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Ropivacaine HCl monohydrate

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Chemical Structure| 132112-35-7 同义名 : 盐酸罗哌卡因 ;(–)-Ropivacaine (hydrochloride hydrate);LEA 103;(S)-Ropivacaine;Ropivacaine hydrochloride monohydrate
CAS号 : 132112-35-7
货号 : A671024
分子式 : C17H29ClN2O2
纯度 : 99+%
分子量 : 328.877
MDL号 : MFCD00946578
存储条件:

粉末 Inert atmosphere,2-8°C

液体 -20°C:3-6个月-80°C:12个月

溶解度 :

DMSO: 105 mg/mL(319.27 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

H2O: 50 mg/mL(152.03 mM),配合低频超声助溶

动物实验配方:
生物活性
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
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
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

[1]Dene Simpson, et al. Ropivacaine: a review of its use in regional anaesthesia and acute pain management. Drugs. 2005;65(18):2675-717.

[2]Li TF, et al. Epidural sustained release ropivacaine prolongs anti-allodynia and anti-hyperalgesia in developing and established neuropathic pain. PLoS One. 2015 Jan 24;10(1):e0117321.

[3]Hye Won Shin, et al. The inhibitory effects of bupivacaine, levobupivacaine, and ropivacaine on K2P (two-pore domain potassium) channel TREK-1. J Anesth. 2014 Feb;28(1):81-6.