
GYKI 52466 dihydrochloride
CAS No. 102771-26-6
GYKI 52466 dihydrochloride( GYKI52466 dihydrochloride )
Catalog No. M10135 CAS No. 102771-26-6
GYKI 52466 is a selective, non-competitive, orally active AMPA receptor (AMPAR) antagonist with IC50 of 10-20 uM against AMPA-induced responses.
Purity : >98% (HPLC)






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50MG | 1782 | Get Quote |
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100MG | 2250 | Get Quote |
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Biological Information
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Product NameGYKI 52466 dihydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionGYKI 52466 is a selective, non-competitive, orally active AMPA receptor (AMPAR) antagonist with IC50 of 10-20 uM against AMPA-induced responses.
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DescriptionGYKI 52466 is a selective, non-competitive, orally active AMPA receptor (AMPAR) antagonist with IC50 of 10-20 uM against AMPA-induced responses; displays >20-fold selectivity over kainate and NMDA receptors; shows anticonvulsant and neuroprotective properties.Alzheimer Disease Discontinued.
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In VitroGYKI 52466 (0.3-100 μM) inhibits inward currents activated by AMPA and Kainate receptor in cultured rat hippocampal neurons.
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In VivoGYKI 52466 (intraperitoneal injection; 1.76-13.2 mg/kg; once) treatment provides potent anticonvulsant protection against sound-induced seizures in DBA/2 mice. Animal Model:Male and female DBA/2 mice tested for sound-induced seizure responses Dosage:1.76-13.2 mg/kg Administration:Intraperitoneal injection; 1.76-13.2 mg/kg; once Result:Observed Maximal anticonvulsant protection after the i.p. treatment (5-15 min ).
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SynonymsGYKI52466 dihydrochloride
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PathwayMembrane Transporter/Ion Channel
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TargetiGluR
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RecptoriGluR
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Research AreaNeurological Disease
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IndicationAlzheimer Disease
Chemical Information
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CAS Number102771-26-6
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Formula Weight366.24
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Molecular FormulaC17H15N3O2.2HCl
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Purity>98% (HPLC)
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Solubility——
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SMILESNC1=CC=C(C2=NN=C(C)CC3=CC4=C(OCO4)C=C32)C=C1
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Chemical Name4-(8-Methyl-9H-1,3-dioxolo[4,5-h][2,3]benzodiazepin-5-yl)-benzenamine dihydrochloride
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. Tarnawa I, et al. Eur J Pharmacol. 1989 Aug 22;167(2):193-9.
2. Ouardouz M, et al. Neurosci Lett. 1991 Apr 15;125(1):5-8.
3. Donevan SD, et al. Neuron. 1993 Jan;10(1):51-9.
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