Share this post on:

product name Nefopam HCl


Description: Nefopam HCl is a centrally-acting but non-opioid analgesic drug by blocking voltage-gated sodium channel and inhibition of serotonin, dopamine and noradrenaline reuptake. The mechanism of analgesia is not completely understood, it appears that nefopam is a centrally acting, non-opioid analgesic that inhibits reuptake of serotonin, norepinephrine, and dopamine.

References: Br J Anaesth. 2008 Nov;101(5):610-7. 



Molecular Weight (MW)

289.8 
Formula

C17H19NO.HCl 
CAS No.

23327-57-3 
Storage

-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)

DMSO: <1 mg/mL 
Water: 21 mg/mL (72.5 mM)
Ethanol: <1 mg/mL
Solubility (In vivo)

 
Synonyms

 

other peoduct :

In Vitro

In vitro activity: The mechanism of analgesia is not completely understood, it appears that nefopam is a centrally acting, non-opioid analgesic that inhibits reuptake of serotonin, norepinephrine, and dopamine.


Kinase Assay:


Cell Assay

In Vivo Using the tail-flick and hot-plate assays, nefopam is tested for analgesic activity following intraperitoneal (i.p.), intracranial (i.c.) and intraspinal (i.s.) injection in mice. Nefopam is one-third as potent as morphine on the hot-plate test, but does not affect the tail-flick. 
Animal model  
Formulation & Dosage  
References Br J Anaesth. 2008 Nov;101(5):610-7.  

Ebselen

Share this post on:

Author: Sodium channel