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QX-314 bromide£¬IC-0356953
Click£º5675     Release date£º2019-3-7    Author£ºAdministrator    Source£ºOriginal

QX-314 bromide ,24003-58-5

Cat.No.:IC-0356953

Product Information

Biological Activity

QX-314 bromide is a membrane-impermeable permanently charged sodium channel blocker.

Conversion of different model animals based on BSA (Value based on data from FDA Draft Guidelines)

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 resveratrol used for a mouse (22.4 mg/kg) to a dose based on the BSA for a rat, multiply 22.4 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 resveratrol of 11.2 mg/kg.

Order Information

 

Quantity

Price($)

Price(€)

Price(£¤/CNY)

10mg

$53.00

€63.60

£¤530.00

50mg

$211.00

€253.20

£¤2,110.00

100mg

$378.00

€453.60

£¤3,780.00

Free Delivery on orders over $350.00.

Chemical Information

Molecular Weight

343.3

Formula

C16H27BrN2O

CAS Number

24003-58-5

Purity

>98.00%

Solubility

H2O : 100 mg/mL (291.29 mM)

Storage

4¡ãC, protect from light

Reference

[1]. Rivera-Acevedo RE, et al. The quaternary lidocaine derivative, QX-314, exerts biphasic effects on transient receptor potential vanilloid subtype 1 channels in vitro. Anesthesiology. 2011 Jun;114(6):1425-34.
[2]. Binshtok AM, et al. Coapplication of lidocaine and the permanently charged sodium channel blocker QX-314 produces a long-lasting nociceptive blockade in rodents. Anesthesiology. 2009 Jul;111(1):127-37.
[3]. Talbot MJ, et al. Intracellular QX-314 inhibits calcium currents in hippocampal CA1 pyramidal neurons. J Neurophysiol. 1996 Sep;76(3):2120-4.

We Devoted Ourselves To The Development Of Biomedical Research Reagent.

On an article£ºNRF2 Inhibitor,IC-0199622
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