Search Results - "Żmudzki, P"

Degradation pathway of cephalosporin antibiotics by in vitro cultures of Lentinula edodes and Imleria badia by Dąbrowska, M., Muszyńska, B., Starek, M., Żmudzki, P., Opoka, W.

“…Bioremediation is a promising method to degrade active pharmaceutical ingredients with additional safety compared to conventional methods. This study provides…”
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A hybrid adsorbent/visible light photocatalyst for the abatement of microcystin-LR in water by Długosz, M, Kwiecień, A, Żmudzki, P, Bober, B, Krzek, J, Bialczyk, J, Nowakowska, M, Szczubiałka, K

“…A hybrid adsorbent/photocatalyst was obtained and used for the removal of microcystin-LR, a potent toxin, from water via adsorption and photocatalyzed…”
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Design, synthesis and cardiovascular evaluation of some aminoisopropanoloxy derivatives of xanthone by Kubacka, M., Szkaradek, N., Mogilski, S., Pańczyk, K., Siwek, A., Gryboś, A., Filipek, B., Żmudzki, P., Marona, H., Waszkielewicz, A.M.

“…[Display omitted] •We synthesized 8 derivatives of xanthone with structural elements of known drugs.•We evaluated cardiovascular activity of the tested…”
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An altered balance of plasma arginine metabolites is associated with increased thickness of the coronary intima-media complex in the adjacent to the culprit segment of an infarct-related artery by Molek, P, Zmudzki, P, Machnik, A, Nowak, G, Wnuk, M, Wlodarczyk, A, Nessler, J, Zalewski, J

“…Abstract Background The biomarkers of atherosclerosis remain insufficiently understood. Purpose We sought to investigate whether an altered balance of arginine…”
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Synthesis and activity of di- or trisubstituted N-(phenoxyalkyl)- or N-{2-[2-(phenoxy)ethoxy]ethyl}piperazine derivatives on the central nervous system by Pańczyk, Katarzyna, Pytka, Karolina, Jakubczyk, Magdalena, Rapacz, Anna, Sałat, Kinga, Furgała, Anna, Siwek, Agata, Głuch-Lutwin, Monika, Gryboś, Anna, Słoczyńska, Karolina, Pękala, Elżbieta, Żmudzki, Paweł, Bucki, Adam, Kołaczkowski, Marcin, Żelaszczyk, Dorota, Marona, Henryk, Waszkielewicz, Anna M.

“…[Display omitted] •Presented compounds possess mainly antagonistic activity for serotonergic receptors.•Compound 9 showed 5-HT1A Ki = 5 nM, 5-HT7 Ki = 70 nM,…”
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