γ-GT

CAS No. 63699-78-5

γ-GT ( H-GLA(PNA)-OH )

Catalog No. M20155 CAS No. 63699-78-5

γ-GT is used as a synthetic substrate for gamma-glutamyltransferase (GGT) to determine GGT activity.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
50MG 70 In Stock
100MG 97 In Stock
200MG 155 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    γ-GT
  • Note
    Research use only not for human use.
  • Brief Description
    γ-GT is used as a synthetic substrate for gamma-glutamyltransferase (GGT) to determine GGT activity.
  • Description
    γ-GT is used as a synthetic substrate for gamma-glutamyltransferase (GGT) to determine GGT activity.
  • Synonyms
    H-GLA(PNA)-OH
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    γ-glutamyl transferase
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    63699-78-5
  • Formula Weight
    328.28
  • Molecular Formula
    C12H16N4O7
  • Purity
    >98% (HPLC)
  • Solubility
    H2O:30 mg/mL (91.39 mM)
  • SMILES
    N.N[C@@H](CCC(=O)Nc1ccc(c(c1)C(O)=O)[N+]([O-])=O)C(O)=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Shaw LM et al. Gamma-Glutamyltransferase: kinetic properties and assay conditions when gamma-glutamyl-4-nitroanilide and its 3-carboxy derivative are used as donor substrates. Clin Chem. 1977 Jan;23(1):79-85.
molnova catalog
related products
  • Silibinin

    Silibinin, the main flavonoid extracted from the milk thistle Silybum marianum, displays hepatoprotective properties in acute and chronic liver injury.

  • Laurocapram

    Laurocapram is a percutaneous enhancer. Upon application to the skin, laurocapram interacts with lipids in the stratum corneum and may enhance the ability of the skin to absorb a hydrophilic chemical.

  • N-Formyl-Met-Leu-Phe...

    N-Formyl-Met-Leu-Phe-Lys (fMLFK) is a peptide, acts as a potent and selective agonist of FPR1, with EC50s of 3.5 nM, 6.7 μM and 0.88 μM for FPR1, FPR2 and FPR2-D2817.32G, respectively.