Pancuronium bromide
CAS No. 15500-66-0
Pancuronium bromide ( NSC 293162 )
产品货号. M12200 CAS No. 15500-66-0
Pancurium dibromide 是一种竞争性 AChR 拮抗剂 (IC50 = 5.5 nM),可作为骨骼肌松弛剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 25MG | ¥105 | 有现货 |
|
| 50MG | ¥138 | 有现货 |
|
| 100MG | ¥178 | 有现货 |
|
| 500MG | ¥413 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥212 | 有现货 |
|
生物学信息
-
产品名称Pancuronium bromide
-
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Pancurium dibromide 是一种竞争性 AChR 拮抗剂 (IC50 = 5.5 nM),可作为骨骼肌松弛剂。
-
产品描述Pancuronium dibromide is a competitive AChR antagonist (IC50 = 5.5 nM) and acts as a skeletal muscle relaxant. Pancuronium dibromide interrupts neuromuscular transmission by competing with acetylcholine for receptor sites on the motor end-plate. (In Vitro):The action of Pancuronium on transmembrane sodium conductance is investigated in dorsal root ganglion neurones of chick embryos. Externally perfused Pancuronium (50 μM to 1 mM) reversibly inhibits the current by a fast mechanism of action. Inhibition is concentration-dependent (with a half-effective dose of 170 μM) but not voltage-dependent. Pancuronium may reduce the sodium current by interacting with the sodium channels in both the resting and open states.(In Vivo):Pancuronium (0.5 mg/kg; intravenous injection) abolishes the bradycardia induced both by injected acetylcholine (ACh) and by vagal nerve stimulation in guinea-pigs (250-300 g, male). At doses which produce 100% neuromuscular blockade, Pancuronium (0.04 mg/kg) potentiates vagally-induced bronchoconstriction.Potentiation by Pancuronium of the effects of adrenergic nerve stimulation, is found in rat anococcygeus and vas deferens.
-
体外实验The action of Pancuronium on transmembrane sodium conductance is investigated in dorsal root ganglion neurones of chick embryos. Externally perfused Pancuronium (50 μM to 1 mM) reversibly inhibits the current by a fast mechanism of action. Inhibition is concentration-dependent (with a half-effective dose of 170 μM) but not voltage-dependent. Pancuronium may reduce the sodium current by interacting with the sodium channels in both the resting and open states.
-
体内实验Pancuronium (0.5 mg/kg; intravenous injection) abolishes the bradycardia induced both by injected acetylcholine (ACh) and by vagal nerve stimulation in guinea-pigs (250-300 g, male). At doses which produce 100% neuromuscular blockade, Pancuronium (0.04 mg/kg) potentiates vagally-induced bronchoconstriction. Potentiation by Pancuronium of the effects of adrenergic nerve stimulation, is found in rat anococcygeus and vas deferens.
-
同义词NSC 293162
-
通路Endocrinology/Hormones
-
靶点AChR
-
受体AChR| mAChR
-
研究领域Neurological Disease
-
适应症——
化学信息
-
CAS Number15500-66-0
-
分子量732.67
-
分子式C35H60Br2N2O4
-
纯度>98% (HPLC)
-
溶解度Very soluble in water
-
SMILESCC(=O)O[C@H]1C[C@@H]2CC[C@@H]3[C@@H]([C@]2(C[C@@H]1[N+]4(CCCCC4)C)C)CC[C@]5([C@H]3C[C@@H]([C@@H]5OC(=O)C)[N+]6(CCCCC6)C)C.[Br-].[Br-]
-
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.Stovner J, et al. Br J Anaesth. 1975 Sep;47(9):949-54.
产品手册
关联产品
-
VU0238429
VU0238429 是毒蕈碱乙酰胆碱受体亚型 5(mAChR5 或 M5)的正变构调节剂(EC50:1.16 μM)。
-
Adenosine 5'-monopho...
单磷酸腺苷 (AMP) 也称为 5'-腺苷酸,是一种用作 RNA 单体的核苷酸。
-
Solifenacin
Solifenacin (YM905 free base) 是一种新型毒蕈碱受体拮抗剂,其对 M1、M2 和 M3 受体的 pK 分别为 7.6、6.9 和 8.0。
021-51111890
购物车()
sales@molnova.cn

