Hrabinova M - Search Results

1

Discovery of novel berberine derivatives with balanced cholinesterase and prolyl oligopeptidase inhibition profile.

Sobolova K, Hrabinova M, Hepnarova V, Kucera T, Kobrlova T, Benkova M, Janockova J, Dolezal R, Prchal L, Benek O, Mezeiova E, Jun D, Soukup O, Korabecny J. Sobolova K, et al. Among authors: hrabinova m. Eur J Med Chem. 2020 Oct 1;203:112593. doi: 10.1016/j.ejmech.2020.112593. Epub 2020 Jul 15. Eur J Med Chem. 2020. PMID: 32688201

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

4

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: hrabinova m. 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.

5

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: hrabinova m. J Toxicol Environ Health A. 2006 Aug;69(15):1431-40. doi: 10.1080/15287390500364283. J Toxicol Environ Health A. 2006. PMID: 16766478

6

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: hrabinova m. Drug Chem Toxicol. 2006;29(4):443-9. doi: 10.1080/01480540600718565. Drug Chem Toxicol. 2006. PMID: 16931445

7

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. 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.

8

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: hrabinova m. 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.

9

Substituted monoquaternary oximes as reactivators of cyclosarin--and chlorpyrifos--inhibited acetylcholinesterase.

Racakova V, Hrabinova M, Jun D, Kuca K. Racakova V, et al. Among authors: hrabinova m. Arh Hig Rada Toksikol. 2006 Dec;57(4):387-90. Arh Hig Rada Toksikol. 2006. PMID: 17265677

10

Potency of five structurally different acetylcholinesterase reactivators to reactivate human brain cholinesterases inhibited by cyclosarin.

Kuca K, Cabal J, Jun D, Hrabinova M. Kuca K, et al. Among authors: hrabinova m. Clin Toxicol (Phila). 2007 Jun-Aug;45(5):512-5. doi: 10.1080/15563650701354234. Clin Toxicol (Phila). 2007. PMID: 17503257

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