PEAQX

CAS No. 459836-30-7

PEAQX( NVP-AAM077 | NVP-AAM 077 | NVP-AAM-077 )

Catalog No. M17513 CAS No. 459836-30-7

PEAQX(NVP-AAM 077) is an effective and orally available NMDA antagonist. It can inhibit human NMDA receptors for 1A/2A(IC50: 270 nM), rather than 1A/2B(29, 600 nM).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 58 In Stock
5MG 105 In Stock
10MG 190 In Stock
25MG 342 In Stock
50MG 532 In Stock
100MG 759 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    PEAQX
  • Note
    Research use only, not for human use.
  • Brief Description
    PEAQX(NVP-AAM 077) is an effective and orally available NMDA antagonist. It can inhibit human NMDA receptors for 1A/2A(IC50: 270 nM), rather than 1A/2B(29, 600 nM).
  • Description
    PEAQX, also known as NVP-AAM077; is a competitive antagonist at the NMDA receptor. Although originally described as 100-fold selective for GluN1/GluN2A receptors vs. GluN1/GluN2B receptors, more detailed studies of the Ki of PEAQX revealed it only shows a 5 fold difference in affinity for GluN1/GluN2A vs. GluN1/GluN2B receptors. It is also a potent anticonvulsant in animal tests.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    NVP-AAM077 | NVP-AAM 077 | NVP-AAM-077
  • Pathway
    Neuroscience
  • Target
    Gamma-secretase
  • Recptor
    hNMDA 1A/2A receptors
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    459836-30-7
  • Formula Weight
    516.2
  • Molecular Formula
    C17H17BrN3Na2O6P
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    O=c1c(=O)[nH]c2c(c(C(P(=O)(O)O)N[C@H](c3ccc(Br)cc3)C)ccc2)[nH]1
  • Chemical Name
    sodium ((((S)-1-(4-bromophenyl)ethyl)amino)(2,3-dioxidoquinoxalin-5-yl)methyl)phosphonate hydrate .

Shipping & Storage Information

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

Reference

1.Auberson YP, et al. Bioorg Med Chem Lett. 2002 Apr 8;12(7):1099-102.
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