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Ropivacaine (hydrochloride)
SKU
HY-B0563B-10 mg
Category Reference compound
Tags Membrane Transporter/Ion Channel, Neurological Disease; Cardiovascular Disease; Cancer, Potassium Channel;Sodium Channel
$32 – $79
Products Details
Product Description
– Ropivacaine hydrochloride is a potent sodium channel blocker and blocks impulse conduction via reversible inhibition of sodium ion influx in nerve fibrese[1][2]. Ropivacaine is also an inhibitor of K2P (two-pore domain potassium channel) TREK-1 with an IC50 of 402.7 μM in COS-7 cell’s membrane[3]. Ropivacaine is widely used for neuropathic pain management in vivo[1].
Web ID
– HY-B0563B
Storage Temperature
– 4°C (Powder, sealed storage, away from moisture)
Shipping
– Room Temperature
Applications
– Neuroscience-Neuromodulation
Molecular Formula
– C17H27ClN2O
Citations
– Eur Spine J. 2022 Sep 24.|Stem Cell Res Ther. 2021 Feb 4;12(1):107.|J Toxicol Sci. 2023;48(3):139-148.
References
– [1]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.|[2]Dene Simpson, et al. Ropivacaine: a review of its use in regional anaesthesia and acute pain management. Drugs. 2005;65(18):2675-717.|[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.|[4]Milan Patel, et al. Ropivacaine Inhibits Pressure-Induced Lung Endothelial Hyperpermeability in Models of Acute Hypertension. Life Sci. 2019 Apr 1;222:22-28.
CAS Number
– 98717-15-8
Molecular Weight
– 310.86
Compound Purity
– 99.93
SMILES
– [H]Cl.O=C([C@H]1N(CCC)CCCC1)NC2=C(C)C=CC=C2C
Clinical Information
– Launched
Research Area
– Neurological Disease; Cardiovascular Disease; Cancer
Solubility
– DMSO : 10 mg/mL (ultrasonic)|H2O : 10 mg/mL (ultrasonic)
Target
– Potassium Channel;Sodium Channel
Pathway
– Membrane Transporter/Ion Channel
Product type
– Reference compound
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