
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)






Size | Price / USD | Stock | Quantity |
5MG | 50 | In Stock |
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10MG | 84 | In Stock |
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25MG | 149 | In Stock |
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50MG | 248 | In Stock |
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100MG | 371 | In Stock |
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500MG | 845 | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NameL-701324
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NoteResearch use only, not for human use.
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Brief DescriptionA potent, orally active antagonist at the glycine modulatory site on NMDA receptor with IC50 of 2 nM.
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DescriptionA 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.
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In Vitro——
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In VivoL-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.
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SynonymsL-701,324
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PathwayMembrane Transporter/Ion Channel
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TargetiGluR
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RecptorNMDA receptor
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Research AreaNeurological Disease
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IndicationAnxiety
Chemical Information
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CAS Number142326-59-8
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Formula Weight363.7938
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Molecular FormulaC21H14ClNO3
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Purity>98% (HPLC)
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SolubilityDMSO: ≥ 34 mg/mL
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SMILESO=C1NC2=C(C=CC(Cl)=C2)C(O)=C1C3=CC=CC(OC4=CC=CC=C4)=C3
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Chemical Name2(1H)-Quinolinone, 7-chloro-4-hydroxy-3-(3-phenoxyphenyl)-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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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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