Fenobam

CAS No. 57653-26-6

Fenobam( —— )

Catalog No. M26686 CAS No. 57653-26-6

Fenobam shows inverse agonist activity which blocks the mGlu5 receptor basal activity(IC50: 84 nM). Fenobam has anxiolytic activity.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 84 In Stock
5MG 55 In Stock
10MG 98 In Stock
25MG 164 In Stock
50MG 242 In Stock
100MG 351 In Stock
200MG 486 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Fenobam
  • Note
    Research use only, not for human use.
  • Brief Description
    Fenobam shows inverse agonist activity which blocks the mGlu5 receptor basal activity(IC50: 84 nM). Fenobam has anxiolytic activity.
  • Description
    Fenobam shows inverse agonist activity which blocks the mGlu5 receptor basal activity(IC50: 84 nM). Fenobam has anxiolytic activity. Fenobam is a selective and non-competitive mGluR5 antagonist acting at an allosteric modulatory site (Kd values are 54 and 31 nM for rat and human recombinant mGlu5 receptors, respectively).(In Vivo):Fenobam sulfate (30-60 mg/kg; p.o.) inhibited cocaine self-administration significantly .
  • In Vitro
    ——
  • In Vivo
    Animal Model:Male Long-Evans rats (250-300 g)Dosage:30-60 mg/kg Administration:P.o.Result:Inhibited self-administration
  • Synonyms
    ——
  • Pathway
    Neuroscience
  • Target
    GluR
  • Recptor
    MAGL
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    57653-26-6
  • Formula Weight
    266.69
  • Molecular Formula
    C11H11ClN4O2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (374.98 mM)
  • SMILES
    CN1CC(=O)N=C1NC(=O)Nc1cccc(Cl)c1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Shuhei Ikeda, et al. Design and Synthesis of Novel Spiro Derivatives as Potent and Reversible Monoacylglycerol Lipase (MAGL) Inhibitors: Bioisosteric Transformation from 3-Oxo-3,4-dihydro-2 H-benzo[ b][1,4]oxazin-6-yl Moiety. J Med Chem. 2021 Aug 12;64(15):11014-11044.
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