Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Selective vasopressin V1A receptor antagonist. Inhibits vasopressin and oxytocin-induced increases in intracellular calcium concentrations in vitro (IC50 values are 5 and 30 nM respectively). Exhibits potent and prolonged antivasopressor activity and induces anxiolytic-like effects in the dorsal, but not ventral, hippocampus in vivo.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
10 mg | Inquiry | $ 402.00 |
Description | Selective vasopressin V1A receptor antagonist. Inhibits vasopressin and oxytocin-induced increases in intracellular calcium concentrations in vitro (IC50 values are 5 and 30 nM respectively). Exhibits potent and prolonged antivasopressor activity and induces anxiolytic-like effects in the dorsal, but not ventral, hippocampus in vivo. |
Molecular Weight | 1151.38 |
Formula | C52H74N14O12S2 |
CAS No. | 73168-24-8 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
H2O: 2 mg/mL
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(d(CH2)51,Tyr(Me)2,Arg8)-Vasopressin 73168-24-8 (d(CH2)51,Tyr(Me)2,Arg8)Vasopressin (d(CH2)51,Tyr(Me)2,Arg8) Vasopressin (d(CH-2)51,Tyr(Me)2,Arg8)-Vasopressin inhibitor inhibit