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Bioorg Med Chem Lett ; 24(24): 5695-5698, 2014 Dec 15.
Article in English | MEDLINE | ID: mdl-25467164

ABSTRACT

Serotonin was linked by amidation to the carboxylic acid groups of a series of structurally diverse NSAIDs. The resulting NSAID-serotonin conjugates were tested in vitro for their ability to inhibit FAAH, TRPV1, and COX2. Ibuprofen-5-HT and Flurbiprofen-5-HT inhibited all three targets with approximately the same potency as N-arachidonoyl serotonin (AA-5-HT), while Fenoprofen-5-HT and Naproxen-5-HT showed activity as dual inhibitors of TRPV1 and COX2.


Subject(s)
Amidohydrolases/antagonists & inhibitors , Anti-Inflammatory Agents, Non-Steroidal/chemistry , Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Cyclooxygenase 2/chemistry , Serotonin/chemistry , TRPV Cation Channels/antagonists & inhibitors , Flurbiprofen/chemistry , Flurbiprofen/metabolism , Humans , Serotonin/metabolism
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