1. Membrane Transporter/Ion Channel Neuronal Signaling GPCR/G Protein
  2. Calcium Channel 5-HT Receptor
  3. Levemopamil

Levemopamil 是一种钙通道阻滞剂及 5-HT2 受体拮抗剂。Levemopamil 可对缺血性急性肾损伤发挥肾脏保护作用。Levemopamil 可用于缺血性急性肾衰竭的相关研究。

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Levemopamil

Levemopamil Chemical Structure

CAS No. : 101238-51-1

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Levemopamil is a calcium channel blocker and 5-HT2 receptor antagonist. Levemopamil exerts renoprotective effects against ischemic acute kidney injury. Levemopamil is applicable to research related to ischemic acute renal failure[1].

体内研究
(In Vivo)

Levemopamil (6 mg/kg/h;静脉注射;持续输注 7 h) 可在大鼠少尿型缺血性急性肾损伤模型中短暂将少尿转变为非少尿,维持低水平肾小球滤过功能,并保护皮质线粒体 ATP 的合成[1]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Sprague-Dawley (female, adult, 191-239 g, left unilateral renal artery occlusion for 1 hour followed by 6 hours of reperfusion/reflow)[1]
Dosage: 6 mg/kg/h
Administration: i.v.; continuous infusion; from 1 hour before ischaemia until 6 hours after reflow
Result: Significantly increased urine flow and maintained measurable endogenous creatinine clearance in the ischaemic left kidney at 2 and 6 h of reperfusion.
Largely preserved mitochondrial ATP synthesis and normal ADP/O ratio.
Slightly attenuated the rise in cortical mitochondrial calcium content.
分子量

334.50

Formula

C23H30N2

CAS 号
中文名称

左依莫帕米

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
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  • 稀释计算器

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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Levemopamil
目录号:
HY-113581
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