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QX-314 bromide

🥰Excellent
Catalog No. T16707Cas No. 24003-58-5

QX-314 bromide is a membrane-impermeable sodium channel blocker that inhibits TRPV1 and NaV1.8 expression, causing sensory-selective blockade of TRPV1 channels. It exhibits anti-inflammatory effects and may be used in studies of gastroesophageal reflux disease (GERD).

QX-314 bromide

QX-314 bromide

🥰Excellent
Purity: 99.05%
Catalog No. T16707Cas No. 24003-58-5
QX-314 bromide is a membrane-impermeable sodium channel blocker that inhibits TRPV1 and NaV1.8 expression, causing sensory-selective blockade of TRPV1 channels. It exhibits anti-inflammatory effects and may be used in studies of gastroesophageal reflux disease (GERD).
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$39-In Stock
5 mg$90-In Stock
10 mg$129-In Stock
25 mg$219-In Stock
50 mg$323-In Stock
100 mg$483-In Stock
1 mL x 10 mM (in DMSO)$97-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.05%
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Product Introduction

Bioactivity
Description
QX-314 bromide is a membrane-impermeable sodium channel blocker that inhibits TRPV1 and NaV1.8 expression, causing sensory-selective blockade of TRPV1 channels. It exhibits anti-inflammatory effects and may be used in studies of gastroesophageal reflux disease (GERD).
In vitro
QX-314 bromide (1-60 mM) can directly activate TRPV1 channels in a concentration-dependent manner [1].
QX-314 bromide (≥30 mM) causes darkening of the oocyte membrane and induces cell death [1].
In vivo
QX-314 bromide (0.2%, 10 μl, 1.6 mg/kg, plantar injection) combined with 1% lidocaine significantly prolonged the response latency to thermal and mechanical stimuli in rats [2].
QX-314 bromide (0.2%, intradermal injection) combined with 1% lidocaine completely suppressed the cutaneous trunci muscle reflex (CTMR) evoked by needle stimulation in rats, with a blockade duration of up to 6 hours [2].
QX-314 bromide (0.2%, perisciatic injection) combined with varying concentrations of lidocaine (0.5%-2%) produced dose-dependent long-lasting nociceptive blockade [2].
Chemical Properties
Molecular Weight343.3
FormulaC16H27BrN2O
Cas No.24003-58-5
Smiles[Br-].O=C(NC=1C(=CC=CC1C)C)C[N+](CC)(CC)CC
Relative Density.no data available
ColorWhite
AppearanceSolid
Storage & Solubility Information
Storagekeep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 40 mg/mL (116.52 mM), Sonication is recommended.
H2O: 80 mg/mL (233.03 mM), Sonication is recommended.
Solution Preparation Table
DMSO/H2O
1mg5mg10mg50mg
1 mM2.9129 mL14.5645 mL29.1290 mL145.6452 mL
5 mM0.5826 mL2.9129 mL5.8258 mL29.1290 mL
10 mM0.2913 mL1.4565 mL2.9129 mL14.5645 mL
20 mM0.1456 mL0.7282 mL1.4565 mL7.2823 mL
50 mM0.0583 mL0.2913 mL0.5826 mL2.9129 mL
100 mM0.0291 mL0.1456 mL0.2913 mL1.4565 mL

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TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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