L-701324

CAS No. 142326-59-8

L-701324( L-701,324 )

Catalog No. M11785 CAS No. 142326-59-8

A potent, orally active antagonist at the glycine modulatory site on NMDA receptor with IC50 of 2 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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5MG 50 In Stock
10MG 84 In Stock
25MG 149 In Stock
50MG 248 In Stock
100MG 371 In Stock
500MG 845 In Stock
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Biological Information

  • Product Name
    L-701324
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent, orally active antagonist at the glycine modulatory site on NMDA receptor with IC50 of 2 nM.
  • Description
    A potent, orally active antagonist at the glycine modulatory site on NMDA receptor with IC50 of 2 nM; is a potent, p.o. active anticonvulsant with a reduced propensity to activate mesolimbic dopaminergic systems in rodents.Anxiety Discontinued.
  • In Vitro
    ——
  • In Vivo
    L-701324 (5-10 mg/kg; i.p.; once) exhibits antidepressant-like potential in the forced swim test (FST) and tail suspension test (TST) without affecting the locomotor activity of mice.L-701324 (5-10 mg/kg; i.p.; daily, for 2 weeks) produces strong antidepressant-like effects in the chronic unpredictable mild stress (CUMS) model of depression and prevents the CUMS-induced decreases in eurogenesis and the BDNF signaling cascade in the hippocampus. L-701324 (2.5-5 mg/kg; p.o.; once) inhibits NMDA receptor activity via a blockade of the NMDA/glycine-sensitive site at the NMDA receptor is accompanied by a reduction of anxiety-like behavior in both non-conditioned and conditioned conflict behavior situations. Animal Model:Male C57BL/6 J mice in the chronic unpredictable mild stress (CUMS) (7 weeks of age) Dosage:5 and 10 mg/kg Administration:Intraperitoneal injection; daily, for 2 weeks Result:Reduced the immobility of C57BL/6 J mice.Increased the expression of BDNF, pTrkB and pCREB in the hippocampus.Animal Model:Male C57BL/6 J mice in the forced swim test (FST) and tail suspension test (TST) (7 weeks of age)Dosage:5 and 10 mg/kg Administration:Intraperitoneal injection; once Result:Reduced the immobility of C57BL/6 J mice in the FST and TST.Animal Model:Male Sprague-Dawley rats (280-300 g)Dosage:2.5 and 5 mg/kg Administration:Oral administration; once Result:Increased in the percentage of time spent in the open arm in a dose-dependent.Increased punished responding in the Vogel's conflict test in a dose-dependent fashion.
  • Synonyms
    L-701,324
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    iGluR
  • Recptor
    NMDA receptor
  • Research Area
    Neurological Disease
  • Indication
    Anxiety

Chemical Information

  • CAS Number
    142326-59-8
  • Formula Weight
    363.7938
  • Molecular Formula
    C21H14ClNO3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: ≥ 34 mg/mL
  • SMILES
    O=C1NC2=C(C=CC(Cl)=C2)C(O)=C1C3=CC=CC(OC4=CC=CC=C4)=C3
  • Chemical Name
    2(1H)-Quinolinone, 7-chloro-4-hydroxy-3-(3-phenoxyphenyl)-

Shipping & Storage Information

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

Reference

1. Kulagowski JJ, et al. J Med Chem. 1994 May 13;37(10):1402-5. 2. Bristow LJ, et al. J Pharmacol Exp Ther. 1996 Nov;279(2):492-501. 3. Hutson PH, et al. Eur J Pharmacol. 1997 May 20;326(2-3):127-32.
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