Eliprodil

CAS No. 119431-25-3

Eliprodil( SL-820715 )

Catalog No. M10679 CAS No. 119431-25-3

Eliprodil (SL-820715) is a non-competitive NR2B-NMDA receptor antagonist, less potent for NR2A- and NR2C-containing receptors (IC50>100 uM).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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10MG 83 In Stock
25MG 159 In Stock
50MG 304 In Stock
100MG 462 In Stock
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Biological Information

  • Product Name
    Eliprodil
  • Note
    Research use only, not for human use.
  • Brief Description
    Eliprodil (SL-820715) is a non-competitive NR2B-NMDA receptor antagonist, less potent for NR2A- and NR2C-containing receptors (IC50>100 uM).
  • Description
    Eliprodil (SL-820715) is a non-competitive NR2B-NMDA receptor antagonist, less potent for NR2A- and NR2C-containing receptors (IC50>100 uM); inhibits [3H]norepinephrine release from cortical and hippocampal slices but enhances the basal efflux of endogenous and tritiated dopamine from striatal slices, also blocks the uptake of [3H]dopamine into striatal synaptosomes with IC50 of 1.5 uM; reduces the volume of infarction in models of focal cerebral ischemia.Stroke Phase 3 Discontinued.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    SL-820715
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    iGluR
  • Recptor
    NR2B-NMDA
  • Research Area
    Neurological Disease
  • Indication
    Stroke

Chemical Information

  • CAS Number
    119431-25-3
  • Formula Weight
    347.8541
  • Molecular Formula
    C20H23ClFNO
  • Purity
    >98% (HPLC)
  • Solubility
    10 mM in DMSO
  • SMILES
    OC(C1=CC=C(Cl)C=C1)CN2CCC(CC3=CC=C(F)C=C3)CC2
  • Chemical Name
    1-Piperidineethanol, α-(4-chlorophenyl)-4-[(4-fluorophenyl)methyl]-

Shipping & Storage Information

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

Reference

1. Woodward JJ, et al. Eur J Pharmacol. 1992 Jan 21;210(3):265-70. 2. Carter CJ, et al. J Pharmacol Exp Ther. 1990 May;253(2):475-82. 3. Carter C, et al. Eur J Pharmacol. 1989 May 30;164(3):611-2. 4. Bath CP, et al. Eur J Pharmacol. 1996 Mar 28;299(1-3):103-12.
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