Fedovapagon
CAS No. 347887-36-9
Fedovapagon ( —— )
产品货号. M33357 CAS No. 347887-36-9
Fedovapagon (VA106483) 是一种选择性的加压素 V2 受体 (V2R) 激动剂,EC50 值为24 nM。Fedovapagon 可用于夜尿症的研究。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥847 | 有现货 |
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| 10MG | ¥1311 | 有现货 |
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| 25MG | ¥2213 | 有现货 |
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| 50MG | ¥3274 | 有现货 |
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| 100MG | ¥4428 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥881 | 有现货 |
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生物学信息
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产品名称Fedovapagon
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Fedovapagon (VA106483) 是一种选择性的加压素 V2 受体 (V2R) 激动剂,EC50 值为24 nM。Fedovapagon 可用于夜尿症的研究。
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产品描述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.
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体外实验——
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体内实验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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同义词——
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通路GPCR/G Protein
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靶点Vasopressin Receptor
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受体Vasopressin Receptor
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研究领域——
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适应症——
化学信息
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CAS Number347887-36-9
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分子量462.58
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分子式C27H34N4O3
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO 中的溶解度 : ≥ 125 mg/mL (270.22 mM )
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SMILES[H][C@]1(CCCN1C(=O)NCc1ccc(cc1C)C(=O)N1CCCCc2ccccc12)C(=O)N(C)C
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Yea CM, et al.New benzylureas as a novel series of potent, nonpeptidic vasopressin V2 receptor agonists. J Med Chem. 2008 Dec 25;51(24):8124-34.?
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