D5764

2,3-Diphospho-D-glyceric acid pentasodium salt

glycolysis metabolite

• Sinónimos: 2,3-DPG, D-Glycerate 2,3-diphosphate sodium salt
• Fórmula lineal: C₃H₃O₁₀P₂Na₅
• Número CAS: 102783-53-9
• Peso molecular: 375.95
• NACRES: NA.25
• PubChem Substance ID: 24893967
• UNSPSC Code: 12352201
• MDL number: MFCD00070074

Propiedades

• biological source: synthetic
• Quality Level: 200
• form: powder
• impurities: 3-phosphoglyceric acid, essentially free
• color: white to off-white
• solubility: water: 100 mg/mL, clear, colorless to faintly yellow
• cation traces: Na: 24.5-32.5% (anhydrous)
• storage temp.: −20°C
• SMILES string: [Na].OC(=O)[C@@H](COP(O)(O)=O)OP(O)(O)=O
• InChI: 1S/C3H8O10P2.Na.H/c4-3(5)2(13-15(9,10)11)1-12-14(6,7)8;;/h2H,1H2,(H,4,5)(H2,6,7,8)(H2,9,10,11);;/t2-;;/m1../s1
• InChI key: JJEMSNINYKJOBZ-YBBRRFGFSA-N

Descripción

Application

D-Glycerate 2,3-diphosphate, cofactor of both phosphoglyceric acid mutase and hemoglobin, may be used as a reference compound in analysis of blood cell (erythrocyte) glycolysic cycle metabolites.

Biochem/physiol Actions

Metabolite of glycolysis within human erythrocytes produced by 2,3-diphosphoglycerate mutase in an alternative to the glycolytic pathway. Binds to hemaglobin to reduce oxygenation.

Other Notes

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Información de seguridad

• Clase de almacenamiento: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)