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Half-inhibition concentrations of new cholinesterase inhibitors.
Zdrazilová P, Stepánková S, Komers K, Ventura K, Cegan A. Zdrazilová P, et al. Among authors: stepankova s. Z Naturforsch C J Biosci. 2004 Mar-Apr;59(3-4):293-6. doi: 10.1515/znc-2004-3-430. Z Naturforsch C J Biosci. 2004. PMID: 15241943 Free article.
Kinetics of 13 new cholinesterase inhibitors.
Zdrazilová P, Stĕpánková S, Komersová A, Vránová M, Komers K, Cegan A. Zdrazilová P, et al. Among authors: stepankova s. Z Naturforsch C J Biosci. 2006 Jul-Aug;61(7-8):611-7. doi: 10.1515/znc-2006-7-823. Z Naturforsch C J Biosci. 2006. PMID: 16989325 Free article.
Synthesis and in vitro evaluation of new derivatives of 2-substituted-6-fluorobenzo[d]thiazoles as cholinesterase inhibitors.
Imramovský A, Pejchal V, Štěpánková Š, Vorčáková K, Jampílek J, Vančo J, Šimůnek P, Královec K, Brůčková L, Mandíková J, Trejtnar F. Imramovský A, et al. Among authors: stepankova s. Bioorg Med Chem. 2013 Apr 1;21(7):1735-48. doi: 10.1016/j.bmc.2013.01.052. Epub 2013 Feb 1. Bioorg Med Chem. 2013. PMID: 23462716
Salicylanilide diethyl phosphates as cholinesterases inhibitors.
Krátký M, Štěpánková Š, Vorčáková K, Vinšová J. Krátký M, et al. Among authors: stepankova s. Bioorg Chem. 2015 Feb;58:48-52. doi: 10.1016/j.bioorg.2014.11.005. Epub 2014 Nov 13. Bioorg Chem. 2015. PMID: 25462625
Synthesis, structural characterization, docking, lipophilicity and cytotoxicity of 1-[(1R)-1-(6-fluoro-1,3-benzothiazol-2-yl)ethyl]-3-alkyl carbamates, novel acetylcholinesterase and butyrylcholinesterase pseudo-irreversible inhibitors.
Pejchal V, Štěpánková Š, Pejchalová M, Královec K, Havelek R, Růžičková Z, Ajani H, Lo R, Lepšík M. Pejchal V, et al. Among authors: stepankova s. Bioorg Med Chem. 2016 Apr 1;24(7):1560-72. doi: 10.1016/j.bmc.2016.02.033. Epub 2016 Feb 26. Bioorg Med Chem. 2016. PMID: 26947959
62 results