In vitro inhibition of prostaglandin H synthase by compounds from the exocrine secretions of lace bugs

Abstract

1. Selected lace bug-derived and related compounds were shown to be in vitro inhibitors of mammalian and insect derived prostaglandin H synthase. 2. Two compounds, 2,6-dihydroxyacetophenone and 2,4,6-trihydroxyacetophenone, were significantly better inhibitors of prostaglandin synthesis than aspirin, whereas 2-nonyl-5,7-dihydroxychromone and 1-(2,6-dihydroxyphenyl) dodecan-1-one were equivalent to aspirin. 3. 2,4-Dihydroxyacetophenone was less effective in inhibiting the prostaglandin H synthase and 2-nonyl-5-hydroxychromanone showed no inhibition. 4. Three compounds, 2,6-dihydroxyacetophenone, 2,4,6-trihydroxyacetophenone and 1-(2,6-dihydroxyphenyl) dodecan-1-one were equal to aspirin in PSI inhibition with fat body preparations of the American cockroach Periplaneta americana L.