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                同义名:
                    
                        
                            顺苯磺酸阿曲库铵
                            
                             / 51W89 besylate; Cisatracurium besilate
                            
                        
                    
                
                
                
                    
                     
                
            
Cisatracurium besylate 是一种非去极化神经肌肉阻断剂,能通过抑制神经肌肉的传递拮抗乙酰胆碱的效用。
 
                                 
                                
                            

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| 产品名称 | AChE ↓ ↑ | AChR ↓ ↑ | mAChR ↓ ↑ | nAChR ↓ ↑ | 其他靶点 | 纯度 | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Donepezil | +++ bAChE, IC50: 8.12 nM hAChE, IC50: 11.6 nM | 98% | |||||||||||||||||
| Loganin | ++ AChE, IC50: 3.95 μM | 99%+ | |||||||||||||||||
| topride HCl | ++ AChE, IC50: 2.04 μM | 98% | |||||||||||||||||
| Dehydroevodiamine HCl | ✔ | 99%+ | |||||||||||||||||
| Jatrorrhizine | ++ AChE, IC50: 872 nM | 99%+ | |||||||||||||||||
| Palmatine | ++ AChE, IC50: 0.51 μM | 95% | |||||||||||||||||
| (-)-Huperzine A | ++++ AChE (G4 form), Ki: 7 nM | 98% | |||||||||||||||||
| Galanthamine HBr | ++ AChE, IC50: 0.35 μM | 98% | |||||||||||||||||
| Trospium chloride | ✔ | 99% | |||||||||||||||||
| Tiotropium Bromide Monohydrate | ✔ | 97% | |||||||||||||||||
| Gallamine Triethiodide | + AChR, IC50: 68.0 μM | 98% | |||||||||||||||||
| Hexamethonium Bromide | ✔ | 99% | |||||||||||||||||
| Pancuronium dibromide | ✔ | 98% | |||||||||||||||||
| Neostigmine bromide | ✔ | 98% | |||||||||||||||||
| Orphenadrine citrate | ✔ | 98% | |||||||||||||||||
| Oxybutynin | ✔ | 98% | |||||||||||||||||
| Irsogladine | ✔ | PDE | 99% | ||||||||||||||||
| Pyridostigmine bromide | ✔ | 99+% | |||||||||||||||||
| Rivastigmine | + AChR, IC50: 5.5 μM | 98% | |||||||||||||||||
| Paroxetine HCl | ✔ | 99% | |||||||||||||||||
| Rocuronium Bromide | ✔ | 98% | |||||||||||||||||
| Tropicamide | +++ M4 mAChR, IC50: 8 nM | 98% | |||||||||||||||||
| Diphenmanil methylsulfate | ✔ | 97% | |||||||||||||||||
| Umeclidinium bromide | ✔ | 95% | |||||||||||||||||
| Otilonium bromide | ✔ | 98% | |||||||||||||||||
| Flavoxate HCl | + mAChR, IC50: 12.2 μM | 99% | |||||||||||||||||
| Ipratropium bromide | ✔ | 98% | |||||||||||||||||
| Diphenidol HCl | ✔ | 98% | |||||||||||||||||
| Darifenacin hydrobromide | ++++ M3 mAChR, pKi: 8.9 | 98% | |||||||||||||||||
| Aclidinium Bromide | ++++ M2 mAChR, Ki: 0.1 nM M4 mAChR, Ki: 0.21 nM | 98% | |||||||||||||||||
| Oxybutynin chloride | ✔ | 99% | |||||||||||||||||
| Pentoxyverine citrate | ✔ | 98% | |||||||||||||||||
| Solifenacin | ✔ | 98% | |||||||||||||||||
| Catharanthine | ✔ | 98% | |||||||||||||||||
| Benzethonium chloride | +++ α4β2 nAChRs, IC50: 49 nM α7 nAChRs, IC50: 122 nM | 99+% | |||||||||||||||||
| Vinblastine sulfate | + nAChR, IC50: 8.9 μM | 99% | |||||||||||||||||
| PNU-120596 | ++ α7 nAChR, EC50: 216 nM | 99+% | |||||||||||||||||
| 1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 | |||||||||||||||||||
| 靶点 | 
 | 
| 描述 | Cisatracurium Besylate is an ideal non-depolarizing muscle relaxant. The inhibitory effect of cisatracurium besylate on the proliferation activity of endothelial cells was time-dependent. Cisatracurium Besylate (0, 5, 25, or 100 µM) make the number of the autolysomes increases in a concentration dependent manner. Moreover, cisatracurium besylate can injure cells through autophagic cell death[3]. Cisatracurium besylate is frequently used in the intensive care unit in order to induce muscle relaxation to facilitate mechanical ventilation in critically ill patients[4]. | 
| Concentration | Treated Time | Description | References | |
| mouse MLTC-1 tumor cells | 5, 10, 50 μmol/L | 12 h | Cisatracurium significantly increased testosterone output in mouse MLTC-1 cells | J Cell Mol Med. 2020 Dec;24(24):14184-14194 | 
| rat adult Leydig cells | 5, 10, 50 μmol/L | 12 h | Cisatracurium significantly increased testosterone output in rat Leydig cells | J Cell Mol Med. 2020 Dec;24(24):14184-14194 | 
| Human microvascular endothelial cells (HMECs) | 0.32, 0.64, and 1.28 μM | 24 h | To investigate the effect of cisatracurium on LPS-induced MMP3 expression. Results showed that cisatracurium significantly decreased LPS-induced MMP3 expression and increased the expression of junctional proteins such as VE-cadherin and claudin-5. | Biosci Trends. 2021 Mar 15;15(1):50-54 | 
| NCT号 | 适应症或疾病 | 临床期 | 招募状态 | 预计完成时间 | 地点 | 
| NCT01181349 | - | Completed | - | - | |
| NCT02793323 | Relieve Shoulder Pain After La... 展开 >>paroscopic Surgeries 收起 << | Not Applicable | Completed | - | Lebanon ... 展开 >> Makassed General Hospital Beirut, Lebanon 收起 << | 
| NCT02154074 | Perioperative Blood Glucose an... 展开 >>d Insulin 收起 << | Phase 4 | Unknown | October 2014 | China, Shanxi ... 展开 >> SecondXianJiaotongU Recruiting Xi'an, Shanxi, China Contact: Hongtao Liu 13572225310 lannylouis@163.com 收起 << | 
| 计算器 | ||||
| 存储液制备 |  | 1mg | 5mg | 10mg | 
| 1 mM 5 mM 10 mM | 0.80mL 0.16mL 0.08mL | 4.02mL 0.80mL 0.40mL | 8.04mL 1.61mL 0.80mL | |
| CAS号 | 96946-42-8 | 
| 分子式 | C65H82N2O18S2 | 
| 分子量 | 1243.48 | 
| SMILES Code | O=C(OCCCCCOC(CC[N@+]1(C)[C@H](CC2=CC=C(OC)C(OC)=C2)C3=C(C=C(OC)C(OC)=C3)CC1)=O)CC[N@+]4(C)[C@H](CC5=CC=C(OC)C(OC)=C5)C6=C(C=C(OC)C(OC)=C6)CC4.O=S(C7=CC=CC=C7)([O-])=O.O=S(C8=CC=CC=C8)([O-])=O | 
| MDL No. | MFCD00871018 | 
| 别名 | 顺苯磺酸阿曲库铵 ;51W89 besylate; Cisatracurium besilate; Cisatracurium (besylate); 51W89 | 
| 运输 | 蓝冰 | 
| InChI Key | XXZSQOVSEBAPGS-DONVQRBFSA-L | 
| Pubchem ID | 62886 | 
| 存储条件 | In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, store in freezer, under -20°C | 
| 溶解方案 | H2O: 50 mg/mL(40.21 mM) 
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