• Skip to primary navigation
  • Skip to main content
  • Skip to footer

LKT Labs

Biochemicals for Life Science Research

  • Products
    • New Products
    • Cancer Biology
    • Cardiovascular
    • Endocrine Signaling and Immunology
    • Metabolic and GI Pathology
    • Microbiology
    • Natural Products
    • Neuroscience
    • Peptides
    • Pharmaceutical Impurities and Derivatives
    • Stem Cell Modulators
  • Services
    • Custom Synthesis
    • Natural Product Isolation
    • Analytical Services
  • Int’l Distributors
  • Support
    • About LKT Labs
    • General Inquiry
    • Bulk Quote Request
    • Document Request
    • Technical Support
    • Catalog Request
    • Product Flyers
  • Contact Us
  • Cart
  • Login / Register
URB597

URB597

Product ID U682040
Cas No. 546141-08-6
Purity ≥98%
Product Unit SizeCostQuantityStock
5 mg $57.20 In stock
25 mg $193.30 In stock
100 mg $565.10 In stock
Bulk Quote

Quicklinks

  • Description
  • Product Info
  • Shipping and Storage
  • Downloads
  • References
  • Description
  • Product Info
  • Shipping and Storage
  • Downloads
  • References
  • Custom Order

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

Custom Order

  • Size of single unit expressed as number (e.g. '500' in the case of 500 mg)
  • Total quantity of unit size desired (e.g. '10' in the case of 10 x 500 mg). If only one unit is desired, you may leave this blank.
  • This field is for validation purposes and should be left unchanged.

Related Products

  • O5212

    Ondansetron Hydrochloride Dihydrate

    5-HT3 antagonist.

    ≥98%
  • A225822

    Afuresertib

    Inhibitor of Akt.

    ≥98%
  • T6902

    Tranilast

    Mast cell stabilizer; TRPV2 antagonist, PDGFR i...

    ≥98%
  • E6231

    (−)-Epicatechin

    Flavanol originally found in Camilla (green tea...

    ≥93%
  • A5276

    Angiotensin I, human

    Endogenous peptide, cleavage product of angiote...

    ≥98%
  • C0006

    Cabozantinib

    VEGFR2, c-Met, RET inhibitor.

    ≥98%
  • O4104

    Okadaic Acid Sodium

    Shellfish toxin produced by dinoflagellates and se...
    ≥98%
  • E9416

    Exendin-3

    Peptide, GLP-1 analog found in Heloderma; GLP-1...

    ≥95%
  • T0119

    Taxol Side Chain β-lactam

    Taxol synthesis intermediate.

    ≥98%
  • C022692

    Carbinoxamine Maleate

    Histamine H1-antagonist

    ≥98%
  • H9716

    (E,Z)-4-Hydroxytamoxifen

    Selective estrogen receptor modulator.

    ≥97%
  • R1876

    all-trans-Retinol

    Diterpene component of vitamin A, differentiation ...
    ≥95%
  • V3345

    Vildagliptin

    DPP4 inhibitor.

    ≥98%
  • M3368

    Mirtazapine

    Piperazine; 5-HT1 agonist, 5-HT2/3 and α2-adre...

    ≥98%
  • M9356

    Myomodulin

    Proton pump inhibitor

    ≥95%
  • D3201

    Diallyl Sulfide

    Organosulfur found in garlic.

    ≥98%
  • C8070

    Curcumin, high purity

    Active compound found in turmeric; MST1 activat...

    ≥98%
  • E5569

    Enramycin B

    Polypeptide; peptidoglycan inhibitor.

    ≥83%
  • J0274

    Jasplakinolide

    Marine toxin; actin polymerization inducer.

    ≥98%
  • O451328

    Oligomycin C

    Macrocyclic lactone.

    ≥97%

Footer

  • Contact Us
  • About Us
  • Site Map
  • Terms and Conditions
LKT Laboratories, Inc.
545 Phalen Blvd.
St. Paul MN, 55130

Ph: (888)-558-5227
Fax: (888)-558-7329

©2025 LKT Laboratories, All Rights Reserved - Products for research use only