121363-59-5Relevant articles and documents
Solid-state 17O NMR analysis of synthetically 17O-enriched D-glucosamine
Yamada, Kazuhiko,Yamaguchi, Yoshiki,Uekusa, Yoshinori,Aoki, Kazumasa,Shimada, Ichio,Yamaguchi, Takumi,Kato, Koichi
, (2020/04/17)
The hydroxyl groups of carbohydrates are critical determinants of their conformational dynamics and intermolecular interactions but are difficult to characterize by conventional 1H nuclear magnetic resonance (NMR) approaches in solution. Here,
Mechanism of multivalent carbohydrate-protein interactions studied by EPR spectroscopy
Braun, Patrick,N?gele, Bettina,Wittmann, Valentin,Drescher, Malte
supporting information; scheme or table, p. 8428 - 8431 (2011/10/31)
From a distance: Distance measurements in the nanometer range by means of spin-label electron paramagnetic resonance provide structural evidence for multivalent protein-ligand interactions in solution (see picture; protein subunits: blue/green, ligand: bl
Synthesis of hyperbranched aminopolysaccharides
Kadokawa, Jun-Ichi,Sato, Mitsuru,Karasu, Masa,Tagaya, Hideyuki,Chiba, Koji
, p. 2373 - 2376 (2007/10/03)
Sugar dihydroozaxole monomers with two free hydroxyl groups undergo acid-catalyzed polymerization to hyperbranched aminopolysaccharides [Eq. (a)]. Their molecular weights were determined by the light-scattering method to be between 2.3 x 105 an