Výsledky vyhledávání - "Zsuzsánna Csíki"

Assessing toxicity of polyamidoamine dendrimers by neuronal signaling functions

Autor: Júlia Visy, Orsolya Kékesi, Péter Fügedi, Gábor Tárkányi, Ilona Fitos, Gabriella Nyitrai, Zsuzsánna Csíki, Krisztina Németh, Julianna Kardos, Péter Keglevich, Ágnes Simon, Ildikó Pál

Publikováno v: Nanotoxicology. 6:576-586

We report for the first time on neuronal signaling for the evaluation of interactions between native plasmamembrane and polyamidoamine (PAMAM) dendrimers. Generation 5 polycationic (G5-NH(2)), novel β-D-glucopyranose-conjugated G5-NH(2) and generati

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be0d211f5e9e8c0d9302cd270b649dfb
https://doi.org/10.3109/17435390.2011.591511

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Synthesis of glycosaminoglycan oligosaccharides. Part 4: Synthesis of aza-l-iduronic acid-containing analogs of heparan sulfate oligosaccharides as heparanase inhibitors

Autor: Zsuzsánna Csíki, Péter Fügedi

Publikováno v: Tetrahedron. 66:7821-7837

The synthesis of three azasugar-containing analogs of the disaccharide units of heparan sulfate, which are potential inhibitors of the enzyme heparanase, is reported. Synthetic routes were developed for the preparation of l -ido-nojirimycin type glyc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::16d62dacc4c75fb4b6925cd4825ec635
https://doi.org/10.1016/j.tet.2010.07.055

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Unambiguous Syntheses of 3-O-Benzyl-1,5-dideoxy-1,5-imino-d-glucitol and -l-iditol

Autor: Péter Fügedi, Zsuzsánna Csíki

Publikováno v: Synthesis. 2010:2626-2630

Short and unambiguous syntheses of 3- O-benzyl-1,5-dideoxy-1,5-imino- D-glucitol and - L-iditolare described. The compound previously reported as 3- O-benzyl-1,5-dideoxy-1,5-imino- D-glucitol (Roy, A.; Achari, B.; Mandal,S. B. SYNTHESIS 2006, 1035)is

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5f9309cce5daaa3cefced0c9e8b46720
https://doi.org/10.1055/s-0029-1218850

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The 4-nitrobenzenesulfonyl group as a convenient N-protecting group for iminosugars—synthesis of oligosaccharide inhibitors of heparanase

Autor: Zsuzsánna Csíki, Péter Fügedi

Publikováno v: Tetrahedron Letters. 51:391-395

The 4-nitrobenzenesulfonyl (nosyl) group can be used advantageously for the protection of the ring nitrogen atom of iminosugars. This group is conveniently introduced, is stable to most of the standard carbohydrate transformations and can be removed

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::74070329d4eb915fd33d0b177996e3a6
https://doi.org/10.1016/j.tetlet.2009.11.042

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