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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:
DuP 996
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
105431-72-9
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥836.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥380.0 |
| 规格: | 5 mg | 产品价格: | ¥971.0 |
| 规格: | 10 mg | 产品价格: | ¥1563.0 |
| 规格: | 25 mg | 产品价格: | ¥2934.0 |
| 规格: | 50 mg | 产品价格: | ¥4694.0 |
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Linopirdine
CAS No. : 105431-72-9
MCE 国际站:Linopirdine
产品活性:Linopirdine (DuP 996) 是一种具有口服活性的,选择性 M 型 K+ 电流 (IM;Kv7;KCNQ Channels) 抑制剂,IC50 为 2.4 μM。Linopirdine 是 TRPV1 激活剂。Linopirdine 是一种公认的认知增强活性分子,可增加大鼠脑组织中乙酰胆碱的释放。
研究领域:Membrane Transporter/Ion Channel | Neuronal Signaling
作用靶点:Potassium Channel | TRP Channel
In Vitro: Linopirdine (DuP 996) inhibits IC (measured as a medium afterhyperpolarization tail current, ImAHP) with an IC50 of 16.3 μM. Linopirdine (100 μM) weakly inhibits the K+ leak current, IL, the transient outward current, IA, the delayed rectifier, IK, and the slow component of IAHP, by 28, 37, 36 and 52 percent, respectively. The mixed Na+/K+ inward rectifying current, IQ, is essentially unaffected by Linopirdine (IC50>300 μM).
?Linopirdine acts as an agonist of TRPV1 (transient receptor potential vanilloid type 1).
In Vivo: Linopirdine (DuP 996; i.v.; 0.1-6 mg/kg; increasing doses) transiently (10-15 min) and dose-dependently increases MAP by up to 15%.
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