Jun D - Search Results

1

N-alkylated Tacrine Derivatives as Potential Agents in Alzheimer's Disease Therapy.

Nepovimova E, Korabecny J, Hepnarova V, Jun D, Dolezal R, Muckova L, Jost P, Soukup O, Janockova J, Pham NL, Nguyen TD, Valis M, Kuca K. Nepovimova E, et al. Among authors: jun d. Curr Alzheimer Res. 2019;16(4):333-343. doi: 10.2174/1567205016666190314163942. Curr Alzheimer Res. 2019. PMID: 30873921

2

Reactivation of organophosphate-inhibited acetylcholinesterase by quaternary pyridinium aldoximes.

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

3

Acetylcholinesterase and butyrylcholinesterase--important enzymes of human body.

Patocka J, Kuca K, Jun D. Patocka J, et al. Among authors: jun d. Acta Medica (Hradec Kralove). 2004;47(4):215-28. Acta Medica (Hradec Kralove). 2004. PMID: 15841900 Review.

4

Design and synthesis of new bis-pyridinium oxime reactivators for acetylcholinesterase inhibited by organophosphorous nerve agents.

Kim TH, Kuca K, Jun D, Jung YS. Kim TH, et al. Among authors: jun d. Bioorg Med Chem Lett. 2005 Jun 2;15(11):2914-7. doi: 10.1016/j.bmcl.2005.03.060. Epub 2005 Apr 21. Bioorg Med Chem Lett. 2005. PMID: 15911280

5

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

6

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

7

Effective bisquaternary reactivators of tabun-inhibited AChE.

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

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

10

Synthesis of the novel series of bispyridinium compounds bearing (E)-but-2-ene linker and evaluation of their reactivation activity against chlorpyrifos-inhibited acetylcholinesterase.

Musilek K, Kuca K, Jun D, Dohnal V, Dolezal M. Musilek K, et al. Among authors: jun d. Bioorg Med Chem Lett. 2006 Feb;16(3):622-7. doi: 10.1016/j.bmcl.2005.10.059. Epub 2005 Nov 8. Bioorg Med Chem Lett. 2006. PMID: 16288867

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