Kassa J - Search Results

1

Tacrine-Trolox Hybrids: A Novel Class of Centrally Active, Nonhepatotoxic Multi-Target-Directed Ligands Exerting Anticholinesterase and Antioxidant Activities with Low In Vivo Toxicity.

Nepovimova E, Korabecny J, Dolezal R, Babkova K, Ondrejicek A, Jun D, Sepsova V, Horova A, Hrabinova M, Soukup O, Bukum N, Jost P, Muckova L, Kassa J, Malinak D, Andrs M, Kuca K. Nepovimova E, et al. Among authors: kassa j. J Med Chem. 2015 Nov 25;58(22):8985-9003. doi: 10.1021/acs.jmedchem.5b01325. Epub 2015 Nov 10. J Med Chem. 2015. PMID: 26503905

2

Synthesis of a new reactivator of tabun-inhibited acetylcholinesterase.

Kuca K, Bielavský J, Cabal J, Kassa J. Kuca K, et al. Among authors: kassa 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

In vitro reactivation of acetylcholinesterase using the oxime K027.

Kuca K, Kassa J. Kuca K, et al. Among authors: kassa j. Vet Hum Toxicol. 2004 Feb;46(1):15-8. Vet Hum Toxicol. 2004. PMID: 14748409

4

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.

Kuca K, Kassa J. Kuca K, et al. Among authors: kassa j. J Enzyme Inhib Med Chem. 2003 Dec;18(6):529-35. doi: 10.1080/14756360310001605552. J Enzyme Inhib Med Chem. 2003. PMID: 15008517 Free article.

5

Oximes-induced reactivation of rat brain acetylcholinesterase inhibited by VX agent.

Kuca K, Kassa J. Kuca K, et al. Among authors: kassa j. Hum Exp Toxicol. 2004 Apr;23(4):167-71. doi: 10.1191/0960327104ht434oa. Hum Exp Toxicol. 2004. PMID: 15171567

6

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

Cabal J, Kuca K, Kassa J. Cabal J, et al. Among authors: kassa j. 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.

7

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. Kuca K, et al. Among authors: kassa j. Pharmazie. 2004 Oct;59(10):795-8. Pharmazie. 2004. PMID: 15544060

8

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: kassa 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

9

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: kassa j. J Appl Toxicol. 2005 Jul-Aug;25(4):271-6. doi: 10.1002/jat.1053. J Appl Toxicol. 2005. PMID: 16021679

10

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: kassa j. J Appl Toxicol. 2005 Jul-Aug;25(4):296-300. doi: 10.1002/jat.1065. J Appl Toxicol. 2005. PMID: 16025528

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