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L-701324

CAT: 0804-HY-18698-01Size: 5 mgDry Ice: NoHazardous: No
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CAT#:0804-HY-18698-01Size:5 mg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
L-701324 is a potent, orally active NMDA receptor antagonist that antagonizes the activity of the NMDA receptor by blocking its glycine B binding site. L-701324 binds with high affinity to rat brain membranes (IC50=2 nM) . L-701324 has antidepressant activity[1][2][3].
CAS Number
142326-59-8
UNSPSC
12352005
Hazard Statement
H302, H315, H319, H335
Target
IGluR
Type
Reference compound
Related Pathways
Membrane Transporter/Ion Channel; Neuronal Signaling
Applications
Neuroscience-Neurodegeneration
Field of Research
Neurological Disease
Assay Protocol
https://www.medchemexpress.com/L-701324.html
Purity
99.85
Solubility
DMSO : ≥ 34 mg/mL
Smiles
O=C1NC2=C(C=CC(Cl)=C2)C(O)=C1C3=CC=CC(OC4=CC=CC=C4)=C3
Molecular Formula
C21H14ClNO3
Molecular Weight
363.79
Precautions
H302, H315, H319, H335
References & Citations
[1]Liu L, et, al. Antidepressant-like activity of L-701324 in mice: A behavioral and neurobiological characterization. Behav Brain Res. 2021 Feb 5;399:113038.|[2]Kotlinska J, et, al. A characterization of anxiolytic-like actions induced by the novel NMDA/glycine site antagonist, L-701,324. Psychopharmacology (Berl) . 1998 Jan;135 (2) :175-81.|[3]Hutson PH, et, al. L-701,324, a glycine/NMDA receptor antagonist, blocks the increase of cortical dopamine metabolism by stress and DMCM. Eur J Pharmacol. 1997 May 20;326 (2-3) :127-32.
Shipping Conditions
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Scientific Category
Reference compound1
Clinical Information
No Development Reported
Isoform
NMDA Receptor

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Alternative Products

CatalogName
T1909-01L-701324
A15522-50L-701324 50mg
A15522-10L-701324 10mg
A15522-200L-701324 200mg
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A15522-25L-701324 25mg
A15522-5L-701324 5mg
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