Inhibition of FAAH, TRPV1, and COX2 by NSAID–serotonin conjugates

Inhibition of FAAH, TRPV1, and COX2 by NSAID–serotonin conjugates N-Caffeoyl serotonin as selective COX-2 inhibitor 1-Heteroarylpropan-2-ones as inhibitors of fatty acid amide hydrolase: Studies on structure-activity relationships and metabolic stability Synthesis and Evaluation of Paracetamol Esters As Novel Fatty Acid Amide Hydrolase Inhibitors Further exploration of the structure-activity relationship of dual soluble epoxide hydrolase/fatty acid amide hydrolase inhibitors Mining biologically-active molecules for inhibitors of fatty acid amide hydrolase (FAAH): Identification of phenmedipham and amperozide as FAAH inhibitors New FAAH inhibitors based on 3-carboxamido-5-aryl-isoxazole scaffold that protect against experimental colitis Paracetamol analogues conjugated by FAAH induce TRPV1-mediated antinociception without causing acute liver toxicity Novel inhibitors of fatty acid amide hydrolase Design, synthesis and evaluation of novel indomethacin–flavonoid mutual prodrugs as safer NSAIDs