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Merck
CN

SML2907

Sigma-Aldrich

Azumolene

≥98% (HPLC)

别名:

1-[[[5-(4-Bromophenyl)-2-oxazolyl]methylene]amino]-2,4-imidazolidinedione, EU 4093

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关于此项目

经验公式(希尔记法):
C13H9BrN4O3
化学文摘社编号:
分子量:
349.14
MDL编号:
UNSPSC代码:
12352200
NACRES:
NA.77
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质量水平

方案

≥98% (HPLC)

表单

powder

颜色

white to very dark gray

溶解性

DMSO: 2 mg/mL, clear

储存温度

−20°C

InChI

1S/C13H9BrN4O3/c14-9-3-1-8(2-4-9)10-5-15-12(21-10)6-16-18-7-11(19)17-13(18)20/h1-6H,7H2,(H,17,19,20)

InChI key

SEGCNGONCZQFDW-UHFFFAOYSA-N

生化/生理作用

Azumolene, a more water-soluble analog of dantrolene, is a potent inhibitor of sarcoplasmic reticulum (SR) ryanodine receptor (RyR) that inhibits skeletal muscle SR Ca2+ release. Azumolene is a direct acting skeletal muscle relaxant that induces effective blockade of skeletal muscle RyR1.
potent inhibitor of sarcoplasmic reticulum ryanodine receptor

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Daoyuan Si et al.
Journal of cardiovascular electrophysiology, 29(12), 1707-1715 (2018-09-12)
Following long-duration ventricular fibrillation (LDVF), reinitiation of ventricular fibrillation (VF) poses a major challenge during resuscitation. Ryanodine receptor 2 (RyR2) becomes dysfunctional following VF. The relationship between LDVF, RyR2 modulation, and ventricular refibrillation, as well as the role of RyR2 phosphorylation
Yingfan Zhang et al.
The Journal of pharmacology and experimental therapeutics, 314(1), 94-102 (2005-04-16)
Azumolene is an analog of dantrolene, the only approved medicine for treatment of malignant hyperthermia (MH). The pharmacological mechanism of these drugs is to inhibit skeletal muscle sarcoplasmic reticulum (SR) Ca2+ release by modulating the activity of the SR ryanodine
Erin E Talbert et al.
PloS one, 11(2), e0148161-e0148161 (2016-02-06)
Mechanical ventilation (MV) is a life-saving intervention for patients in respiratory failure. However, prolonged MV causes the rapid development of diaphragm muscle atrophy, and diaphragmatic weakness may contribute to difficult weaning from MV. Therefore, developing a therapeutic countermeasure to protect

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