GYKI 52466 HYDROCHLORIDE

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GYKI 52466 HYDROCHLORIDE manufacturers

  • GYKI-52466
  • GYKI-52466 pictures
  • $1520.00
  • 2026-05-11
  • CAS:102771-26-6
  • Purity:
  • Supply Ability: 10g
GYKI 52466 HYDROCHLORIDE Basic information
Product Name:GYKI 52466 HYDROCHLORIDE
Synonyms:gyki52466;4-(8-METHYL-9H-1,3-DIOXOLO[4,5-H][2,3]BENZODIAZEPIN-5-YL)-BENZENAMINE HYDROCHLORIDE;GYKI 52466 HYDROCHLORIDE;4-(8-Methyl-(9H)-1,3-dioxolo[4.5-h][2.3]benzodiazepine-5-yl)benzenaminehydrochloride;GYKI52466HCl;1-(4-Aminophenyl)-4-methyl-7,8-(methylenedioxy)-5H-2,3-benzodiazepine;4-(8-Methyl-9H-1,3-dioxolo[4,5-h][2,3]benzodiazepine-5-yl)aniline;1-(p-Aminophenyl)-4-methyl-7,8-methylenedioxy-5H-2,3-benzodiazepine hydrochloride
CAS:102771-26-6
MF:C17H16ClN3O2
MW:329.78
EINECS:
Product Categories:Amines, Aromatics, Heterocycles, Pharmaceuticals, Intermediates & Fine Chemicals
Mol File:102771-26-6.mol
GYKI 52466 HYDROCHLORIDE Structure
GYKI 52466 HYDROCHLORIDE Chemical Properties
Boiling point 472.8±45.0 °C(Predicted)
density 1.39
storage temp. Desiccate at RT
solubility DMSO: 0.39 mg/mL
form solid
pka8.14±0.20(Predicted)
color yellow
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 22-26-36
WGK Germany 3
MSDS Information
ProviderLanguage
SigmaAldrich English
GYKI 52466 HYDROCHLORIDE Usage And Synthesis
Uses4-(8-Methyl-9H-1,3-dioxolo[4,5-h][2,3]benzodiazepin-5-yl)benzenamine is a non-competitive AMPA receptor antagonist and was found to have therapeutic potential for cocaine addiction treatment.
DefinitionChEBI: GYKI 52466 is a benzodiazepine.
Biological ActivitySelective non-competitive AMPA receptor antagonist (IC 50 values are 10-20, ~ 450 and >> 50 μ M for AMPA- , kainate- and NMDA-induced responses respectively). Skeletal muscle relaxant and orally-active anticonvulsant. Has anti-proliferative effects in transformed cells. Also available as part of the AMPA Receptor Tocriset™ . Also available as part of the Kainate Receptor Tocriset™ .
in vivo

GYKI 52466 (intraperitoneal injection; 1.76-13.2 mg/kg; once) treatment provides potent anticonvulsant protection against sound-induced seizures in DBA/2 mice[2].

Animal Model:Male and female DBA/2 mice tested for sound-induced seizure responses[2]
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 ).
IC 50Kainate Receptor: 11 μM (IC50)
storageroom temperature (desiccate)
GYKI 52466 HYDROCHLORIDE Preparation Products And Raw materials
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