Cabal J - Search Results

1

Effective bisquaternary reactivators of tabun-inhibited AChE.

Kuca K, Cabal J, Musilek K, Jun D, Bajgar J. Kuca K, et al. Among authors: cabal j. J Appl Toxicol. 2005 Nov-Dec;25(6):491-5. doi: 10.1002/jat.1084. J Appl Toxicol. 2005. PMID: 16092078

2

Synthesis of a new reactivator of tabun-inhibited acetylcholinesterase.

Kuca K, Bielavský J, Cabal J, Kassa J. Kuca K, et al. Among authors: cabal j. Bioorg Med Chem Lett. 2003 Oct 20;13(20):3545-7. doi: 10.1016/s0960-894x(03)00751-0. Bioorg Med Chem Lett. 2003. PMID: 14505667

3

Specification of the structure of oximes able to reactivate tabun-inhibited acetylcholinesterase.

Cabal J, Kuca K, Kassa J. Cabal J, et al. Basic Clin Pharmacol Toxicol. 2004 Aug;95(2):81-6. doi: 10.1111/j.1742-7843.2004.950207.x. Basic Clin Pharmacol Toxicol. 2004. PMID: 15379785 Free article.

4

Reactivation of organophosphate-inhibited acetylcholinesterase by quaternary pyridinium aldoximes.

Kuca K, Patocka J, Cabal J, Jun D. Kuca K, et al. Among authors: cabal j. Neurotox Res. 2004;6(7-8):565-70. doi: 10.1007/BF03033452. Neurotox Res. 2004. PMID: 15639788

5

A comparison of the potency of newly developed oximes (K005, K027, K033, K048) and currently used oximes (pralidoxime, obidoxime, HI-6) to reactivate sarin-inhibited rat brain acetylcholinesterase by in vitro methods.

Kuca K, Cabal J, Kassa J. Kuca K, et al. Among authors: cabal j. J Toxicol Environ Health A. 2005 Apr 23;68(8):677-86. doi: 10.1080/15287390590921784. J Toxicol Environ Health A. 2005. PMID: 15901095

6

Comparison of in vitro potency of oximes (pralidoxime, obidoxime, HI-6) to reactivate sarin-inhibited acetylcholinesterase in various parts of pig brain.

Kuca K, Cabal J, Kassa J, Jun D, Hrabinová M. Kuca K, et al. Among authors: cabal j. J Appl Toxicol. 2005 Jul-Aug;25(4):271-6. doi: 10.1002/jat.1053. J Appl Toxicol. 2005. PMID: 16021679

7

In vitro reactivation potency of some acetylcholinesterase reactivators against sarin- and cyclosarin-induced inhibitions.

Kuca K, Cabal J, Jun D, Kassa J, Bartosová L, Kunesová G. Kuca K, et al. Among authors: cabal j. J Appl Toxicol. 2005 Jul-Aug;25(4):296-300. doi: 10.1002/jat.1065. J Appl Toxicol. 2005. PMID: 16025528

8

New quaternary pyridine aldoximes as casual antidotes against nerve agents intoxications.

Kuca K, Bartosová L, Jun D, Patocka J, Cabal J, Kassa J, Kunesová G. Kuca K, et al. Among authors: cabal j. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2005 Jun;149(1):75-82. doi: 10.5507/bp.2005.008. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2005. PMID: 16170392

9

A comparison of the potency of the oxime HLö-7 and currently used oximes (HI-6, pralidoxime, obidoxime) to reactivate nerve agent-inhibited rat brain acetylcholinesterase by in vitro methods.

Kuca K, Cabal J, Kassa J, Jun D, Hrabinová M. Kuca K, et al. Among authors: cabal j. Acta Medica (Hradec Kralove). 2005;48(2):81-6. Acta Medica (Hradec Kralove). 2005. PMID: 16259317

10

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

Kuca K, Bartosova L, Kassa J, Cabal J, Bajgar J, Kunesova G, Jun D. Kuca K, et al. Among authors: cabal j. Chem Biol Interact. 2005 Dec 15;157-158:367-8. doi: 10.1016/j.cbi.2005.10.054. Chem Biol Interact. 2005. PMID: 16429489

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