生物活性 | |||
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描述 | Ropivacaine hydrochloride monohydrate acts as a potent sodium channel blocker, inhibiting impulse conduction through reversible suppression of sodium ion influx in nerve fibers[1].[2]. Ropivacaine also functions as an inhibitor of the K2P (two-pore domain potassium channel) TREK-1, demonstrating an IC50 of 402.7 μM in the membranes of COS-7 cells[3]. Ropivacaine is commonly utilized in vivo for regional anesthesia and managing neuropathic pain[1]. |
临床研究 | |||||
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NCT号 | 适应症或疾病 | 临床期 | 招募状态 | 预计完成时间 | 地点 |
NCT02527577 | Liver Cancer, Adult | Not Applicable | Terminated(difficulties to rec... 展开 >>ruit patients) 收起 << | - | France ... 展开 >> CHU de SAINT-ETIENNE Saint-etienne, France, 42000 收起 << |
NCT02438852 | Bladder Carcinoma ... 展开 >> Post-operative Pain 收起 << | Phase 3 | Not yet recruiting | February 25, 2022 | United States, California ... 展开 >> USC / Norris Comprehensive Cancer Center Not yet recruiting Los Angeles, California, United States, 90033 Contact: Ileana Aldana 323-865-3700 Ileana.aldana@med.usc.edu Principal Investigator: Siamak Daneshmand, MD Sub-Investigator: Brian Hu, MD 收起 << |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
3.04mL 0.61mL 0.30mL |
15.20mL 3.04mL 1.52mL |
30.41mL 6.08mL 3.04mL |
参考文献 |
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