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M2433935

Etifoxine , ≥99% , 21715-46-8

CAS NO.:21715-46-8

Empirical Formula: C17H17ClN2O

Molecular Weight: 300.78

MDL number: MFCD00868190

Pack Size Price Stock Quantity
5mg RMB711.20 In Stock
10mg RMB734.40 In Stock
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Update time: 2022-07-08

PRODUCT Properties

Melting point: 90-92℃
Boiling point: 421.2±55.0 °C(Predicted)
Density  1.1716 (rough estimate)
vapor pressure  0-1Pa at 20-25℃
refractive index  1.5800 (estimate)
storage temp.  Store at -20°C
solubility  DMSO:60.0(Max Conc. mg/mL);199.47(Max Conc. mM)
DMF:30.0(Max Conc. mg/mL);99.74(Max Conc. mM)
DMF:PBS (pH 7.2) (1:8):0.1(Max Conc. mg/mL);0.33(Max Conc. mM)
Ethanol:20.0(Max Conc. mg/mL);66.49(Max Conc. mM)
pka 4.89±0.40(Predicted)
form  Solid:particulate/powder
color  Light yellow to yellow
LogP 4.09-4.52 at 21-25℃ and pH7

Description and Uses

Etifoxine is a positive allosteric modulator of α1β2γ2 and α1β3γ2 subunit-containing GABAA receptors.1 It selectively increases GABA-induced currents in X. laevis oocytes expressing α1β2γ2 or α1β3γ2 over α1β1γ2 subunit-containing receptors at 20 µM. Etifoxine inhibits binding of the GABAA receptor agonist muscimol in rat corticol membranes with a Kd value of 23 nM in a radioligand binding assay.2 It increases NGF-induced neurite outgrowth in PC12 cells when used at a concentration of 20 µM.3 Etifoxine (12.5 mg/kg, i.p.) increases the percentage of time spent in the open arms of the elevated plus maze in high-anxiety BALB/cByJ, but not C57BL/6, mice, indicating anxiolytic-like activity.4 It increases the seizure threshold in a mouse model of seizures induced by picrotoxin (Item No. 20771) with a minimum effective dose (MED) of 75 mg/kg.2 Etifoxine (50 mg/kg, i.p.) also increases the paw withdrawal threshold on the ipsilateral side in a rat model of rheumatoid arthritis induced by complete Freund's adjuvant.5WARNING This product is not for human or veterinary use.

Safety

Symbol(GHS)  Exclamation Mark (GHS07)Environment (GHS09)
GHS07,GHS09
Signal word  Warning
Hazard statements  H401-H302
Precautionary statements  P264-P270-P301+P312-P330-P501-P273-P501
Toxicity LD50 orally in mice: 12 g/kg (Hoffmann)
REACH Registrations Active

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