Oxiracetam

CAS No. 62613-82-5

Oxiracetam( Oxiracetam | ISF-2522 | Neuractiv | Hydroxypiracetam )

Catalog No. M15370 CAS No. 62613-82-5

Oxiracetam, a cyclic derivative of gamma-aminobutyric acid (GABA), is used as a nootropic drug to improve memory and learning.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 62 In Stock
5MG 48 In Stock
10MG 72 In Stock
25MG 112 In Stock
50MG 138 In Stock
100MG 216 In Stock
200MG 325 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Oxiracetam
  • Note
    Research use only, not for human use.
  • Brief Description
    Oxiracetam, a cyclic derivative of gamma-aminobutyric acid (GABA), is used as a nootropic drug to improve memory and learning.
  • Description
    Oxiracetam, a cyclic derivative of gamma-aminobutyric acid (GABA), is used as a nootropic drug to improve memory and learning.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Oxiracetam | ISF-2522 | Neuractiv | Hydroxypiracetam
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    GAT
  • Recptor
    GABAR
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    62613-82-5
  • Formula Weight
    158.16
  • Molecular Formula
    C6H10N2O3
  • Purity
    >98% (HPLC)
  • Solubility
    Water: 31 mg/mL (196.0 mM); DMSO: 31 mg/mL (196.0 mM)
  • SMILES
    O=C(N)CN1C(CC(O)C1)=O
  • Chemical Name
    4-Hydroxy-2-oxopyrrolidine-N-acetamide

Shipping & Storage Information

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

Reference

1.Sansone M, et al. Arch Int Pharmacodyn Ther. 1985, 275(1), 86-92.
molnova catalog
related products
  • CI-966

    CI-966 (PD 126141) is a potent, selective inhibitor of the GABA transporter GAT-1 with IC50 of 0.26 and 1.2 uM for human and rat GAT-1, respectively.

  • NNC 05-2090 hydrochl...

    NNC 05-2090 is a potent selective GABA transporter inhibitor of mGAT2 with Ki of 1.4 uM.

  • Pagoclone

    A potent, orally active GABAA receptor agonist with high affinity (0.7-9.1nM) to the benzodiazepine binding site of GABAA receptors containing either an α1, α2, α3 or α5 subunit.