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pro vyhledávání: '"I, Polacek"'
Publikováno v:
Food / Nahrung. 38:378-381
Amaranth seeds are very small. Their bulk density is 843 g dm−3. Basic analysis of amaranth whole flour from Slovakia proved evidently a high content of proteins (17.7% on dry basis), what is typical for amaranths. The lipid content of amaranth gra
Publikováno v:
Food / Nahrung. 41:108-110
Content of amino acids and fatty acids in whole amaranth flour from Amaranthus hypochondriacus was investigated. In comparison with fine wheat flour, used in our experiments, high lysine content was observed (5,95 g/16 g N in comparison with 2,90 g/1
Autor:
SABOL, R., KLEIN, P., RYBA, T., HVIZDOS, L., VARGA, R., ROVNAK, M., SULLA, I., MUDRONOVA, D., GALIK, J., I. POLACEk, I., ZIVCAK, J., HUDAk, R.
Publikováno v:
Acta Physica Polonica: A; 2017, Vol. 131 Issue 4, p1150-1152, 3p
Autor:
B. Starke, I. Polacek
Publikováno v:
The Journal of Antibiotics. 33:1031-1036
Diastereomeric 7-(alpha-ureido-2-amino-4-thiazolylacetyl)cephalosporins are broad-spectrum antimicrobial agents with activity mainly against Gram-negative bacteria. The L-isomers were more potent than the D-isomers. All compounds showed some degree o
Autor:
I. Polacek
Publikováno v:
Biopharmaceutics & Drug Disposition. 2:69-77
Rats implanted with multiperforated subcutaneous plastic capsules were used as a model for study of the penetration of four cephalosporins into sites infected with Escherichia coli. The concentrations of the antibiotics were determined in uninfected
Akademický článek
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Publikováno v:
Chemischer Informationsdienst. 5
Autor:
I, Polacek, H, Breuer
Publikováno v:
Arzneimittel-Forschung. 28(5)
Dicyclohexylamine and related amino compounds as well as some simple secondary amines with branched aliphatic substituents were found to decrease blood glucose levels of fasted, glucose-loaded, or streptozotocin-diabetic rats, and of fasted mice. Str
Autor:
I. Polacek, H. Mühlbauer
Publikováno v:
Biopharmaceuticsdrug disposition. 1(3)
Displacement of cephazolin, a highly protein-bound beta-lactam antibiotic, by sulpha-phenazole was studied in vitro and in vivo. In vitro, the sulphonamide was effective in displacing the antibiotic from its binding sites at the concentration 100--10