Dannhardt G, Kreher M, Nowe U, Schmitt S
Institut für Pharmazie, Johannes Gutenberg-Universität, Fachbereich Chemie und Pharmazie, Mainz, Germany.
Pharmazie. 1997 Jun;52(6):428-36.
A series of 2-aryl-pyrrolobenzothiazoles with additional functional groups was synthesized and characterized. Mainly ring opening and less substitution of the pyrrole moiety was observed reacting the heterocyclic system with diazoethyl acetate. In general all compounds inhibit 5-lipoxygenase more effectively than cyclooxygenase but one of them is a well balanced dual inhibitor. A structure-activity relationship and the enzyme selectivity are discussed.