Skip to main content

Table 3 Potencies of NSAIDs as inhibitors of rat liver oleamide hydrolase activity

From: Assessment of NSAIDs as potential inhibitors of the fatty acid amide hydrolase I (FAAH-1) using three different primary fatty acid amide substrates in vitro

NSAID

pIC50 (M)

NSAID

pIC50 (M)

Sulindac

3.65 ± 0.08

Ibuprofen

3.01 ± 0.06

Carprofen

3.58 ± 0.09

Valdecoxib

3.00 ± 0.15

Meclofenamic acid

3.57 ± 0.06

Ketorolac

2.91 ± 0.07

Sulindac sulphone

3.35 ± 0.03

Diclofenac

2.90 ± 0.07

Indomethacin

3.28 ± 0.03

Dipyrone

2.77 ± 0.07

Diflunisal

3.15 ± 0.04

  
  1. Data are mean ± SEM (Standard Error of the Mean) of four separate preparations (n=4) conducted in triplicate