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Ropivacaine

Cat. No. M10492

All AbMole products are for research use only, cannot be used for human consumption.

Ropivacaine Structure
Synonym:

Narop; Noropine; LEA-103

Size Price Availability Quantity
5mg USD 30  USD30 In stock
10mg USD 45  USD45 In stock
50mg USD 80  USD80 In stock
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Quality Control & Documentation
Biological Activity

Ropivacaine is a member of the amino amide class of local anesthetics and acts as a potent sodium channel blocker. 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. Ropivacaine prevents pressure-induced lung edema and associated hyperpermeability as evidence by maintaining PaO2, lung wet-to-dry ratio and plasma volume in levels similar to sham rats.

Chemical Information
Molecular Weight 274.40
Formula C17H26N2O
CAS Number 84057-95-4
Solubility (25°C) DMSO 10 mg/mL
Water 10 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Milan Patel, et al. Life Sci. Ropivacaine inhibits pressure-induced lung endothelial hyperpermeability in models of acute hypertension

[2] Teng-Fei Li, et al. PLoS One. Epidural sustained release ropivacaine prolongs anti-allodynia and anti-hyperalgesia in developing and established neuropathic pain

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

[4] Dene Simpson, et al. Drugs. Ropivacaine: a review of its use in regional anaesthesia and acute pain management

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Keywords: Ropivacaine, Narop; Noropine; LEA-103 supplier, Animal experimental anesthetics, inhibitors, activators

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