Nefiracetam

CAS No. 77191-36-7

Nefiracetam( —— )

Catalog No. M15918 CAS No. 77191-36-7

Nefiracetam is a GABAergic, cholinergic, and monoaminergic neuronal system enhancer for Ro 5-4864-induced convulsions. Phase 2.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 28 In Stock
100MG 33 In Stock
200MG 44 In Stock
500MG 71 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Nefiracetam
  • Note
    Research use only, not for human use.
  • Brief Description
    Nefiracetam is a GABAergic, cholinergic, and monoaminergic neuronal system enhancer for Ro 5-4864-induced convulsions. Phase 2.
  • Description
    Nefiracetam is a GABAergic, cholinergic, and monoaminergic neuronal system enhancer for Ro 5-4864-induced convulsions. Phase 2.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    GAT
  • Recptor
    GABAR
  • Research Area
    Neurological Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    77191-36-7
  • Formula Weight
    246.31
  • Molecular Formula
    C14H18N2O2
  • Purity
    >98% (HPLC)
  • Solubility
    Ethanol: 49 mg/mL (198.94 mM); Water: 5 mg/mL (20.3 mM); DMSO: 49 mg/mL (198.94 mM)
  • SMILES
    CC1=CC=CC(C)=C1NC(=O)CN1CCCC1=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Shiotani T, et al. Brain Res, 2000, 859(2), 255-26
molnova catalog
related products
  • TPA023

    TPA023 is a potent, α2/α3 subtype-selective, and oral GABAA receptor agonist with Kd of 0.92, 1.05 and 0.58 nM for α1-, α2-, α3-, and α5-containing human receptors.

  • Vigabatrin Hydrochlo...

    Vigabatrin Hcl(γ-Vinyl-GABA; Sabril) is a structural analog of the inhibitory neurotransmitter γ-aminobutyric acid (GABA) that irreversibly inhibits the catabolism of GABA by GABA transaminase.

  • Flumazenil

    Flumazenil(Ro 15-1788) is a benzodiazepine antagonist, non-selective for α1, α2, α3 or α5-containing GABAA receptors.