CAS 5779-39-5

3,4,6-Trideoxy-3-(dimethylamino)-D-xylo-hexose

Description:

3,4,6-Trideoxy-3-(dimethylamino)-D-xylo-hexose, with the CAS number 5779-39-5, is a carbohydrate derivative characterized by the presence of a dimethylamino group and the absence of hydroxyl groups at specific positions on the sugar backbone. This compound is a hexose, meaning it contains six carbon atoms, and it is classified as a deoxy sugar due to the removal of hydroxyl groups at the 3, 4, and 6 positions. The presence of the dimethylamino group introduces basic properties, which can influence its reactivity and interactions in biological systems. This compound may exhibit unique solubility characteristics and can participate in various chemical reactions typical of sugars, such as glycosylation. Its structural features suggest potential applications in medicinal chemistry, particularly in the design of glycosylated drugs or as a building block for more complex carbohydrate-based molecules. Overall, 3,4,6-Trideoxy-3-(dimethylamino)-D-xylo-hexose represents an interesting compound for further research in both synthetic and biological chemistry contexts.

Formula: C₈H₁₇NO₃

InChI: InChI=1S/C8H17NO3/c1-6(11)4-7(9(2)3)8(12)5-10/h5-8,11-12H,4H2,1-3H3/t6-,7+,8+/m1/s1

InChI key: InChIKey=VTJCSBJRQLZNHE-CSMHCCOUSA-N

SMILES: [C@@H]([C@H](C=O)O)(C[C@@H](C)O)N(C)C

Synonyms:

• 3,4,6-Trideoxy-3-(dimethylamino)-<span class="text-smallcaps">D</span>-xylo-hexose
• 4-Dimethylaminotetrahydro-6-methylpyran-2,3-diol
• 5779-39-5
• <span class="text-smallcaps">D</span>-Desosamine
• <span class="text-smallcaps">D</span>-xylo-Hexose, 3,4,6-trideoxy-3-(dimethylamino)-
• Desosamine
• Picrocine
• Pikrocin
• 3,4,6-Trideoxy-3-(dimethylamino)-beta-D-xylo-hexopyranose
• D-Desosamine
• 3,4,6-Trideoxy-3-(dimethylamino)-D-xylo-hexose

D-Desosamine

CAS: 5779-39-5

D-Desosamine is a chemical compound that has been isolated from human serum. It is an enzyme inhibitor that inhibits the activity of enzymes such as phosphatases, kinases, and proteases. D-Desosamine also has a matrix effect, which can be used to modify the properties of polymer matrices in order to improve their biocompatibility and mechanical properties. The molecular docking analysis indicated that desosamine can bind to bacterial serine/threonine protein kinase Streptococcus pyogenes phage T4 (SpyPK) and inhibit its activity. This inhibition may be due to the transfer reactions caused by desosamine binding to the enzyme's active site and blocking it. Structural analysis showed that D-desosamine forms hydrogen bonds with amino acids in SpyPK's active site, forming a covalent bond with cysteine residue Cys240. D-Desosamine has been shown to have anti-bacterial properties against

Purity: Min. 95%

Ref: 3D-MD58368

Desosamine

CAS: 5779-39-5

Formula: C₈H₁₇NO₃

Molecular weight: 175.23

Ref: ST-EA-CP-A37023