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Josef Jampilek

Researcher at Comenius University in Bratislava

Publications -  331
Citations -  6091

Josef Jampilek is an academic researcher from Comenius University in Bratislava. The author has contributed to research in topics: Lipophilicity & Chemistry. The author has an hindex of 36, co-authored 303 publications receiving 4695 citations. Previous affiliations of Josef Jampilek include Palacký University, Olomouc & Slovak Academy of Sciences.

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Antimicrobial effect of salicylamide derivatives against intestinal sulfate-reducing bacteria

TL;DR: In this paper, salicylamide derivatives against two different genera of intestinal SRB, Desulfovibrio and Desulfomicrobium, were investigated, and the highest potency against the two strains was observed for 4-chloro- N -{(2 S )-1]-(3,4-dichlorophenyl)amino]-3-methyl-1-oxobutan-2-yl}- 2-hydroxybenzamide (MIC 0.22 to 0.31
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Antibacterial and Herbicidal Activity of Ring-Substituted 2-Hydroxynaphthalene-1-carboxanilides

TL;DR: In this study, a series of twenty-two ring-substituted 2-hydroxynaphthalene-1-carboxanilides were prepared and characterized and showed the antibacterial and antimycobacterial activity against the tested strains comparable or higher than the standards ampicillin or isoniazid.
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Effect of selected 8-hydroxyquinoline-2-carboxanilides on viability and sulfate metabolism of Desulfovibrio piger

TL;DR: In this paper, the antimicrobial activity and biological properties of ring-substituted 8-hydroxyquinoline-2-carboxanilides against Desulfovibrio piger Vib-7 were studied.
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In Vitro Bactericidal Activity of 4- and 5-Chloro-2-hydroxy-N-[1-oxo-1-(phenylamino)alkan-2-yl]benzamides against MRSA

TL;DR: The most potent bactericidal agent was compound 1f exhibiting remarkable rapid concentration-dependent bactericidal effect even at 2x MIC even at 4, 6, and 8 h (with a reduction in bacterial count ranging from 3.08 to 3.75 log10 CFU/mL) after incubation against MRSA 63718.
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Synthesis and Biological Evaluation of N-Alkoxyphenyl-3-hydroxynaphthalene-2-carboxanilides

TL;DR: A series of fifteen new N-alkoxyphenylanilides of 3-hydroxynaphthalene-2-carboxylic acid was prepared and characterized and showed antibacterial and antimycobacterial activity against the tested strains comparable with or higher than that of the standards ampicillin or rifampicin.