021-51111890
购物车（）
sales@molnova.cn
Bretylium tosylate
CAS No. 61-75-6
Bretylium tosylate ( —— )
产品货号. M20751 CAS No. 61-75-6
Bretylium tosylate is an inhibitor of the presynaptic release of vasoconstrictor neurotransmitters a available antiarrhythmic drug for ventricular arrhythmias.
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ￥300 | 有现货 |
|
| 5MG | ￥478 | 有现货 |
|
| 10MG | ￥737 | 有现货 |
|
| 25MG | ￥964 | 有现货 |
|
| 50MG | ￥1215 | 有现货 |
|
| 100MG | ￥1450 | 有现货 |
|
| 200MG | ￥2236 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Bretylium tosylate
-
注意事项本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断
-
产品简述Bretylium tosylate is an inhibitor of the presynaptic release of vasoconstrictor neurotransmitters a available antiarrhythmic drug for ventricular arrhythmias.
-
产品描述Bretylium tosylate is an inhibitor of the presynaptic release of vasoconstrictor neurotransmitters a available antiarrhythmic drug for ventricular arrhythmias.
-
同义词——
-
通路Others
-
靶点Other Targets
-
受体Others
-
研究领域Others
-
适应症xerophthalmia
化学信息
-
CAS Number61-75-6
-
分子量414.36
-
分子式C18H24BrNO3S
-
纯度>98% (HPLC)
-
溶解度DMSO:30 mg/mL (72.40 mM)
-
SMILESCC1=CC=C(C=C1)S([O-])(=O)=O.CC[N+](C)(C)CC1=CC=CC=C1Br
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1.Dhurandhar R W Teasdale S J Mahon W A . Bretylium Tosylate in the Management of Refractory Ventricular Fibrillation[J]. Canadian Medical Association journal 1971 105(2):161-5 passim.
产品手册
关联产品
-
BAY 2416964
BAY 2416964 is a potent and orally active aryl hydrocarbon receptor (AHR) antagonist extracted from patent WO2018146010A1 (example 192, IC50: 341 nM). It has the potential for cancer treatment.BAY 2416964 induces AHR-regulated gene CYP1A1 expression in human monocytic U937 cells (IC50: 4.3 nM).
-
BI-6C9
BI-6C9 is an inhibitor of tBid (Kd = 20 μM).BI-6c9 prevented MOMP and mitochondrial fission and protected the cells from cell death.
-
Kushenol A
Kushenol A is a kind of Adenosine 3', 5'-cyclic monophosphate(cAMP)phosphodiesterase inhibitiors, it shows selective alpha-glucosidase inhibitory activity.
