CAS 136132-69-9

ALPHA-DELTA-UA-[1->3]-GALNAC SODIUM SALT

Description:

Alpha-Delta-UA-[1->3]-GalNAc sodium salt, identified by its CAS number 136132-69-9, is a glycosaminoglycan derivative that plays a significant role in biological processes, particularly in cell signaling and molecular recognition. This compound is characterized by its structural components, which include a uronic acid and N-acetylgalactosamine (GalNAc) linked through a specific glycosidic bond. The sodium salt form enhances its solubility in aqueous solutions, making it suitable for various biochemical applications. Its unique structure allows it to interact with proteins and other biomolecules, influencing cellular functions such as proliferation, differentiation, and adhesion. Additionally, this compound may exhibit anticoagulant properties and has potential therapeutic applications in areas such as regenerative medicine and drug delivery systems. Overall, Alpha-Delta-UA-[1->3]-GalNAc sodium salt is a versatile substance with significant implications in biochemistry and pharmacology.

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

Chondroitin disaccharide Deltadi-0S sodium salt

CAS: 136132-69-9

Formula: C₁₄H₂₀NNaO₁₁

Purity: 95%

Molecular weight: 401.2985

Ref: IN-DA009C1I

Chondroitin disaccharide di-0S sodium salt

CAS: 136132-69-9

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: C₁₄H₂₀NNaO₁₁

Purity: Min. 95 Area-%

Color and Shape: Powder

Molecular weight: 402.31 g/mol

Ref: 3D-OC28897