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- 详细信息
- 技术资料
- 保存条件:
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 英文名:
RDEA594
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
878672-00-5
- 规格:
10 mM * 1 mL/5 mg/10 mg/50 mg/100 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥605.0 |
|---|---|---|---|
| 规格: | 5 mg | 产品价格: | ¥550.0 |
| 规格: | 10 mg | 产品价格: | ¥700.0 |
| 规格: | 50 mg | 产品价格: | ¥1900.0 |
| 规格: | 100 mg | 产品价格: | ¥2300.0 |
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Lesinurad
CAS No. : 878672-00-5
MCE 国际站:Lesinurad
产品活性:Lesinurad 是一种 URAT1 和 OAT 抑制剂,用作肾转运蛋白OAT1 和OAT3 的底物,Km值分别为 0.85 和 2 μM。
研究领域:Membrane Transporter/Ion Channel
作用靶点:URAT1
In Vitro: Lesinurad is a novel selective uric acid reabsorption inhibitor (SURI). Lesinurad is determined to be a substrate for the kidney transporters organic anion transporter (OAT1) and OAT3 with Km values of 0.85 and 2 μM, respectively. Lesinurad (RDEA594) is a URAT1 and OAT inhibitor, which increases proximal renal tubule urate excretion. Lesinurad (RDEA594) is a potential uric acid lowering agent througn inhibition of uric acid reuptake, and exhibits favorable p450 profiles, inhibits CYP2C9 and CYP2C8 with IC50 of 14.4 μM and 16.2 μM, respectively. IC50s of Lesinurad are all above 100 μM for CYP1A2, CYP2C19,and CYP2D6.
In Vivo: Lesinurad (RDEA594) shows better pharmacokinetics than its pro-drug RDEA806. The 100 mg dose of Lesinurad exhibits a phamacological effect in the range of that produced by 300 mg to 800 mg single doses of RDEA806.
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