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Bioorg Med Chem Lett ; 8(20): 2839-44, 1998 Oct 20.
Article in English | MEDLINE | ID: mdl-9873633

ABSTRACT

In search of antiinflammatory drugs with a new mechanism of action, U0126 was found to functionally antagonize AP-1 transcriptional activity via noncompetitive inhibition of the dual specificity kinase MEK with an IC50 of 0.07 microM for MEK 1 and 0.06 microM for MEK 2. U0126 can undergo isomerization and cyclization reactions to form a variety of products, both chemically and in vivo, all of which exhibit less affinity for MEK and lower inhibition of AP-1 activity than parent, U0126.


Subject(s)
Butadienes/chemistry , Enzyme Inhibitors/chemistry , Nitriles/chemistry , Protein Serine-Threonine Kinases/antagonists & inhibitors , Animals , Anti-Inflammatory Agents/chemistry , Anti-Inflammatory Agents/pharmacokinetics , Anti-Inflammatory Agents/pharmacology , Biotransformation , Butadienes/pharmacokinetics , Butadienes/pharmacology , Cyclization , Enzyme Inhibitors/pharmacokinetics , Enzyme Inhibitors/pharmacology , NF-kappa B/antagonists & inhibitors , Nitriles/pharmacokinetics , Nitriles/pharmacology , Rats , Transcription Factor AP-1/antagonists & inhibitors
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