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Inhibitors of the arachidonic acid cascade: interfering with multiple pathways
Karin Meirer1, Dieter Steinhilber, Ewgenij Proschak
1Institute of Pharmaceutical Chemistry, OSF/ZAFES/TMP, Goethe-University of Frankfurt, Frankfurt, Germany.
Abstract:
Modulators of the arachidonic acid cascade have been in the focus of research for treatments of inflammation and pain for several decades. Targeting this complex pathway experiences a paradigm change towards the design and development of multi-target inhibitors, exhibiting improved efficacy and less undesired side effects. This minireview summarizes recent developments in the field of designed multi-target ligands of the arachidonic acid cascade. In addition to the well-known dual inhibitors of 5-lipoxygenase and cyclooxygenase-2 such as licofelone, very recent developments are discussed. Especially, multi-target inhibitors interfering with the cytochrome P450 pathway via inhibition of soluble epoxide hydrolase seem to offer a novel opportunity for development of novel anti-inflammatory drugs.
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