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三碘季胺酚 /Gallamine Triethiodide 98%

货号:A616170 同义名: 加拉碘铵 / Gallamine (iodide) Ambeed 开学季,买赠积分,赢豪礼

Gallamine triethiodide is a competitive cholinergic receptor blocker with an IC50 of 68.0 ± 8.4 μM, used as a non-depolarising muscle relaxant.

Gallamine Triethiodide 化学结构 CAS号:65-29-2
Gallamine Triethiodide 化学结构
CAS号:65-29-2
Gallamine Triethiodide 3D分子结构
CAS号:65-29-2
Gallamine Triethiodide 化学结构 CAS号:65-29-2
Gallamine Triethiodide 3D分子结构 CAS号:65-29-2
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Gallamine Triethiodide 纯度/质量文件 产品仅供科研

货号:A616170 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。

Gallamine Triethiodide 生物活性

靶点
  • AChR

    AChR, IC50:68.0 μM

描述 Gallamine Triethiodine is a cholinergic receptor inhibitor. It acts by combining with the cholinergic receptor sites in muscle and competitively blocking the transmitter action of acetylcholine. Gallamine triethiodide has a parasympatholytic effect on the cardiac vagus nerve which causes tachycardia and occasionally hypertension. Very high doses cause histamine release[3]. Internal gallamine triethiodide modifies Na+ channel kinetics in Myxicola axons but does not alter K+ conductance[4]. Slight accumulation of gallamine was noted in two of the four patients with biliary disease receiving multiple doses of gallamine, but this was also characteristic of data obtained in the patients without obstruction[5].

Gallamine Triethiodide 参考文献

[1]Abbas MN, Mostafa GA. Gallamine-tetraphenylborate-modified carbon paste electrode for the potentiometric determination of gallamine triethiodide(flaxedil). J Pharm Biomed Anal. 2003 Mar 26;31(4):819-26.

[2]Nedoma J, Tucek S, et al. Stabilization of antagonist binding to cardiac muscarinic acetylcholine receptors by gallamine and other neuromuscular blocking drugs. J Pharmacol Exp Ther. 1986 Jan;236(1):219-23.

[3]SMITH RH, THOMAS DL. Gallamine triethiodide as an adjunct to electroplexy. Br Med J. 1951 Apr 21;1(4711):860-2.

[4]Schauf CL, Smith KJ. Gallamine triethiodide-induced modifications of sodium conductance in Myxicola giant axons. J Physiol. 1982 Feb;323:157-71.

[5]Ramzan IM, Shanks CA, Triggs EJ. Pharmacokinetics and pharmacodynamics of gallamine triethiodide in patients with total biliary obstruction. Anesth Analg. 1981 May;60(5):289-96.

Gallamine Triethiodide 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.12mL

0.22mL

0.11mL

5.61mL

1.12mL

0.56mL

11.22mL

2.24mL

1.12mL

Gallamine Triethiodide 技术信息

CAS号65-29-2
分子式C30H60I3N3O3
分子量 891.529
别名 加拉碘铵 ;Gallamine (iodide)
运输蓝冰
存储条件

粉末 Keep in dark place,Inert atmosphere,2-8°C

液体 -20°C:1个月-80°C:12个月

溶解度

H2O: 30 mg/mL(33.65 mM)

动物实验配方
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