- QX 314 chloride
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- $1.10 / 1g
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2022-05-13
- CAS:5369-03-9
- Min. Order: 1g
- Purity: 99.0% Min
- Supply Ability: 100 Tons
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| 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 | EINECS: | | 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) |
| 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 |
| QX 314 chloride Preparation Products And Raw materials |
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