• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号

Rocuronium bromide

CAS No. 119302-91-9

Rocuronium bromide ( (+)-Rocuronium )

产品货号. M10670 CAS No. 119302-91-9

罗库溴铵(快速起效-库溴铵)是维库溴铵的去乙酰氧基类似物,起效更快。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
10MG ¥394 有现货
50MG ¥542 有现货
100MG ¥714 有现货
200MG ¥896 有现货
500MG ¥1281 有现货
1G 获取报价 有现货
1 mL x 10 mM in DMSO ¥434 有现货

生物学信息

  • 产品名称
    Rocuronium 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
    罗库溴铵(快速起效-库溴铵)是维库溴铵的去乙酰氧基类似物,起效更快。
  • 产品描述
    Rocuronium (rapid onset-curonium) is a desacetoxy analogue of vecuronium with a more rapid onset of action. It is an aminosteroid non-depolarizing neuromuscular blocker or muscle relaxant used in modern anaesthesia, to facilitate endotracheal intubation and to provide skeletal muscle relaxation during surgery or mechanical ventilation.Introduced in 1994, rocuronium has rapid onset, and intermediate duration of action. It is marketed under the trade name of Zemuron in the United States and Esmeron in most other countries.(In Vitro):Rocuronium reduced the indirectly elicited twitch tensions in normal (50% inhibitory concentration [IC(50)], 9.84 [9.64-10.04] μM, mean [95% confidence interval]) and all pretreated diaphragms (P < .01, n = 6) in a concentration-dependent fashion . The ED95 of rocuronium is essentially the same for children as for adults. Its duration of action is similar to vecuronium, and it is shorter for children than for adults. Rocuronium is readily reversed with conventional doses of cholinesterase-inhibiting drugs . Onset time until maximum block, duration until 25% recovery of twitch height, and recovery from 25 until 75% of twitch height were 1.7 (32), 53 (19) and 20 (37) min, respectively .(In Vivo):Only 8.7±5.7% (SD) and 6.0±2.8% of an injected dose of ORG 9426 and ORG 9616 was excreted into the urine, respectively. Conversely, 54.4±9.2% and 52.4±9.2% of an injected dose of ORG 9426 and 35.7±12.2% and 46.8±9.7% of ORG 9616 were excreted into the bile in cats without and with renal pedicle ligation, respectively .
  • 体外实验
    Rocuronium reduced the indirectly elicited twitch tensions in normal (50% inhibitory concentration [IC(50)], 9.84 [9.64-10.04] μM, mean [95% confidence interval]) and all pretreated diaphragms (P < .01, n = 6) in a concentration-dependent fashion . The ED95 of rocuronium is essentially the same for children as for adults. Its duration of action is similar to vecuronium, and it is shorter for children than for adults. Rocuronium is readily reversed with conventional doses of cholinesterase-inhibiting drugs . Onset time until maximum block, duration until 25% recovery of twitch height, and recovery from 25 until 75% of twitch height were 1.7 (32), 53 (19) and 20 (37) min, respectively .
  • 体内实验
    Only 8.7±5.7% (SD) and 6.0±2.8% of an injected dose of ORG 9426 and ORG 9616 was excreted into the urine, respectively. Conversely, 54.4±9.2% and 52.4±9.2% of an injected dose of ORG 9426 and 35.7±12.2% and 46.8±9.7% of ORG 9616 were excreted into the bile in cats without and with renal pedicle ligation, respectively .
  • 同义词
    (+)-Rocuronium
  • 通路
    Endocrinology/Hormones
  • 靶点
    AChR
  • 受体
    mAChR
  • 研究领域
    Neurological Disease
  • 适应症
    ——

化学信息

  • CAS Number
    119302-91-9
  • 分子量
    609.68
  • 分子式
    C32H53BrN2O4
  • 纯度
    >98% (HPLC)
  • 溶解度
    Ethanol: 122 mg/mL (200.1 mM); Water: 122 mg/mL (200.1 mM); DMSO: 122 mg/mL (200.1 mM)
  • SMILES
    CC(=O)O[C@H]1[C@H](C[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC[C@@H]4[C@@]3(C[C@@H]([C@H](C4)O)N5CCOCC5)C)C)[N+]6(CCCC6)CC=C.[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. Jonsson Fagerlund M, et al. Anesthesiology. 2009 Jun;110(6):1244-52.
产品手册
关联产品
  • JHU 37152

    JHU 37152 是一种仅由设计药物 (DREADD) 激动剂激活的设计受体,体外人毒蕈碱乙酰胆碱 M3 受体 (hM3Dq) 和 hM4Di 的 Ki 值分别为 1.8 nM 和 8.7 nM。

  • Pirenzepine dihydroc...

    一种抗毒蕈碱剂,其抑制胃分泌的剂量低于影响胃肠道运动、唾液、中枢神经系统、心血管、眼和泌尿功能所需的剂量。

  • N-p-trans-Coumaroylt...

    Np-trans-Coumaroyltyramine 是一种天然产物,是一种乙酰胆碱酯酶 (AChE) 抑制剂,IC50 为 122 μM。 Np-trans-Coumaroyltyramine 表现出抗锥虫活性,对 T. brucei rhodesense 的 IC50 为 13.3 μM。