasova, J.2    Musilek, K.3    Kuca, K.4
  • 15
    • 33847239864 scopus 로고    scopus 로고
    • The development of new structural analogues of oximes for the antidotal treatment of poisoning by nerve agents and the comparison of their reactivating and therapeutic efficacy with currently available oximes
    • Kassa, J., Kuca, K., Bartosova, L., Kunesova, G. (2007). The development of new structural analogues of oximes for the antidotal treatment of poisoning by nerve agents and the comparison of their reactivating and therapeutic efficacy with currently available oximes. Curr. Org. Chem. 11:267-283.
    • (2007) Curr. Org. Chem , vol.11 , pp. 267-283
    • Kassa, J.1    Kuca, K.2    Bartosova, L.3    Kunesova, G.4
  • 16
    • 19544367621 scopus 로고    scopus 로고
    • Design and synthesis of new bispyridinium oxime reactivators for acetylcholinesterase inhibited by organophosphorous nerve agents
    • Kim, T.-H., Kuca K., Jun, D., Jung, Y.-S. (2005). Design and synthesis of new bispyridinium oxime reactivators for acetylcholinesterase inhibited by organophosphorous nerve agents. Bioorg. Med. Chem. Lett. 15:2914-2917.
    • (2005) Bioorg. Med. Chem. Lett , vol.15 , pp. 2914-2917
    • Kim, T.-H.1    Kuca, K.2    Jun, D.3    Jung, Y.-S.4
  • 17
    • 33744793990 scopus 로고    scopus 로고
    • Reactivation study of pyridinium oximes for acetylcholinesterases inhibited by paraoxon or DFP
    • Kim, T.-H., Oh, K.-A., Park, N.-J., Park, N.-S., Kim, Y.J., Yum, E.K., Jung Y.-S. (2006). Reactivation study of pyridinium oximes for acetylcholinesterases inhibited by paraoxon or DFP. J. Appl. Biomed. 4:67-72.
    • (2006) J. Appl. Biomed , vol.4 , pp. 67-72
    • Kim, T.-H.1    Oh, K.-A.2    Park, N.-J.3    Park, N.-S.4    Kim, Y.J.5    Yum, E.K.6    Jung, Y.-S.7
  • 18
    • 0027954088 scopus 로고
    • A comparison of the efficacy of HI-6 and 2-PAM against soman, tabun, sarin, and VX in the rabbit
    • Koplovitz, I., Stewart, J. R. (1994). A comparison of the efficacy of HI-6 and 2-PAM against soman, tabun, sarin, and VX in the rabbit. Toxicol. Lett. 70:169-179.
    • (1994) Toxicol. Lett , vol.70 , pp. 169-179
    • Koplovitz, I.1    Stewart, J.R.2
  • 19
    • 6344241309 scopus 로고    scopus 로고
    • A comparison of the efficacy of a bispyridinium oxime - 1,4-bis-(2-hydroxyiminomethylpyridinium) butane dibromide and currently used oximes to reactivate sarin, tabun, or cyclosarin-inhibited acetylcholinesterase by in vitro methods
    • Kuca, K., Cabal, J., Kassa, J. (2004). A comparison of the efficacy of a bispyridinium oxime - 1,4-bis-(2-hydroxyiminomethylpyridinium) butane dibromide and currently used oximes to reactivate sarin, tabun, or cyclosarin-inhibited acetylcholinesterase by in vitro methods. Pharmazie 59:795-798.
    • (2004) Pharmazie , vol.59 , pp. 795-798
    • Kuca, K.1    Cabal, J.2    Kassa, J.3
  • 20
    • 33645233664 scopus 로고    scopus 로고
    • In vitro evaluation of new acetylcholinesterase reactivators as casual antidotes against tabun and cyclosarin
    • Kuca, K., Jun, D., Kim, T.-H., Cabal, J., Jung, Y.-S. (2006a). In vitro evaluation of new acetylcholinesterase reactivators as casual antidotes against tabun and cyclosarin. Bull. Korean Chem. Soc. 27:395-398.
    • (2006) Bull. Korean Chem. Soc , vol.27 , pp. 395-398
    • Kuca, K.1    Jun, D.2    Kim, T.-H.3    Cabal, J.4    Jung, Y.-S.5
  • 21
    • 33646056667 scopus 로고    scopus 로고
    • Structural requirements of acetylcholinesterase reactivators
    • Kuca, K., Jun, D., Musilek, K. (2006b). Structural requirements of acetylcholinesterase reactivators. Mini Rev. Med. Chem. 6:269-277.
    • (2006) Mini Rev. Med. Chem , vol.6 , pp. 269-277
    • Kuca, K.1    Jun, D.2    Musilek, K.3
  • 22
    • 33845776174 scopus 로고    scopus 로고
    • Potency of new structurally different oximes to reactivate cyclosarin-inhibited human brain acetylcholinesterase
    • Kuca, K., Cabal, J., Jun, D., Bajgar, J., Hrabinova, M. (2006c). Potency of new structurally different oximes to reactivate cyclosarin-inhibited human brain acetylcholinesterase. J. Enz. Inhib. Med. Chem. 21:663-666.
    • (2006) J. Enz. Inhib. Med. Chem , vol.21 , pp. 663-666
    • Kuca, K.1    Cabal, J.2    Jun, D.3    Bajgar, J.4    Hrabinova, M.5
  • 23
    • 0003107857 scopus 로고    scopus 로고
    • Organophosphorus compounds
    • Spencer, P. S, Schaumburg, H. H, eds, New York: Oxford University Press, pp
    • Lotti M. (2000). Organophosphorus compounds. In: Spencer, P. S., Schaumburg, H. H., eds. Experimental and Clinical Neurotoxicology. New York: Oxford University Press, pp. 898-925.
    • (2000) Experimental and Clinical Neurotoxicology , pp. 898-925
    • Lotti, M.1
  • 24
    • 0027281533 scopus 로고
    • Organophosphate poisoning
    • Marrs, T. C. (1993). Organophosphate poisoning. Pharmacol. Ther. 58:51-66.
    • (1993) Pharmacol. Ther , vol.58 , pp. 51-66
    • Marrs, T.C.1
  • 25
    • 33745452125 scopus 로고    scopus 로고
    • Synthesis of reactivators of phosphorylated acetylcholinestrerase of bispyridiniumdialdoxime type with a 3-oxapentane connecting chain and their testing in vitro on a model of the enzyme inhibited by chlorpyrifos and methylchlorpyrifos. [in Czech]
    • Musilek, K., Kuca, K., Jun, D., Dohnal, V., Kim, T.-H., Jung, Y.-S., Dolezal, M. (2006). Synthesis of reactivators of phosphorylated acetylcholinestrerase of bispyridiniumdialdoxime type with a 3-oxapentane connecting chain and their testing in vitro on a model of the enzyme inhibited by chlorpyrifos and methylchlorpyrifos. [in Czech] Ces. Slov. Farm. 55:115-119.
    • (2006) Ces. Slov. Farm , vol.55 , pp. 115-119
    • Musilek, K.1    Kuca, K.2    Jun, D.3    Dohnal, V.4    Kim, T.-H.5    Jung, Y.-S.6    Dolezal, M.7
  • 26
    • 35848930605 scopus 로고    scopus 로고
    • Design of a potent reactivator of tabun-inhibited acetylcholinesterase - synthesis and evaluation of (E)-1-(4-carbamoylpyridinium)-4-(4- hydroxyiminomethylpyridinium)-but-2-ene dibromide (K203)
    • Musilek, K., Jun, D., Cabal, J., Kassa, J., Gunn-Moore, F., Kuca, K. (2007). Design of a potent reactivator of tabun-inhibited acetylcholinesterase - synthesis and evaluation of (E)-1-(4-carbamoylpyridinium)-4-(4- hydroxyiminomethylpyridinium)-but-2-ene dibromide (K203). J. Med. Chem. 50:5514-5518.
    • (2007) J. Med. Chem , vol.50 , pp. 5514-5518
    • Musilek, K.1    Jun, D.2    Cabal, J.3    Kassa, J.4    Gunn-Moore, F.5    Kuca, K.6
  • 27
    • 34547869780 scopus 로고    scopus 로고
    • Five oximes (K-27, K-48, obidoxime, HI-6, and trimedoxime) in comparison with pralidoxime: Survival in rats exposed to methyl-paraoxon
    • Petroianu, G. A., Nurulain, S. M., Nagelkerke, N., Shafiullah, M., Kassa, J., Kuca, K. (2007). Five oximes (K-27, K-48, obidoxime, HI-6, and trimedoxime) in comparison with pralidoxime: survival in rats exposed to methyl-paraoxon. J. Appl. Toxicol. 27:453-457.
    • (2007) J. Appl. Toxicol , vol.27 , pp. 453-457
    • Petroianu, G.A.1    Nurulain, S.M.2    Nagelkerke, N.3    Shafiullah, M.4    Kassa, J.5    Kuca, K.6
  • 28
    • 0022553280 scopus 로고
    • Reactivation of nerve-agent-inhibited acetylcholinesterases by HI-6 and obidoxime
    • Puu, G., Artursson, E., Bucht, G. (1986). Reactivation of nerve-agent-inhibited acetylcholinesterases by HI-6 and obidoxime. Biochem. Pharmacol. 35:1505-1510.
    • (1986) Biochem. Pharmacol , vol.35 , pp. 1505-1510
    • Puu, G.1    Artursson, E.2    Bucht, G.3
  • 31
    • 0029930604 scopus 로고    scopus 로고
    • Reactivation by various oximes of human erythrocyte acetylcholinesterase inhibited by different organophosphorus compounds
    • Worek, F., Kirchner, T., Bäker, M., Szinicz, L. (1996). Reactivation by various oximes of human erythrocyte acetylcholinesterase inhibited by different organophosphorus compounds. Arch. Toxicol. 70:497-503.
    • (1996) Arch. Toxicol , vol.70 , pp. 497-503
    • Worek, F.1    Kirchner, T.2    Bäker, M.3    Szinicz, L.4
  • 32
    • 0031978963 scopus 로고    scopus 로고
    • Reactivating potency of obidoxime, pralidoxime, HI-6, and HLö-7 in human erythrocyte acetylcholinesterase inhibited by highly toxic organophosphorus compounds
    • Worek, F., Widmann, R., Knopff, O., Szinicz, L. (1998). Reactivating potency of obidoxime, pralidoxime, HI-6, and HLö-7 in human erythrocyte acetylcholinesterase inhibited by highly toxic organophosphorus compounds. Arch. Toxicol. 72:237-243.
    • (1998) Arch. Toxicol , vol.72 , pp. 237-243
    • Worek, F.1    Widmann, R.2    Knopff, O.3    Szinicz, L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.