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- 详细信息
- 技术资料
- 保存条件:
4°C, sealed storage, away from moisture
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
132866-11-6
- 规格:
10 mM * 1 mL/10 mg/25 mg/50 mg/100 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥489.0 |
|---|---|---|---|
| 规格: | 10 mg | 产品价格: | ¥445.0 |
| 规格: | 25 mg | 产品价格: | ¥933.0 |
| 规格: | 50 mg | 产品价格: | ¥1494.0 |
| 规格: | 100 mg | 产品价格: | ¥2391.0 |
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Lercanidipine hydrochloride
CAS No. : 132866-11-6
MCE 国际站:Lercanidipine hydrochloride
产品活性:Lercanidipine 是第三代、亲脂性、可穿透血脑屏障、血管选择性、具有口服活性的二氢吡啶钙通道阻断剂,pIC50 为 7.74(由 微摩尔浓度 转换而来)。Lercanidipine 具有持久的降压作用以及肾脏和神经保护作用,还具有抗氧化、抗炎和抗凋亡的特性。Lercanidipine 可用于心血管和神经学研究。
研究领域:Membrane Transporter/Ion Channel | Neuronal Signaling | Apoptosis | NF-κB | Metabolic Enzyme/Protease | Immunology/Inflammation | MAPK/ERK Pathway
作用靶点:Calcium Channel | Apoptosis | Reactive Oxygen Species | p38 MAPK | NF-κB
In Vitro: Lercanidipine (1, 10 μM, 24 h) exerts suppression of NO, ROS and TNF-a through down-regulation of iNOS, MMP-2/MMP-9, and HMGB1, as well as inhibition of MAPKs, Akt/IkB-a and NF-kB pathways in LPS/IFN-γ-induced VSMCs.
In Vivo: Lercanidipine (1, 0.5 and 0.25 mg/kg, i.p., acute administration) significantly reduces neurological deficit score, motor deficits and cerebral infarction volume in the MCAo model rats.
Lercanidipine (1.92-0.12 mg/kg, p.o., acute administration) lowers blood pressure effectively and dose-dependently in spontaneous hypertensive rats.
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