NADP disodium salt

CAS No. 24292-60-2

NADP disodium salt( Disodium NADP | Triphosphopyridine nucleotide disodium salt )

Catalog No. M27584 CAS No. 24292-60-2

NADP disodium salt is a nicotinamide adenine dinucleotide. NADP disodium salt is a key redox cofactor for electron transfer in the metabolism, serves as an electron carrier in a number of reactions, being alternately oxidized (NADP+) and reduced (NADPH).

NADP disodium salt is a nicotinamide adenine dinucleotide. NADP disodium salt is a key redox cofactor for electron transfer in the metabolism, serves as an electron carrier in a number of reactions, being alternately oxidized (NADP+) and reduced (NADPH).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
100MG 49 In Stock
200MG 79 In Stock
500MG 147 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    NADP disodium salt
  • Note
    Research use only, not for human use.
  • Brief Description
    NADP disodium salt is a nicotinamide adenine dinucleotide. NADP disodium salt is a key redox cofactor for electron transfer in the metabolism, serves as an electron carrier in a number of reactions, being alternately oxidized (NADP+) and reduced (NADPH).
  • Description
    NADP disodium salt is a nicotinamide adenine dinucleotide. NADP disodium salt is a key redox cofactor for electron transfer in the metabolism, serves as an electron carrier in a number of reactions, being alternately oxidized (NADP+) and reduced (NADPH).
  • In Vitro
  • In Vivo
  • Synonyms
    Disodium NADP | Triphosphopyridine nucleotide disodium salt
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    mGlu7
  • Research Area
  • Indication

Chemical Information

  • CAS Number
    24292-60-2
  • Formula Weight
    787.372
  • Molecular Formula
    C21H26N7Na2O17P3
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?H2O : 250 mg/mL (316.70 mM)
  • SMILES
    [Na+].[Na+].NC(=O)c1ccc[n+](c1)[C@@H]1O[C@H](COP([O-])(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](OP([O-])([O-])=O)[C@@H]2O)n2cnc3c(N)ncnc23)[C@@H](O)[C@H]1O
  • Chemical Name

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Gentaroh Suzuki, et al. In vitro pharmacological characterization of novel isoxazolopyridone derivatives as allosteric metabotropic glutamate receptor 7 antagonists. J Pharmacol Exp Ther. 2007 Oct;323(1):147-56.
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