18311-26-7Relevant articles and documents
Sugar derivatives as new 6-phosphogluconate dehydrogenase inhibitors selective for the parasite Trypanosoma brucei
Pasti, Claudia,Rinaldi, Eliana,Cervellati, Carlo,Dallocchio, Franco,Hardre, Renaud,Salmon, Laurent,Hanau, Stefania
, p. 1207 - 1214 (2003)
Sugar derivatives mimicking compounds which take part in the catalysed reaction have been assayed as alternative substrates and/or competitive inhibitors of 6-phosphogluconate dehydrogenase from Trypanosoma brucei and sheep liver. Phosphonate analogues ha
Ring-opening polymerization of lactones using binaphthyl-diyl hydrogen phosphate as organocatalyst and resulting monosaccharide functionalization of polylactones
Miao, Yong,Phuphuak, Yupin,Rousseau, Cyril,Bousquet, Till,Mortreux, Andre,Chirachanchai, Suwabun,Zinck, Philippe
, p. 2279 - 2287 (2013)
Binaphthyl-diyl hydrogen phosphate has been assessed for the first time as a catalyst for the ring-opening polymerization of ε-caprolactone (CL) and δ-valerolactone (VL). In the presence of benzyl alcohol as coinitiator at 40-60 °C, the polymerization is
Peptide-Coated Platinum Nanoparticles with Selective Toxicity against Liver Cancer Cells
Shoshan, Michal S.,Vonderach, Thomas,Hattendorf, Bodo,Wennemers, Helma
, p. 4901 - 4905 (2019)
Peptide-stabilized platinum nanoparticles (PtNPs) were developed that have significantly greater toxicity against hepatic cancer cells (HepG2) than against other cancer cells and non-cancerous liver cells. The peptide H-Lys-Pro-Gly-dLys-NH2 was identified by a combinatorial screening and further optimized to enable the formation of water-soluble, monodisperse PtNPs with average diameters of 2.5 nm that are stable for years. In comparison to cisplatin, the peptide-coated PtNPs are not only more toxic against hepatic cancer cells but have a significantly higher tumor cell selectivity. Cell viability and uptake studies revealed that high cellular uptake and an oxidative environment are key for the selective cytotoxicity of the peptide-coated PtNPs.
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Luckett,Smith
, p. 1506,1510 (1940)
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Chemoenzymatic synthesis of 3-deoxy-3-fluoro-l-fucose and its enzymatic incorporation into glycoconjugates
Valverde, Pablo,Vendeville, Jean-Baptiste,Hollingsworth, Kristian,Mattey, Ashley P.,Keenan, Tessa,Chidwick, Harriet,Ledru, Helene,Huonnic, Kler,Huang, Kun,Light, Mark E.,Turner, Nicholas,Jiménez-Barbero, Jesús,Galan, M. Carmen,Fascione, Martin A.,Flitsch, Sabine,Turnbull, W. Bruce,Linclau, Bruno
supporting information, p. 6408 - 6411 (2020/06/21)
The first synthesis of 3-deoxy-3-fluoro-l-fucose is presented, which employs ad- tol-sugar translation strategy, and involves an enzymatic oxidation of 3-deoxy-3-fluoro-l-fucitol. Enzymatic activation (FKP) and glycosylation using an α-1,2 and an α-1,3 fu
Chemical synthesis and preliminary biological evaluation of C-6-O-methyl-1-deoxynojirimycin as a potent α-glucosidase inhibitor
Wang, Lin,Liang, Tingting,Fang, Zhijie
, p. 36 - 49 (2019/12/24)
A facile and efficient synthesis of 6-O-methyl-1-deoxynojirimycin 4 from commercially available methyl α-D-glucopyranoside in 10 steps and 25% overall yield was reported. The synthetic strategy was based on the regioselective protection/deprotection at 6-