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

Ezlopitant (CJ-11,974) is a selective, non-peptidic neurokinin-1 (NK-1)-receptor antagonist. Ezlopitant inhibits both acute and delayed emetic reactions induced by Cisplatin (HY-17394) in ferrets via acting on NK1 receptors in the central nervous system. Ezlopitant has the potential for pain, chemotherapy-induced emesis and irritable bowel syndrome research.

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

Ezlopitant Chemical Structure

Ezlopitant Chemical Structure

CAS No. : 147116-64-1

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Description

Ezlopitant (CJ-11,974) is a selective, non-peptidic neurokinin-1 (NK-1)-receptor antagonist. Ezlopitant inhibits both acute and delayed emetic reactions induced by Cisplatin (HY-17394) in ferrets via acting on NK1 receptors in the central nervous system. Ezlopitant has the potential for pain, chemotherapy-induced emesis and irritable bowel syndrome research[1][2][3].

In Vitro

Ezlopitant (CJ-11,974) is converted to two pharmacologically active metabolites: CJ-12458, an alkene metabolite and CJ-12764, a benzylic alcohol[2].

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

In Vivo

Ezlopitant (CJ-11,974; 2, 5, 10 mg/kg; i.p.; 30 minutes) decreases both sucrose and ethanol operant-self administration in rats[1].
Pharmacokinetic Parameters of Ezlopitant in Rat, Gerbil, Guinea pig, Ferret, Dog, Monkey [2].

Rat (IV; 1 mg/kg) Gerbil (IV; 1 mg/kg) Guinea pig (IV; 0.2 mg/kg) Ferret (SC; 0.8 mg/kg) Dog (IV; 1 mg/kg) Monkey (IV; 1 mg/kg)
Tmax (h) 5.3 0.3 0.3 0.9 0.8
Cmax (ng/mL) 18 5.98 106 5.98 198
AUC0-∞ (ng∗h/mL) 257 125 35.5 528 634 478
t1/2 (h) 7.7 2.9 0.6 2.2 2.5 5.0
CLp (mL/min/kg) 65 136 98 27 27 42
F (%) 15 2.1 17 28 2.7

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

Animal Model: Male, Long-Evans rats (233±2 g)[1]
Dosage: 2, 5 or 10 mg/kg
Administration: IP; single dose
Result: Attenuated the number of active lever presses for 5% sucrose.
Highest dose significantly inhibited operant self-administration of 10% ethanol compared with vehicle.
Molecular Weight

454.65

Formula

C31H38N2O

CAS No.
SMILES

COC(C=CC(C(C)C)=C1)=C1CN[C@@H](C2CCN3CC2)[C@@H]3C(C4=CC=CC=C4)C5=CC=CC=C5

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Room temperature in continental US; may vary elsewhere.

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

Purity & Documentation
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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Ezlopitant
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HY-106982
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