Vecuronium bromide
CAS No. 50700-72-6
Vecuronium bromide ( NC 45 )
产品货号. M14731 CAS No. 50700-72-6
维库溴铵(溴化物)是一种非去极化阻断剂类别的肌肉松弛剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥125 | 有现货 |
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| 5MG | ¥183 | 有现货 |
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| 10MG | ¥253 | 有现货 |
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| 25MG | ¥423 | 有现货 |
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| 50MG | ¥616 | 有现货 |
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| 100MG | ¥873 | 有现货 |
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| 500MG | ¥2142 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥265 | 有现货 |
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生物学信息
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产品名称Vecuronium bromide
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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
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产品简述维库溴铵(溴化物)是一种非去极化阻断剂类别的肌肉松弛剂。
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产品描述Vecuronium (bromide) is a muscle relaxant in the category of non-depolarizing blocking agents.(In Vitro):Vecuronium bromide (0-100 μM, 15 min) inhibits [3H] norepinephrine (NE) uptake to 65% at 100 μM in adrenal medullary cells.Vecuronium bromide (0-15 μM,72 hours) inhibits cancer cell proliferation and migration in a concentration-dependent manner.Vecuronium bromide (0-15 μM,72 hours) can significantly reduce cell viability by combining with cisplatin.(In Vivo):Vecuronium bromide (Intravenous injection, 0-5 μM, every 30 min, 2 hours) attenuates the response of carotid sinus nerve activity (CSNA) to hypoxia in a dose-dependent manner and inhibits the neural response of the carotid body to acetylcholine (ACh) in Wister rats.
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体外实验Vecuronium bromide (0-100 μM, 15 min) inhibits [3H] norepinephrine (NE) uptake to 65% at 100 μM in adrenal medullary cells.Vecuronium bromide (0-15 μM,72 hours) inhibits cancer cell proliferation and migration in a concentration-dependent manner.Vecuronium bromide (0-15 μM,72 hours) can significantly reduce cell viability by combining with cisplatin.Cell Proliferation Assay Cell Line:Lung cancer cell line (A549)Concentration:0-15 μM Incubation Time:72 hours Result:Inhibited cell proliferation at concentrations ranging from 5.0 μM to 15 μM.Cell Cytotoxicity Assay Cell Line:Lung cancer cell line (A549)Concentration:0-15 μM Incubation Time:72 hours Result:Resulted in a decrease in cell viability from 10 μM to 15 Μm by combining with cisplatin.
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体内实验Vecuronium bromide (Intravenous injection, 0-5 μM, every 30 min, 2 hours) attenuates the response of carotid sinus nerve activity (CSNA) to hypoxia in a dose-dependent manner and inhibits the neural response of the carotid body to acetylcholine (ACh) in Wister rats. Animal Model:Wister rats weighing 250-350 gDosage:0-5 μM Administration:Intravenous injection; every 30 min; 2 hours Result:Significantly diminished CSNA response to hypoxia at the concentration of 5 μM and reduced carotid sinus nerve response to ACh at 0.5 μM.
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同义词NC 45
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通路Endocrinology/Hormones
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靶点AChR
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受体nAChR
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研究领域Neurological Disease
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适应症——
化学信息
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CAS Number50700-72-6
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分子量637.73
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分子式C34H57BrN2O4
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纯度>98% (HPLC)
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溶解度Ethanol: 100 mg/mL (156.8 mM); Water: 4 mg/mL (6.27 mM); DMSO: 100 mg/mL (156.8 mM)
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SMILESCC(O[C@@H]1[C@@H](N2CCCCC2)C[C@]3(C)[C@@]4([H])CC[C@]5(C)[C@H](OC(C)=O)[C@@H]([N+]6(C)CCCCC6)C[C@@]5([H])[C@]4([H])CC[C@@]3([H])C1)=O.[Br-]
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化学全称1-((2S,3S,5S,8R,9S,10S,13S,14S,16S,17S)-3,17-diacetoxy-10,13-dimethyl-2-(piperidin-1-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-16-yl)-1-methylpiperidin-1-ium bromide
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Jonsson Fagerlund M, et al. Anesthesiology. 2009 Jun;110(6):1244-52.
产品手册
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