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Ropivacaine mesylate

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Ropivacaine mesylate Basic information

Product Name:
Ropivacaine mesylate
Synonyms:
  • ROPIVACAINE MESYLATE
  • (2S)-N-(2,6-Dimethylphenyl)-1-propyl-2-piperidinecarboxamide monomethanesulfonate
  • Ropivacaine Mesylate API
  • Ropivacaine mesylate (2S)-N-(2,6-Dimethylphenyl)-1-propyl-2-piperidinecarboxamide monomethanesulfonate
  • Ropivacaine Mesylate Injection
  • Ropivacaine mesylate USP/EP/BP
  • (S)-N-(2,6-Dimethylphenyl)-1-propylpiperidine-2-carboxamidemethanesulfonate
  • TIANFUCHEM--854056-07-8--Ropivacaine mesylate in stock
CAS:
854056-07-8
MF:
C18H30N2O4S
MW:
370.51
EINECS:
264-407-7
Product Categories:
  • 854056-07-8
Mol File:
854056-07-8.mol
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Ropivacaine mesylate Chemical Properties

storage temp. 
Store at -20°C
form 
Solid
color 
White to off-white
Water Solubility 
Water: 250 mg/mL (674.75 mM)
InChI
InChI=1/C17H26N2O.CH4O3S/c1-4-11-19-12-6-5-10-15(19)17(20)18-16-13(2)8-7-9-14(16)3;1-5(2,3)4/h7-9,15H,4-6,10-12H2,1-3H3,(H,18,20);1H3,(H,2,3,4)/t15-;/s3
InChIKey
YPTSIOMXZOPKAF-AVAJOTNLNA-N
SMILES
S(O)(=O)(=O)C.C([C@@H]1CCCCN1CCC)(=O)NC1C(=CC=CC=1C)C |&1:6,r|
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Ropivacaine mesylate Usage And Synthesis

Uses

Ropivacaine mesylate is a long-acting amide local anaesthetic agent for a spinal block and effectively blocks neuropathic pain. Ropivacaine blocks impulse conduction via reversible inhibition of?sodium ion influx?in nerve fibressup>[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].

in vivo

Epidural administration of Ropivacaine mesylate effectively blocks neuropathic pain (both mechanical allodynia and heat hyperalgesia) without induction of analgesic tolerance and significantly delays the development of neuropathic pain produced by peripheral nerve injury[1].
Ropivacaine mesylate inhibits pressure-induced increases in filtration coefficient (Kf) without affecting pulmonary artery pressure (Ppa), pulmonary capillary pressures (Ppc), and zonal characteristics (ZC)[2].
Ropivacaine mesylate 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[2].
Ropivacaine mesylate inhibits pressure-induced NO production as evidenced by decreased lung nitro-tyrosine content when compared to hypertensive lungs[2].

Animal Model:Adult Sprague-Dawley rats (300-400g)[2]
Dosage:1 μM
Administration:Infusion (added to the perfusate reservoir)
Result:Attenuated pressure-dependent increases in filtration coefficient (Kf).

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. DOI:10.1371/journal.pone.0117321
[2] Milan Patel, et al. Ropivacaine Inhibits Pressure-Induced Lung Endothelial Hyperpermeability in Models of Acute Hypertension. Life Sci. 2019 Apr 1;222:22-28. DOI:10.1016/j.lfs.2019.02.053
[3] Dene Simpson, et al. Ropivacaine: a review of its use in regional anaesthesia and acute pain management. Drugs. 2005;65(18):2675-717. DOI:10.2165/00003495-200565180-00013
[4] 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. DOI:10.1007/s00540-013-1661-1

Ropivacaine mesylateSupplier

Anhui Wellman Pharmaceutical Co., Ltd. Gold
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0551-65322016
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welman@welman.com
Shanghai Boyle Chemical Co., Ltd.
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JinYan Chemicals(ShangHai) Co.,Ltd.
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13817811078
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Jia Xing Isenchem Co.,Ltd
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0573-85285100 18627885956
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Shanghai Hanhong Scientific Co.,Ltd.
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021-54306202 13764082696
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info@hanhongsci.com
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