1. GPCR/G Protein
    Neuronal Signaling
  2. Neurokinin Receptor
  3. Saredutant

Saredutant (Synonyms: SR 48968; SR 48968C)

Cat. No.: HY-106910
Handling Instructions

Saredutant is a selective NK2 receptor antagonist.

For research use only. We do not sell to patients.

Saredutant Chemical Structure

Saredutant Chemical Structure

CAS No. : 142001-63-6

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Saredutant is a selective NK2 receptor antagonist.

IC50 & Target[1]



In Vivo

Saredutant, an NK2 receptor antagonist, has both antidepressant-like effects and synergizes with desipramine in an animal model of depression. Saredutant has dose-dependent effects on swim test immobility, with the low dose of 1 mg/kg having no effect and the doses of 3 and 10 mg/kg significantly reducing immobility[1].

Clinical Trial
Molecular Weight







CC(NC1(C2=CC=CC=C2)CCN(CC[[email protected]@H](C3=CC(Cl)=C(Cl)C=C3)CN(C)C(C4=CC=CC=C4)=O)CC1)=O


Room temperature in continental US; may vary elsewhere


Please store the product under the recommended conditions in the Certificate of Analysis.

Animal Administration

In the first experiment the dose-related effects of Saredutant are investigated. The Flinders Sensitive Line (FSL) rats (n=8) are treated with one of the following: vehicle (carboxymethylcellulose-CMC) or 1, 3, or 10 mg/kg Saredutant, or 5 mg/kg Desipramine as a positive control. Saredutant is injected at 1 mL/kg. The Flinders Resistant Line (FRL) rats are given CMC or 3 mg/kg Saredutant. All injections are i.p. and are given for 14 consecutive days. Approximately 22 h after the last injections the rats are placed in the social interaction chamber with similarly treated rats for a 5-min recording. Then about 2 h later the rats are individually tested in the forced swim test for a single 5-min session[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

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