Ropivacaine
Ropivacain is a potent sodium channel blocker. Ropivacain 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 used for the research of neuropathic pain management[1].
Product Specifications
CAS Number
[84057-95-4]
UNSPSC
12352005
Hazard Statement
H302
Target
Potassium Channel; Sodium Channel
Type
Reference compound
Related Pathways
Membrane Transporter/Ion Channel
Applications
Neuroscience-Neuromodulation
Field of Research
Neurological Disease; Cardiovascular Disease; Cancer
Assay Protocol
https://www.medchemexpress.com/ropivacaine.html
Purity
99.98
Solubility
DMSO : 12.5 mg/mL (ultrasonic)
Smiles
O=C([C@H]1N(CCC)CCCC1)NC2=C(C)C=CC=C2C
Molecular Formula
C17H26N2O
Molecular Weight
274.40
Precautions
H302
References & Citations
Shipping Conditions
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Scientific Category
Reference compound1
Clinical Information
Launched
Citation 01
Available Sizes
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