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Volumn 157-158, Issue , 2005, Pages 367-368

(09) Comparison of the potency of newly developed and currently available oximes to reactivate nerve agent-inhibited acetylcholinesterase in vitro and in vivo

Author keywords

Acetylcholinesterase; Cyclosarin; Oxime; Reactivator; Tabun

Indexed keywords

1 (4 CARBAMOYLPYRIDINIO) 1' (2 HYDROXYIMINOMETHYLPYRIDINIO)DIMETHYL ETHER; ACETYLCHOLINESTERASE; ATROPINE; CYCLOSARIN; KO 27; KO 33; KO 48; OBIDOXIME; OXIME DERIVATIVE; PRALIDOXIME; TABUN; UNCLASSIFIED DRUG; CHOLINESTERASE INHIBITOR; NEUROTOXIN; OXIME;

EID: 28744449392     PISSN: 00092797     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cbi.2005.10.054     Document Type: Conference Paper
Times cited : (14)

References (6)
  • 1
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    • Organophosphates/nerve agents poisoning: Mechanism of action, diagnosis, prophylaxis and treatment
    • J. Bajgar Organophosphates/nerve agents poisoning: mechanism of action, diagnosis, prophylaxis and treatment Adv. Clin. Chem. 38 2004 151 216
    • (2004) Adv. Clin. Chem. , vol.38 , pp. 151-216
    • Bajgar, J.1
  • 2
    • 2342636418 scopus 로고    scopus 로고
    • In vitro reactivation of tabun-inhibited acetylcholinesterase using new oximes-K027, K005, K033 a K048
    • K. Kuca, and J. Cabal In vitro reactivation of tabun-inhibited acetylcholinesterase using new oximes-K027, K005, K033 a K048 Centr. Eur. J. Publ. Health. 12 2004 S59 S61
    • (2004) Centr. Eur. J. Publ. Health. , vol.12
    • Kuca, K.1    Cabal, J.2
  • 3
    • 17744420458 scopus 로고    scopus 로고
    • A comparison of the ability of a new bispyridinium oxime-1-(4- hydroxyiminomethylpyridinium)-4-(4-carbamoylpyridinium)butane dibromide and currently used oximes to reactivate nerve agent-inhibited rat brain acetylcholinesterase by in vitro methods
    • K. Kuca, and J. Kassa A comparison of the ability of a new bispyridinium oxime-1-(4-hydroxyiminomethylpyridinium)-4-(4-carbamoylpyridinium)butane dibromide and currently used oximes to reactivate nerve agent-inhibited rat brain acetylcholinesterase by in vitro methods J. Enzyme Inhib. Med. Chem. 18 2003 529 535
    • (2003) J. Enzyme Inhib. Med. Chem. , vol.18 , pp. 529-535
    • Kuca, K.1    Kassa, J.2
  • 4
    • 10044256187 scopus 로고    scopus 로고
    • Antidotal treatment of GF-agent intoxication in mice with new bispyridinium oximes
    • L. Sevelova, K. Kuca, and G. Krejcova Antidotal treatment of GF-agent intoxication in mice with new bispyridinium oximes Toxicology 207 2005 1 6
    • (2005) Toxicology , vol.207 , pp. 1-6
    • Sevelova, L.1    Kuca, K.2    Krejcova, G.3
  • 5
    • 4744354029 scopus 로고    scopus 로고
    • Specification of the structure of oximes able to reactivate tabun inhibited acetylcholinesterase
    • J. Cabal, K. Kuca, and J. Kassa Specification of the structure of oximes able to reactivate tabun inhibited acetylcholinesterase Pharmacol. Toxicol. 95 2004 81 86
    • (2004) Pharmacol. Toxicol. , vol.95 , pp. 81-86
    • Cabal, J.1    Kuca, K.2    Kassa, J.3
  • 6
    • 4944256223 scopus 로고    scopus 로고
    • In vitro reactivation of acetylcholinesterase inhibited by cyclosarin using bisquaternary pyridinium aldoximes K005, K033, K027 and K048
    • K. Kuca, L. Sevelova-Bartosova, and G. Krejcova-Kunesova In vitro reactivation of acetylcholinesterase inhibited by cyclosarin using bisquaternary pyridinium aldoximes K005, K033, K027 and K048 Acta Med. (Hradec Kralove) 47 2004 107 109
    • (2004) Acta Med. (Hradec Kralove) , vol.47 , pp. 107-109
    • Kuca, K.1    Sevelova-Bartosova, L.2    Krejcova-Kunesova, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.