Design, Synthesis, and Biological Evaluation of Phenylamino-Substituted
6,11-Dihydro-dibenzo[b,e]oxepin-11-ones and Dibenzo[a,d]cycloheptan-5-ones: Novel p38 MAP
Kinase Inhibitors
posted on 2006-12-28, 00:00authored byStefan A. Laufer, Gabriele M. Ahrens, Solveigh C. Karcher, Jörg S. Hering, Raimund Niess
The pathogenesis of chronic inflammatory diseases is promoted by various pro-inflammatory cytokines.
p38 MAP kinase seems to be a valid target as it controls proinflammatory cytokine levels on both
transcriptional and translational levels. Starting from benzophenone-type inhibitors, a rigidisation strategy
lead to 3-amino-6,11-dihydro-dibenzo[b,e]thiepin-11-one, phenylamino-substituted 6,11-dihydro-dibenzo[b,e]oxepin-11-ones, and dibenzo[a,d]cyclohepten-5-ones. Synthesis, p38 inhibition, and CYP-inhibition of
selected compounds are described.