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Benzamil

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Catalog No. T5850Cas No. 2898-76-2

Benzamil is an epithelial sodium channel (ENaC) blocker that inhibits sodium transport from (IC50 = 4 nM) and binds to (Kd = 5 nM) bovine kidney cortex membrane vesicles.

Benzamil

Benzamil

🥰Excellent
Purity: 99.79%
Catalog No. T5850Cas No. 2898-76-2
Benzamil is an epithelial sodium channel (ENaC) blocker that inhibits sodium transport from (IC50 = 4 nM) and binds to (Kd = 5 nM) bovine kidney cortex membrane vesicles.
Pack SizePriceAvailabilityQuantity
5 mg$50In Stock
10 mg$60In Stock
25 mg$126In Stock
50 mg$239In Stock
100 mg$432In Stock
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Purity:99.79%
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Product Introduction

Bioactivity
Description
Benzamil is an epithelial sodium channel (ENaC) blocker that inhibits sodium transport from (IC50 = 4 nM) and binds to (Kd = 5 nM) bovine kidney cortex membrane vesicles.
In vivo
nd also examined the role of ASICs on modulation of neuropathic pain.?Neuropathic pain was induced by L4-5 spinal nerve ligation in male Sprague-Dawley rats weighing 100-120 g, and intrathecal catheterization was performed for drug administration.?The effects of amiloride and benzamil were measured by the paw-withdrawal threshold to a mechanical stimulus using the up and down method.?The expression of ASICs in the spinal cord dorsal horn was also analyzed by RT-PCR.?Intrathecal amiloride and benzamil significantly increased the paw withdrawal threshold in spinal nerve-ligated rats (87%±12% and 76%±14%, P=0.007 and 0.012 vs vehicle, respectively).?Spinal nerve ligation increased the expression of ASIC3 in the spinal cord dorsal horn (P=0.01), and this increase was inhibited by both amiloride and benzamil (P<0.001 in both).?Intrathecal amiloride and benzamil display antinociceptive effects in the rat spinal nerve ligation model[1].
Animal Research
On the day of the experiment, rats were allocated into experimental and control groups for the tested drugs.?Control groups were performed using intrathecal DMSO (n=5) or methanol (n=5) according to the solvent used for the tested drugs.?All experiments were performed by investigators blinded to the treatment.?To assess the effects of both drugs, increasing doses of amiloride (1, 3, 10 μg in 10 μL, n=5-7) or benzamil (3, 10, 30 μg in 10 μL, n=5-7) were investigated.?The withdrawal threshold was measured prior to spinal nerve ligation and was regarded as pre-ligated threshold.?The withdrawal threshold was measured immediately prior to intrathecal drug delivery and was regarded as a post-ligated baseline threshold.?The withdrawal threshold was determined at 15, 30, 60, 90, 120, 150, and 180 min following intrathecal administration of the experimental drugs.For the purpose of examining the behavioral changes by amiloride and benzamil, the highest dose of each drug was administered intrathecally to 10 additional rats.?Motor function was assessed by the righting reflex and placing-stepping reflex[1].
Chemical Properties
Molecular Weight319.75
FormulaC13H14ClN7O
Cas No.2898-76-2
SmilesC(NC(NCC1=CC=CC=C1)=N)(=O)C=2C(N)=NC(N)=C(Cl)N2
Relative Density.1.59 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 3.2 mg/mL (10 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.1274 mL15.6372 mL31.2744 mL156.3722 mL
5 mM0.6255 mL3.1274 mL6.2549 mL31.2744 mL
10 mM0.3127 mL1.5637 mL3.1274 mL15.6372 mL

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