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泮库溴铵 /Pancuronium dibromide 98%

货号:A737050 同义名: Pavulon Ambeed 开学季,买赠积分,赢豪礼

Pancuronium dibromide is a competitive nAchR antagonist, causing skeletal muscle relaxation and paralysis through competitively binding to the nicotinic receptor at the neuromuscular junction.

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Pancuronium dibromide 化学结构 CAS号:15500-66-0
Pancuronium dibromide 化学结构
CAS号:15500-66-0
Pancuronium dibromide 3D分子结构
CAS号:15500-66-0
Pancuronium dibromide 化学结构 CAS号:15500-66-0
Pancuronium dibromide 3D分子结构 CAS号:15500-66-0
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Pancuronium dibromide 纯度/质量文件 产品仅供科研

货号:A737050 标准纯度: 98%
批次查询: 批次纯度:

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产品名称 AChE AChR mAChR nAChR 其他靶点 纯度
Donepezil +++

bAChE, IC50: 8.12 nM

hAChE, IC50: 11.6 nM

98%
Loganin ++

AChE, IC50: 3.95 μM

99%+
topride HCl ++

AChE, IC50: 2.04 μM

98%
Dehydroevodiamine HCl 99%+
Jatrorrhizine ++

AChE, IC50: 872 nM

99%+
Palmatine ++

AChE, IC50: 0.51 μM

98%
(-)-Huperzine A ++++

AChE (G4 form), Ki: 7 nM

98%
Galanthamine HBr ++

AChE, IC50: 0.35 μM

98%
Trospium chloride 99%
Tiotropium Bromide Monohydrate 98+%
Gallamine Triethiodide +

AChR, IC50: 68.0 μM

98%
Hexamethonium Bromide 99%
Pancuronium dibromide 98%
Neostigmine bromide 98%
Orphenadrine citrate 98%
Oxybutynin 98%
Irsogladine PDE 98%
Pyridostigmine bromide 99+%
Rivastigmine +

AChR, IC50: 5.5 μM

98%
Paroxetine hydrochloride 97%
Rocuronium Bromide 98%
Tropicamide +++

M4 mAChR, IC50: 8 nM

98%
Diphenmanil methylsulfate 98%
Umeclidinium bromide 95%
Otilonium bromide 98%
Flavoxate HCl +

mAChR, IC50: 12.2 μM

98%
Ipratropium bromide 98%
Diphenidol HCl 98%
Darifenacin hydrobromide ++++

M3 mAChR, pKi: 8.9

98%
Aclidinium Bromide ++++

M4 mAChR, Ki: 0.21 nM

M2 mAChR, Ki: 0.1 nM

98%
Oxybutynin chloride 99%
Pentoxyverine citrate 98%
Solifenacin 98%
Catharanthine 98%
Benzethonium chloride +++

α7 nAChRs, IC50: 122 nM

α4β2 nAChRs, IC50: 49 nM

99+%
Vinblastine sulfate +

nAChR, IC50: 8.9 μM

99%
PNU-120596 ++

α7 nAChR, EC50: 216 nM

99+%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Pancuronium dibromide 生物活性

靶点
  • AChR

描述 Pancuronium Dibromide is a competitive AChR antagonist.Pancuronium (10 mg/kg ) reduced ACh-induced bronchoconstriction. At doses which produce 100% neuromuscular blockade, both pancuronium (0.04 mg/kg) and gallamine (4 mg/kg) potentiated vagally-induced bronchoconstriction[3].Competitive block of embryonic-type nicotinic acetylcholine receptor channels by pancuronium or atracurium after preincubation of outside-out patches with the respective blocker[4]. Moreover, Pancuronium may reduce the sodium current by interacting with the sodium channels in both the resting and open states[5].

Pancuronium dibromide 参考文献

[1]Lowenick CV, Krampfl K, et al. Open channel and competitive block of nicotinic receptors by pancuronium and atracurium. Eur J Pharmacol. 2001 Feb 9;413(1):31-5.

[2]Melnikov AL, Malakhov KY, et al. Cardiac effects of non-depolarizing neuromuscular blocking agents pancuronium,vecuronium, and rocuronium in isolated rat atria. Gen Pharmacol. 1999 Oct;33(4):313-7.

[3]Fryer AD, Maclagan J. Pancuronium and gallamine are antagonists for pre- and post-junctional muscarinic receptors in the guinea-pig lung. Naunyn Schmiedebergs Arch Pharmacol. 1987 Apr;335(4):367-71.

[4]Löwenick CV, Krampfl K, Schneck H, Kochs E, Bufler J. Open channel and competitive block of nicotinic receptors by pancuronium and atracurium. Eur J Pharmacol. 2001 Feb 9;413(1):31-5.

[5]Maestrone E, Magnelli V, Nobile M, Usai C. Extracellular pancuronium affects sodium current in chick embryo sensory neurones. Br J Pharmacol. 1994 Jan;111(1):283-7.

Pancuronium dibromide 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.36mL

0.27mL

0.14mL

6.82mL

1.36mL

0.68mL

13.65mL

2.73mL

1.36mL

Pancuronium dibromide 技术信息

CAS号15500-66-0
分子式C35H60Br2N2O4
分子量 732.67
别名 Pavulon
运输蓝冰
存储条件

粉末 Keep in dark place,Inert atmosphere,Room temperature

液体 -20°C:3-6个月-80°C:12个月

溶解度

DMSO: 105 mg/mL(143.31 mM),注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

H2O: 100 mg/mL(136.49 mM),配合低频超声助溶

动物实验配方
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