![ALPHA-DELTA-UA-[1->3]-GALNAC SODIUM SALT](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F314832-alpha-delta-ua-1-3-galnac-sodium-salt.webp&w=3840&q=75)
CAS 136132-69-9: ALPHA-DELTA-UA-[1->3]-GALNAC SODIUM SALT
Formula:C14H21NNaO11
InChI:InChI=1/C14H21NO11.Na/c1-5(18)15-6(3-16)12(10(21)8(20)4-17)26-14-11(22)7(19)2-9(25-14)13(23)24;/h2-3,6-8,10-12,14,17,19-22H,4H2,1H3,(H,15,18)(H,23,24);
SMILES:CC(=NC(C=O)C(C(C(CO)O)O)OC1C(C(C=C(C(=O)O)O1)O)O)O.[Na]
Synonyms:- Delta-Ua->Galnac Na
- Disaccharide Delta Di-Os
- Chondroitin Disaccharide Delta-Di-Os Sodium Salt
- Chondroitin Unsaturated Disaccharide Deltadi-Os, Sodium Salt
- 2-Acetamido-2-Deoxy-3-O-(Beta-D-Gluco-4-Enepyranosyluronic Acid)-D-Glucose, Na
- Chondroitin Disaccharide Ddi-0S Sodium
- Chondroitin Disaccharide △Di-0S Sodium Salt
- hexose, 2-(acetylamino)-2-deoxy-3-O-(4-deoxyhex-4-enopyranuronosyl)-, monosodium salt
Sort by
Found 2 products.
Chondroitin disaccharide di-0S sodium salt
CAS:The structural analysis of chondroitin disaccharide di-0S sodium salt has been done by a bacterial enzyme, which is an enzyme that catalyzes the hydrolysis of glycosidic bonds. The reaction mechanism is spontaneous and the biochemical analysis indicates that the molecule is a glycosidic bond with hemiketal and hydration. The active site residues are found to be water molecule, which help in binding with the substrate to form a hemiketal. Biochemical analysis of this molecule reveals that it is an oligosaccharide with two sugar molecules linked by glycosidic bond.Formula:C14H20NNaO11Purity:Min. 95 Area-%Color and Shape:PowderMolecular weight:401.3 g/molChondroitin disaccharide di-0S sodium salt
CAS:Formula:C14H21NNaO11Purity:95%Molecular weight:402.3064
