K
Katarina Kralova
Researcher at Comenius University in Bratislava
Publications - 129
Citations - 2364
Katarina Kralova is an academic researcher from Comenius University in Bratislava. The author has contributed to research in topics: Antimycobacterial & Lipophilicity. The author has an hindex of 27, co-authored 115 publications receiving 2025 citations. Previous affiliations of Katarina Kralova include Charles University in Prague & Cork Institute of Technology.
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Investigating biological activity spectrum for novel styrylquinazoline analogues.
Josef Jampilek,Robert Musiol,Jacek Finster,Matus Pesko,James Carroll,Katarina Kralova,Marcela Vejsova,Jim O'Mahony,Aidan Coffey,Jiri Dohnal,Jaroslaw Polanski +10 more
TL;DR: The structure-activity relationships (SAR) between the chemical structure and biological effects of the synthesized compounds are described and the relationships between the RP-HPLC retention parameter logK (the logarithm of capacity factor K) and logP data calculated by available programs are illustrated.
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Potential of Nanomaterial Applications in Dietary Supplements and Foods for Special Medical Purposes.
TL;DR: This contribution comprehensively summarizes the current state of the research focused on nanoformulated human and veterinary dietary supplements, nutraceuticals, and functional foods for special medical purposes, their particular applications in various food products and drinks as well as the most important related guidelines, regulations and directives.
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Synthesis and antimycobacterial evaluation of substituted pyrazinecarboxamides
Martin Dolezal,Pavlina Cmedlova,Lukas Palek,Jarmila Vinšová,Jiri Kunes,Vladimír Buchta,Josef Jampilek,Katarina Kralova +7 more
TL;DR: Structural-activity relationships among the chemical structures, the antimycobacterial, antifungal, photosynthesis inhibiting and antialgal activity of the evaluated substituted N-phenylpyrazine-2-carboxamides are discussed.
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Response of fast growing woody plants from family Salicaceae to cadmium treatment.
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Substituted pyrazinecarboxamides: synthesis and biological evaluation.
TL;DR: 3,5-Bromo-4-hydroxyphenyl derivatives of substituted pyrazinecarboxylic acid have shown the highest activity against Mycobacterium tuberculosis H(37)Rv (54-72% inhibition).