Publications
- Comparison of Novel Tacrine and 7-MEOTA Derivatives with Aromatic and Alicyclic Residues: Synthesis, Biological Evaluation and Docking Studies2013 | Faculty of Pharmacy in Hradec Králové, First Faculty of Medicine
- Comparison of Novel Tacrine and 7-MEOTA Derivatives with Aromatic and Alicyclic Residues: Synthesis, Biological Evaluation and Docking Studies2013 | Faculty of Pharmacy in Hradec Králové
- 7-Methoxytacrine-Adamantylamine Heterodimers as Cholinesterase Inhibitors in Alzheimer's Disease Treatment - Synthesis, Biological Evaluation and Molecular Modeling Studies2013 | Publication without faculty affiliation
- Synthesis of the isoquinolinium salts differing in the length of the side alkylating chain2012 | Publication without faculty affiliation
- Monoquarternary pyridinium salts with modified side chain - synthesis and evaluation on model of tabun- and paraoxon-inhibited acetylcholinesterase2008 | Faculty of Pharmacy in Hradec Králové, Central Library of Charles University
- Synthesis of monooxime-monocarbamoyl bispyridinium compounds bearing (E)-but-2-ene linker and evaluation of their reactivation activity against tabun- and paraoxon-inhibited acetylcholinesterase2008 | Faculty of Pharmacy in Hradec Králové, Central Library of Charles University
- Monoquarternary pyridinium salts with modified side chain - synthesis and evaluation on model of tabun- and paraoxon-inhibited acetylcholinesterase2008 | Central Library of Charles University
- Synthesis of monooxime-monocarbamoyl bispyridinium compounds bearing (E)-but-2-ene linker and evaluation of their reactivation activity against tabun- and paraoxon-inhibited acetylcholinesterase2008 | Central Library of Charles University
- 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)2007 | Faculty of Pharmacy in Hradec Králové, Central Library of Charles University
- Novel series of bispyridinium compounds bearing a (Z)-but-2-ene linker - Synthesis and evaluation of their reactivation activity against tabun and paraoxon-inhibited acetylcholinesterase2007 | Faculty of Pharmacy in Hradec Králové, Central Library of Charles University
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