Abstract
The title compound, C12H24NO10
+·Cl−·H2O, (I), crystallizes in the monoclinic space group P21 and exists as a monohydrate of a monosubstituted ammonium chloride salt, with the reducing carbohydrate portion existing exclusively as the α-pyranose tautomer. The glycosidic bond geometry in (I) is stabilized by an intramolecular hydrogen bond and is close to that found in crystalline α-lactose. All heteroatoms except glucopyranose ring O4 participate in an extensive hydrogen-bonding network, which propagates in all directions in the crystal structure of (I).
Funder
University of Missouri, Agriculture Experiment Station Chemical Laboratories
National Institute of Food and Agriculture
Publisher
International Union of Crystallography (IUCr)
Subject
Rehabilitation,Physical Therapy, Sports Therapy and Rehabilitation,General Medicine
Reference22 articles.
1. Demonstration of poly-N-acetyl lactosamine residues in ameboid and ramified microglial cells in rat brain by tomato lectin binding.
2. Soluble ?-galactosyl-binding lectin (galectin) from toad ovary: Crystallographic studies of two protein-sugar complexes
3. Glycosylation, galectins and cellular signaling
4. Bruker (2016). APEX, SAINT and AXScale. Bruker AXS Inc., Madison, Wisconsin, USA.
5. Dekany, G., Ágoston, K., Bajza, I., Bøjstrup, M., Pérez, I. F., Kröger, L. & Röhrig, C. H. (2014). US Patent 8,796,434.