GYKI-47261
GYKI-47261 is a competitive, orally active, and selective AMPA receptor antagonist with an IC50 of 2.5 μM. GYKI-47261 has broad spectrum anticonvulsive activity and neuroprotective effects. GYKI-47261 is also a potent inducer of CYP2E1.
For research use only. We do not sell to patients.
- CAS No.: 220445-20-5
- Formula: C18H15ClN4
- Molecular Weight:322.79
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
All iGluR Isoforms
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Biological Activity
Description
In Vivo
GYKI-47261(20 mg/kg; i.p.) reverses the dopamine depleting effect of MPTP[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Male C57 black mice, weighing 23-30 g[1]
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Dosage:20 mg/kg
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Administration:I.p.
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Result:Reversed the MPTP-induced decrease in striatal concentrations.
Chemical Information
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CAS No. 220445-20-5
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Molecular Weight 322.79
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Formula C18H15ClN4
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SMILES
NC1=CC=C(C2=NN3C(CC4=CC=C(Cl)C=C42)=NC(C)=C3)C=C1
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Protocols
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Cell Cytotoxicity Assay
Cytotoxicity assays are usually based on the assessment of cell membrane damage, which can also be indirectly detected by measuring cell viability. Detection methods include MTT assay, CKK-8 assay, LDH assay and ATP assay, etc.
Purity & Documentation
References
[1]. Abrahám G, et al. New non competitive AMPA antagonists. Bioorg Med Chem. 2000;8(8):2127-2143. [Content Brief]
[2]. Tamási V, et al. GYKI-47261, a new AMPA [2-amino-3-(3-hydroxymethylisoxazole-4-yl)propionic acid] antagonist, is a CYP2E1 inducer. Drug Metab Dispos. 2003;31(11):1310-1314. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)