
Bioorganic and Medicinal Chemistry Letters p. 2839 - 2844 (1998)
Update date:2022-08-11
Topics:
Duncia, John V.
Santella III, Joseph B.
Higley, C. Anne
Pitts, William J.
Wityak, John
Frietze, William E.
Rankin, F. Wayne
Sun, Jung-Hui
Earl, Richard A.
Tabaka, A. Christine
Teleha, Christopher A.
Blom, Karl F.
Favata, Margaret F.
Manos, Elizabeth J.
Daulerio, Andrea J.
Stradley, Deborah A.
Horiuchi, Kurumi
Copeland, Robert A.
Scherle, Peggy A.
Trzaskos, James M.
Magolda, Ronald L.
Trainor, George L.
Wexler, Ruth R.
Hobbs, Frank W.
Olson, Richard E.
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 μM for MEK 1 and 0.06 μM 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.
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