LKT Labs

Biochemicals for Life Science Research

URB597

Product ID U682040
Cas No. 546141-08-6
Purity ≥98%
Product Unit SizeCostQuantityStock
5 mg $47.60 In stock
25 mg $160.80 In stock
100 mg $470.30 In stock
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Description

URB597 is an inhibitor of fatty acid amide hydrolase (FAAH). FAAH inhibition leads to an increase of anandamide, a naturally occurring substrate for the cannabinoid receptors. Increase in anandamide and activation of the CB receptors decreases sensitivity to pain in rat models. Additionally, URB597 also decreases the amount of tyrosine hydrolase in neurons in a CB receptor/FAAH independent manner. URB597 also demonstrates an anti-neuroinflammatory effect in Sprague-Dawley rat models. URB597 shows analgesic effects in numerous pain models

Product Info

Cas No.

546141-08-6
Purity

≥98%
Formula

C20H22N2O3
Formula Wt.

338.41
Chemical Name

Cyclohexylcarbamic acid 3´-carbamoyl-biphenyl-3-yl ester
IUPAC Name

[3-(3-carbamoylphenyl)phenyl] N-cyclohexylcarbamate
Solubility

50mM in DMSO
Appearance

White powder

Shipping and Storage

Store Temp

-20°C
Ship Temp

Ambient

Downloads

MSDS

U682040 MSDS PDF
Info Sheet

U682040 Info Sheet PDF

References

Murphy N, Cowley TR, Blau CW et al. The fatty acid amide hydrolase inhibitor URB597 exerts anti-inflammatory effects in hippocampus of aged rats and restores an age-related deficit in long-term potentiation. J Neuroinflammation. 2012 Apr 26;9:79. PMID: 22537429.

Bosier B, Muccioli GG, and Lamber DM. The FAAH inhibitor URB597 efficiently reduces tyrosine hydroxylase expression through CB1 and FAAH-independent mechanisms. Br J Pharmacol. 2013 Jun;169(4):794-807. PMID: 22970888

Kwilasz AJ, Abdullah RA, Poklis JL et al. Effects of the fatty acid amide hydrolase inhibitor URB597 on pain-stimulated and pain-depressed behavior in rats. Behav Pharmacol. 2014 Apr;25(2):119-29. PMID: 24583930

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