CAS 92236-42-5

3,5-Pyridinedicarboxylic acid, 4-[[[(1S)-1,3-dicarboxypropyl]amino]carbonyl]-1,4-dihydro-2,6-dimethyl-, 3,5-diethyl ester, disodium salt

Description:

3,5-Pyridinedicarboxylic acid, 4-[[[(1S)-1,3-dicarboxypropyl]amino]carbonyl]-1,4-dihydro-2,6-dimethyl-, 3,5-diethyl ester, disodium salt, identified by CAS number 92236-42-5, is a complex organic compound characterized by its pyridine ring structure, which is substituted with multiple functional groups. This compound features two carboxylic acid groups, which contribute to its acidity and potential for forming salts. The presence of diethyl ester groups enhances its solubility in organic solvents and may influence its reactivity. The disodium salt form indicates that the compound can dissociate in solution, making it more soluble in water. Its structure suggests potential applications in pharmaceuticals or as a biochemical reagent, particularly due to the presence of the amino group and the dihydropyridine moiety, which may be involved in various biological interactions. Overall, this compound's unique structural features and functional groups make it a subject of interest in both synthetic and medicinal chemistry.

Formula: C₁₉H₂₆N₂O₉·2Na

InChI: InChI=1S/C19H26N2O9.2Na/c1-5-29-18(27)13-9(3)20-10(4)14(19(28)30-6-2)15(13)16(24)21-11(17(25)26)7-8-12(22)23;;/h11,15,20H,5-8H2,1-4H3,(H,21,24)(H,22,23)(H,25,26);;/t11-;;/m0../s1

InChI key: InChIKey=JRCCJCWLMHKELC-IDMXKUIJSA-N

SMILES: C(N[C@@H](CCC(O)=O)C(O)=O)(=O)C1C(C(OCC)=O)=C(C)NC(C)=C1C(OCC)=O.[Na]

Synonyms:

• 3,5-Pyridinedicarboxylic acid, 4-[[[(1S)-1,3-dicarboxypropyl]amino]carbonyl]-1,4-dihydro-2,6-dimethyl-, 3,5-diethyl ester, disodium salt
• Glutapyrone
• 3,5-Pyridinedicarboxylic acid, 4-[[(1,3-dicarboxypropyl)amino]carbonyl]-1,4-dihydro-2,6-dimethyl-, 3,5-diethyl ester, disodium salt, (S)-

Glutapyrone

CAS: 92236-42-5

Glutapyrone is a polymeric matrix that is composed of glutamic acid, polyethylene glycol, and polyvinyl alcohol. It is used to treat acute liver failure by reducing the amount of free fatty acids in the blood. Glutapyrone prevents the formation of conjugates with fatty acids and also has antioxidative activity. In rat kidneys, glutapyrone reduces the level of ubiquitin-proteasome system and increases mitochondrial membrane potential. This drug also has respiratory control effects, which may be due to its ability to increase mitochondrial membrane potential and reduce respiratory chain inhibition caused by lipopolysaccharide.

Formula: C₁₉H₂₄N₂Na₂O₉

Purity: Min. 95%

Molecular weight: 470.4 g/mol

Ref: 3D-SDA23642