产品
编 号：F330675
分子式：C27H34N4O3
分子量：462.58
分子式：C27H34N4O3
分子量：462.58
产品类型
规格
价格
是否有货
10mM*1mL in DMSO
询价
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5mg
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10mg
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50mg
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结构图
CAS No: 347887-36-9
产品详情
生物活性：
Fedovapagon (VA106483) is a selective and orally active vasopressin V2 receptor (V2R) agonist with an EC50 of 24 nM. Fedovapagon can be used in the research of nocturia.
体内研究：
Fedovapagon (1 mg/kg, oral administration) inhibits urine output with 81% inhibition rate in rats.Animal Model:Brattleboro rats
Dosage:1 mg/kg, 3 mg/kg
Administration:Oral administration
Result:Reduced urine volume with almost full inhibition of urine output for 2 h.Returned the urine to normal levels 5 h after dosing.
Fedovapagon (VA106483) is a selective and orally active vasopressin V2 receptor (V2R) agonist with an EC50 of 24 nM. Fedovapagon can be used in the research of nocturia.
体内研究：
Fedovapagon (1 mg/kg, oral administration) inhibits urine output with 81% inhibition rate in rats.Animal Model:Brattleboro rats
Dosage:1 mg/kg, 3 mg/kg
Administration:Oral administration
Result:Reduced urine volume with almost full inhibition of urine output for 2 h.Returned the urine to normal levels 5 h after dosing.
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