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Lidocaine N-ethyl chloride

Cat. No. M7884
Lidocaine N-ethyl chloride Structure
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Biological Activity

Lidocaine N-ethyl chloride is an intracellular voltage-gated sodium channel blocker.

Chemical Information
Molecular Weight 298.85
Formula C16H27N2OCl
CAS Number 5369-03-9
Solubility (25°C) Water: soluble
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] W Kilb, et al. Characterization of a hyperpolarization-activated inward current in Cajal-Retzius cells in rat neonatal neocortex

[2] K Harsanyi, et al. Transient synaptic potentiation in the visual cortex. I. Cellular mechanisms

[3] P S Mangan, et al. Profound disturbances of pre- and postsynaptic GABAB-receptor-mediated processes in region CA1 in a chronic model of temporal lobe epilepsy

[4] A N Katchman, et al. Mechanism of early anoxia-induced suppression of the GABAA-mediated inhibitory postsynaptic current

[5] J Vautrin, et al. Fast presynaptic GABAA receptor-mediated Cl- conductance in cultured rat hippocampal neurones

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