Iprindole hydrochloride
Iprindole hydrochloride, an opioid receptor agonist, is a tricyclic antidepressant. Iprindole hydrochloride shortens the immobility time in mice forced swimming test, which can be reversed by the opiate antagonist Naloxone (HY-17417A). Iprindole hydrochloride induces lamellar body formation but devoid of lamellar bodies. Iprindole hydrochloride can be used for the research of depression.
Nos produits utilisent uniquement pour la recherche. Nous ne vendons pas aux patients.
- CAS No.: 20432-64-8
- Formule: C19H29ClN2
- Masse moléculaire:320.90
-
Stockage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Voir tous les produits spécifiques à Isoform Opioid Receptor
More
Activité biologique
Description
In Vitro
Iprindole (0.1-10 μM; 8 h) hydrochloride induces the formation of lamellar bodies in L-2 cells[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
In Vivo
Iprindole (10-50 mg/kg; i.p.; single dose) hydrochloride shortens the immobility time in male ICR Swiss mice forced swimming test[2].
Iprindole hydrochloride's (20 mg/kg; i.p.; single dose) activity is reserved by the opiate antagonist Naloxone in male ICR Swiss mice forced swimming test[2].
Iprindole hydrochloride's (10 mg/kg; i.p.; single dose) activity is enhanced by inhibitor of its degradation Bestatin (HY-B0134) or Thiorphan (HY-W013375)) in male ICR Swiss mice forced swimming test[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Animal Model:Domestic cats[1]
-
Dosage:1.0 mg/kg; 2.0 mg/kg; 5.0 mg/kg; 20 mg/kg; 40 mg/kg
-
Administration:i.p.; single dose
-
Result:Did not significantly reduce REM sleep compared to population standards.
Did not significantly affect NREM sleep, wakefulness, or indeterminate periods.
-
Animal Model:ICR Swiss mice (male, 20-25 g, forced swimming test)[2]
-
Dosage:10 mg/kg; 20 mg/kg; 50 mg/kg
-
Administration:i.p.; single dose
-
Result:Shortened the immobility time.
-
Animal Model:ICR Swiss mice (male, 20-25 g, forced swimming test)[2]
-
Dosage:20 mg/kg plus Naloxone (1 mg/kg)
-
Administration:i.p.; single dose
-
Result:Activity was reserved by the opiate antagonist Naloxone.
-
Animal Model:ICR Swiss mice (male, 20-25 g, forced swimming test)[2]
-
Dosage:10 mg/kg plus Bestatin or
Thiorphan(10 μg/kg) -
Administration:i.p.; single dose
-
Result:Further decreased the immobility time.
Chemical Information
-
CAS No. 20432-64-8
-
Masse moléculaire 320.90
-
Formule C19H29ClN2
-
SMILES
CN(C)CCCN1C(CCCCCC2)=C2C3=C1C=CC=C3.Cl
-
Livraison
Room temperature in continental US; may vary elsewhere.
-
Stockage
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureté et documentation
Références
[1]. Baxter BL, et al. Iprindole: an antidepressant which does not block REM sleep. Nature. 1969 Aug 16;223(5207):750-2. [Content Brief]
[2]. de Felipe MC, et al. Antidepressant action of imipramine and iprindole in mice is enhanced by inhibitors of enkephalin-degrading peptidases. Eur J Pharmacol. 1989 Jan 10;159(2):175-80. [Content Brief]
[3]. Martin WJ 2nd, et al. Iprindole reverses the lamellar body deficiency of cultured L-2 cells. Possible implications in the reversal of surfactant deficiency. Am J Pathol. 1987 Oct;129(1):34-43. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)