J. Cabal

发表

Acetylcholinesterase Based Colorimetric Dipsticks for Military Performance: Principles and Construction

K. Kuča, M. Pohanka, J. Zdarova-Karasova, 2013 .

Cyclodextrines as functional agents for decontamination of the skin contaminated by nerve agents.

V. Dohnal, K. Kuča, J. Cabal, 2004, Acta medica.

Reactivation of VX-inhibited AChE by novel oximes having two oxygen atoms in the linker.

K. Kuča, J. Pejchal, D. Jun, 2010, Environmental toxicology and pharmacology.

3-Nitropropionic acid and similar nitrotoxins.

J. Patočka, J. Fusek, J. Cabal, 2000, Acta medica.

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

K. Kuča, D. Jun, V. Opletalová, 2006, Basic & clinical pharmacology & toxicology.

ACUTE TOXICITY OF SURFACTANTS AND DETERGENT -BASED DECONTAMINANTS IN MICE AND RATS

K. Kuča, L. Novotný, J. Misík, 2012 .

IN VITRO SKIN PERMEATION OF DETERGENTS AND DETERGENT-BASED DECONTAMINATION MIXTURE

K. Kuča, D. Josse, J. Misík, 2012 .

In vitro skin permeation and decontamination of the organophosphorus pesticide paraoxon under various physical conditions – evidence for a wash-in effect

K. Kuča, D. Josse, J. Misík, 2012, Toxicology mechanisms and methods.

Synthesis of a new reactivator of tabun-inhibited acetylcholinesterase.

K. Kuča, J. Kassa, J. Cabal, 2003, Bioorganic & medicinal chemistry letters.

Oxime reactivation of acetylcholinesterase inhibited by toxic phosphorus esters: in vitro kinetics and thermodynamics

K. Kuča, D. Jun, J. Patočka, 2005 .

A new group of monoquaternary reactivators of acetylcholinesterase inhibited by nerve agents

K. Kuča, Milan Kivala, M. Kohout, 2005, Journal of enzyme inhibition and medicinal chemistry.

IN VITRO REACTIVATION POTENCY OF NEWLY DEVELOPED OXIMES K 027 AND K 048

K. Kuča, D. Jun, J. Kassa, 2010 .

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

K. Kuča, J. Kassa, J. Cabal, 2004, Basic & clinical pharmacology & toxicology.

Synthesis of a potential reactivator of acetylcholinesterase—1-(4-hydroxyiminomethylpyridinium)-3-(carbamoylpyridinium)propane dibromide

K. Kuča, J. Cabal, J. Bielavský, 2003 .

SYNTHESIS OF THE ISOQUINOLINIUM SALTS DIFFERING IN THE LENGTH OF THE SIDE ALKYLATING CHAIN

K. Kuča, K. Musílek, O. Soukup, 2012 .

Preparation of Quinolinium Salts Differing in the Length of the Alkyl Side Chain

K. Kuča, V. Buchta, K. Musílek, 2012, Molecules.

Preparation of the Pyridinium Salts Differing in the Length of the N-Alkyl Substituent

K. Kuča, K. Musílek, O. Soukup, 2010, Molecules.

Kinetics of decompositition of organophosphate Fenitrothion by decontaminating foam-making blends

K. Kuča, J. Cabal, Jitka Míčová, 2007 .

Determination of Benzalkonium Bromide Homologues in Disinfection Products Using High‐Performance Liquid Chromatography

V. Dohnal, K. Kuča, J. Cabal, 2005 .

Acute toxicity of some nerve agents and pesticides in rats

K. Kuča, J. Misík, J. Cabal, 2015, Drug and chemical toxicology.

A COMPLEX PROCESS OF THE DEVELOPMENT OF NEW ACETYLCHOLINESTERASE REACTIVATORS - FROM PREDICTION TO IN VIVO EVALUATION

V. Dohnal, K. Kuča, D. Jun, 2005 .

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

K. Kuča, D. Jun, J. Bajgar, 2006, Journal of enzyme inhibition and medicinal chemistry.

Effective bisquaternary reactivators of tabun‐inhibited AChE

K. Kuča, D. Jun, K. Musílek, 2005, Journal of applied toxicology : JAT.

A comparison of the efficacy of a new asymmetric bispyridinium oxime BI-6 with currently available oximes and H oximes against soman by in vitro and in vivo methods.

J. Kassa, J. Cabal, 1999, Toxicology.

A comparison of the efficacy of acetylcholinesterase reactivators against cyclohexyl methylphosphonofluoridate (GF agent) by in vitro and in vivo methods.

J. Kassa, J. Cabal, 1999, Pharmacology & toxicology.

Design of a potent reactivator of tabun-inhibited acetylcholinesterase--synthesis and evaluation of (E)-1-(4-carbamoylpyridinium)-4-(4-hydroxyiminomethylpyridinium)-but-2-ene dibromide (K203).

K. Kuča, D. Jun, F. Gunn-Moore, 2007, Journal of medicinal chemistry.

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

K. Kuča, D. Jun, J. Kassa, 2005, Journal of applied toxicology : JAT.

A Comparison of the Efficacy of New Asymmetric Bispyridinium Oximes (K027, K048) with Currently Available Oximes Against Tabun by In Vivo Methods

K. Kuča, J. Kassa, M. Paar, 2006, Journal of toxicology and environmental health. Part A.

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

K. Kuča, D. Jun, J. Patočka, 2005, Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia.

Synthesis of the three monopyridinium oximes and evaluation of their potency to reactivate acetylcholinesterase inhibited by nerve agents

K. Kuča, J. Pícha, J. Cabal, 2004 .

Synthesis of Bisquaternary Symmetric - X,δ-Bis(2-Hydroxyiminomethylpyridinium) Alkane Dibromides and Their Reactivation of Cyclosarin-Inhibited Acetylcholinesterase

K. Kuča, J. Patočka, J. Kassa, 2004 .

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

K. Kuča, D. Jun, J. Kassa, 2006, Journal of toxicology and environmental health. Part A.

Pharmacological Prophylaxis and Antidotal Treatment of Acute Tabun Poisoning

K. Kuča, J. Vachek, J. Kassa, 2018 .

In vivo decontamination of the nerve agent VX using the domestic swine model

K. Kuča, L. Novotný, J. Misík, 2012, Clinical toxicology.

Inhibition of blood cholinesterases following intoxication with VX and its derivatives

K. Kuča, D. Jun, J. Kassa, 2007, Journal of applied toxicology : JAT.

Strategy for the development of new acetylcholinesterase reactivators - antidotes used for treatment of nerve agent poisonings.

V. Dohnal, K. Kuča, D. Jun, 2005, Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia.

In Vitro Comparison of Two Most Promising H-Oximes (HI-6 and HLö-7) and Currently Commercially Available Reactivators Pralidoxime and Obidoxime in Reactivation of Cyclosarin-Inhibited Human Cholinesterases

K. Kuča, D. Jun, J. Cabal, 2008, Toxicology mechanisms and methods.

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

K. Kuča, D. Jun, J. Kassa, 2005, Journal of applied toxicology : JAT.

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

K. Kuča, J. Kassa, J. Cabal, 2005, Journal of toxicology and environmental health. Part A.

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.

K. Kuča, D. Jun, J. Kassa, 2005, Acta medica.

Colorimetric dipstick for assay of organophosphate pesticides and nerve agents represented by paraoxon, sarin and VX.

Miroslav Pohanka, Kamil Kuca, Jan Korabecny, 2010, Talanta.

Reactivation of organophosphate inhibited acetylcholinesterase activity by α,ω-bis-(4-hydroxyiminomethylpyridinium)alkanes in vitro

Kamil Kuca, Jiří Patočka, K. Kuča, 2003 .

A comparison of decontamination effects of commercially available detergents in rats pre-exposed to topical sulphur mustard

K. Kuča, J. Misík, P. Jošt, 2013, Cutaneous and ocular toxicology.

Evaluation of flow injection analysis for determination of cholinesterase activities in biological material.

J. Kassa, J. Bajgar, J. Cabal, 2010, Chemico-biological interactions.

Tabun-inhibited rat tissue and blood cholinesterases and their reactivation with the combination of trimedoxime and HI-6 in vivo.

J. Kassa, J. Fusek, J. Karasova, 2010, Chemico-biological interactions.

In vitro reactivation potency of acetylcholinesterase reactivators — K074 and K075 — to reactivate tabun-inhibited human brain cholinesterases

K. Kuča, D. Jun, K. Musílek, 2007, Neurotoxicity Research.

Bisquaternary oximes as reactivators of tabun-inhibited human brain cholinesterases: an in vitro study.

K. Kuča, D. Jun, J. Cabal, 2007, Basic & clinical pharmacology & toxicology.

Potency of Five Structurally Different Acetylcholinesterase Reactivators to Reactivate Human Brain Cholinesterases Inhibited by Cyclosarin

K. Kuča, D. Jun, M. Hrabinová, 2007, Clinical toxicology.

In Vitro Evaluation of Acetylcholinesterase Reactivators as Potential Antidotes Against Tabun Nerve Agent Poisonings

K. Kuča, D. Jun, M. Hrabinová, 2006, Drug and chemical toxicology.

Evaluation of Newly Synthesized Reactivators of the Brain Cholinesterase Inhibited by Sarin Nerve Agent

K. Kuča, J. Cabal, 2005, Toxicology mechanisms and methods.

Inhibition of blood cholinesterases by nerve agents in vitro

K. Kuča, D. Jun, J. Kassa, 2009 .

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

K. Kuča, D. Jun, J. Kassa, 2005 .

In vitro Evaluation of New Acetylcholinesterase Reactivators as Casual Antidotes against Tabun and Cyclosarin

K. Kuča, D. Jun, Young-Sik Jung, 2006 .

Hydrolytic Reactions of Methylfluorophosphonates with Cyclodextrins

J. Cabal, 1995 .

Kinetics of hydrolysis of organophosphate soman by cationic surfactant Resamin AE

K. Kuča, J. Cabal, Jitka Míčová, 2010 .

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

K. Kuča, D. Jun, J. Kassa, 2005, Chemico-biological interactions.

A comparison of the efficacy of a new asymmetric bispyridinium oxime BI-6 with presently used oximes and H oximes against sarin by in vitro and in vivo methods

J. Kassa, J. Cabal, Jiří Kassa, 1999, Human & experimental toxicology.

A comparison of the potency of trimedoxime and other currently available oximes to reactivate tabun-inhibited acetylcholinesterase and eliminate acute toxic effects of tabun.

K. Kuča, J. Kassa, J. Cabal, 2005, Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia.

Comparison of ability of some oximes to reactivate sarin-inhibited brain acetylcholinesterase from different species.

K. Kuča, D. Jun, J. Kassa, 2005, Chemico-biological interactions.

USING THE PIG'S BRAIN ACETYLCHOLINESTERASE IMMOBILIZED ON A TEXTILE FIBER TO TEST THE ANTIDOTES OF NERVE AGENT POISONINGS - PART I

J. Cabal, Ivana Moravcová, Jitka Šandová, 2012 .

Voltammetric Biosensor Based on Acetylcholinesterase and Different Immobilization Protocols: A Simple Tool for Toxic Organophosphate Assay

K. Kuča, M. Pohanka, J. Zdarova-Karasova, 2011 .

Hydrates of Quaternary Ammonium Aldehydes as Potential Reactivators of Sarin-Inhibited Acetylcholinesterase

J. Patočka, F. Hampl, J. Cabal, 1998 .

Reactivation of organophosphate-inhibited acetylcholinesterase by quaternary pyridinium aldoximes

K. Kuča, D. Jun, J. Patočka, 2009, Neurotoxicity Research.

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.

K. Kuča, J. Kassa, J. Cabal, 2004, Die Pharmazie.

Colorimetric dipstick for assay of organophosphate pesticides and nerve agents represented by paraoxon, sarin and VX.

K. Kuča, M. Pohanka, J. Korábečný, 2010, Talanta.

In vitro skin decontamination of paraoxon – wet-type cleansing effect of selected detergents

K. Kuča, J. Misík, J. Marek, 2018, Cutaneous and ocular toxicology.

Evaluation of Newly Synthesized Reactivators of the Brain Cholinesterase Inhibited by Sarin Nerve Agent

K. Kuča, J. Cabal, 2005, Toxicology mechanisms and methods.

Reactivation of human brain homogenate cholinesterases inhibited by Tabun using newly developed oximes K117 and K127.

K. Kuča, L. Novotný, D. Jun, 2009, Basic & clinical pharmacology & toxicology.