Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Katarzyna Kral"'
Autor:
Ilona Wandzik, Wiesław Szeja, Urszula Nawrot, Tadeusz Bieg, Katarzyna Kral, Jadwiga Paszkowska
Publikováno v:
Molecules, Vol 18, Iss 7, Pp 8018-8027 (2013)
New derivatives of uridine which contain a b-ketoenol motif were synthesized, characterized and biologically tested. Synthesized compounds 1–4 showed no activity against bovine milk β-1,4-galactosyltransferase I at concentrations up to 2.0 mM and
Externí odkaz:
https://doaj.org/article/3eb8b60487e5430db9d388d5e49e86ec
Autor:
Tadeusz Bieg, Katarzyna Kral, Agnieszka Kudelko, Aleksandra Dąbrowska, Anna Barabaś, Ilona Wandzik
Publikováno v:
Nucleosides, Nucleotides & Nucleic Acids. 36:159-169
N-substituted isomeric hydrazones of uridyl aldehyde have been synthesized. The occurrence of the dominant E isomers with respect to the azomethine group was confirmed by means of NMR spectroscopy. Synthesized hydrazones feature an acetonide moiety a
Autor:
Tadeusz Bieg, Katarzyna Kral, Anna Lalik, Katarzyna Włodarczyk, Ilona Wandzik, Przemysław Hahn, Urszula Nawrot
Publikováno v:
Bioorganic Chemistry. 61:13-20
This study described the synthesis and in vitro evaluation of eight new derivatives of uridine as antifungal agents and inhibitors of chitin synthase. Dimeric uridinyl derivatives synthesized by us did not exhibit significant activity. One of the stu
Publikováno v:
Journal of Carbohydrate Chemistry. 31:593-601
D-glucal, D-galactal, and their 6-O-TBDMS derivatives were benzylated in a two-step procedure under microwave conditions. In the first step glycals were converted into dibutylstannylene acetal or tributyltin ether intermediates, which were next alkyl
Autor:
Natalia Jaśkowiak, Jadwiga Paszkowska, Ilona Wandzik, Katarzyna Węgrzyk, Alba Silipo, Karolina Żaba, Katarzyna Kral, Antonio Molinaro, Tadeusz Bieg
Publikováno v:
Bioorganic chemistry. 58
New 5'-glycyl derivatives of uridine containing fragments of varying lipophilicity were synthesized as analogues of natural peptidyl antibiotics. One of the studied compounds, 5'-O-(N-succinylglycyl)-2',3'-O-isopropylideneuridine (A4), showed moderat
Autor:
Urszula Nawrot, Ilona Wandzik, Wiesław Szeja, Jadwiga Paszkowska, Katarzyna Kral, Tadeusz Bieg
Publikováno v:
Molecules
Volume 18
Issue 7
Pages 8018-8027
Molecules, Vol 18, Iss 7, Pp 8018-8027 (2013)
Volume 18
Issue 7
Pages 8018-8027
Molecules, Vol 18, Iss 7, Pp 8018-8027 (2013)
New derivatives of uridine which contain a b-ketoenol motif were synthesized, characterized and biologically tested. Synthesized compounds 1–4 showed no activity against bovine milk β-1,4-galactosyltransferase I at concentrations up to 2.0 mM and
Publikováno v:
ChemInform. 44
D-Glucal, D-galactal (I), and their 6-O-protected derivatives, e.g. (IV), are benzylated in a two-step sequence.