QX 314 chloride
QX 314 chloride Basic information
- Product Name:
- QX 314 chloride
- Synonyms:
-
- QX 314 CHLORIDE
- N-(2,6-DIMETHYLPHENYLCARBAMOYLMETHYL)TRIETHYLAMMONIUM CHLORIDE
- QX314.Cl
- 2-(2,6-Dimethylphenylamino)-N,N,N-triethyl-2-oxoethanaminium chloride
- [2-(2,6-dimethylanilino)-2-keto-ethyl]-triethyl-ammonium chloride
- [2-(2,6-dimethylanilino)-2-oxoethyl]-triethylazanium chloride
- [2-[(2,6-dimethylphenyl)amino]-2-oxo-ethyl]-triethyl-azanium chloride
- Lidocaine N-ethyl chloride
- CAS:
- 5369-03-9
- MF:
- C16H27ClN2O
- MW:
- 298.85
- Product Categories:
-
- Ion Channels
- Mol File:
- 5369-03-9.mol
QX 314 chloride Chemical Properties
- Melting point:
- 209-211 °C
- storage temp.
- Room temp
- solubility
- insoluble in EtOH; ≥14.95 mg/mL in DMSO with gentle warming; ≥22.3 mg/mL in H2O
- form
- solid
- color
- White
- Water Solubility
- Soluble in water (100mM)
Safety Information
- Safety Statements
- 22-24/25
- WGK Germany
- 3
MSDS
- Language:English Provider:SigmaAldrich
QX 314 chloride Usage And Synthesis
Uses
QX 314 Chloride has been shown to have antitussive properties in mammalian animal models.
Uses
QX 314 chloride is a membrane-impermeant lidocaine derivative that selectively blocks sodium channels on nociceptive neurons when delivered intracellularly via the TRPV1 channel, but is reportedly ineffective with extracellular application. When supplied in combination with 1 μM capsaicin , a TRPV1 receptor agonist, 5 mM QX-314 blocks 98% of sodium current in voltage-clamped nociceptive DRG neurons. QX 314 chloride elicits a long-lasting decrease in the response to painful mechanical and thermal stimuli without imparting the motor deficits (e.g., numbness, paralysis) associated with many conventional local anesthetics. At concentrations ranging from 10-70 mM, peripheral application of QX 314 chloride dose-dependently produces robust local anesthesia with slow onset in the guinea pig intradermal wheal assay, the mouse tail-flick test, and the mouse sciatic nerve blockade model.
Biological Activity
Membrane impermeable quaternary derivative of lidocaine, a blocker of voltage-activated Na + channels.
Biochem/physiol Actions
Lidocaine N-ethyl chloride is an intracellular voltage-gated sodium channel blocker.
storage
Room temperature
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