Jun D - Search Results

1

Exploring Structure-Activity Relationship in Tacrine-Squaramide Derivatives as Potent Cholinesterase Inhibitors.

Svobodova B, Mezeiova E, Hepnarova V, Hrabinova M, Muckova L, Kobrlova T, Jun D, Soukup O, Jimeno ML, Marco-Contelles J, Korabecny J. Svobodova B, et al. Among authors: jun d. Biomolecules. 2019 Aug 19;9(8):379. doi: 10.3390/biom9080379. Biomolecules. 2019. PMID: 31430943 Free PMC article.

2

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

3

[A comparison of the efficacy of the reactivators of acetylcholinesterase inhibited with tabun].

Cabal J, Kuca K, Jun D, Bajgar J, Hrabinová M. Cabal J, et al. Among authors: jun d. Ceska Slov Farm. 2005 Jul;54(4):192-5. Ceska Slov Farm. 2005. PMID: 16124202 Czech.

4

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: jun d. Acta Medica (Hradec Kralove). 2005;48(2):81-6. Acta Medica (Hradec Kralove). 2005. PMID: 16259317

5

Russian VX: inhibition and reactivation of acetylcholinesterase compared with VX agent.

Kuca K, Jun D, Cabal J, Hrabinova M, Bartosova L, Opletalova V. Kuca K, et al. Among authors: jun d. Basic Clin Pharmacol Toxicol. 2006 Apr;98(4):389-94. doi: 10.1111/j.1742-7843.2006.pto_267.x. Basic Clin Pharmacol Toxicol. 2006. PMID: 16623863 Free article.

6

In vitro inactivation of rat brain acetylcholinesterase by DSP-4 and its derivatives OS-21 and OS-23 and protective activity of tacrine (9-amino-1,2,3,4-tetrahydroacridine).

Patockal J, Jun D, Kucal K. Patockal J, et al. Among authors: jun d. Acta Medica (Hradec Kralove). 2005;48(3-4):145-8. Acta Medica (Hradec Kralove). 2005. PMID: 16640027

7

In vitro potency of H oximes (HI-6, HLö-7), the oxime BI-6, and currently used oximes (pralidoxime, obidoxime, trimedoxime) to reactivate nerve agent-inhibited rat brain acetylcholinesterase.

Kuca K, Cabal J, Kassa J, Jun D, Hrabinova M. Kuca K, et al. Among authors: jun d. J Toxicol Environ Health A. 2006 Aug;69(15):1431-40. doi: 10.1080/15287390500364283. J Toxicol Environ Health A. 2006. PMID: 16766478

8

In vitro evaluation of acetylcholinesterase reactivators as potential antidotes against tabun nerve agent poisonings.

Kuca K, Cabal J, Jun D, Hrabinova M. Kuca K, et al. Among authors: jun d. Drug Chem Toxicol. 2006;29(4):443-9. doi: 10.1080/01480540600718565. Drug Chem Toxicol. 2006. PMID: 16931445

9

New group of xylene linker-containing acetylcholinesterase reactivators as antidotes against the nerve agent cyclosarin.

Hrabinova M, Musilek K, Jun D, Kuca K. Hrabinova M, et al. Among authors: jun d. J Enzyme Inhib Med Chem. 2006 Oct;21(5):515-9. doi: 10.1080/14756360600741420. J Enzyme Inhib Med Chem. 2006. PMID: 17194020 Free article.

10

Potency of new structurally different oximes to reactivate cyclosarin-inhibited human brain acetylcholinesterases.

Kuca K, Cabal J, Jun D, Bajgar J, Hrabinova M. Kuca K, et al. Among authors: jun d. J Enzyme Inhib Med Chem. 2006 Dec;21(6):663-6. doi: 10.1080/14756360600850916. J Enzyme Inhib Med Chem. 2006. PMID: 17252938 Free article.

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