1997 Volume 20 Issue 5 Pages 490-495
In order to understand the mechanism involved in the aromatase inactivation by androst-5-ene, 4, 7, 17-trione (4), a suicide substrate of aromatase, 5β, 6β-epoxyandrosta-4, 7, 17, 19-tetraone (6) was synthesized as a candidate for a reactive electrophile involved in irreversible binding to the active site of aromatase upon treatment of 19-oxo-5-ene steroid 5 with hydrogen peroxide in the presence of NaHCO3. The epoxide 6 was a competitive inhibitor of human placental aromatase (K1=34 μM); moreover, it inactivated the enzyme in an active-site-directed manner in the absence of NADPH (K1=36 μM, a rate constant for inactivation (kinact)=0.027 min-1). NADPH stimulated the inactivation rate, but the substrate androst-4-ene-3, 17-dione blocked the inactivation. A nucleophile, L-cysteine, did not cause a significant change in the inactivation. When both the epoxide 6 and its 19-methyl analog 7 were subjected separately to a reaction with N-acetyl-L-cycteine in the presence of NaHCO3, the 19-oxo compound 6 disappeared from the reaction mixture more rapidly (t/1/2=6.0 min) than the 19-methyl analog 7 (t1/2=16 min). On the basis of these results, it is suggested that the 5β, 6β-epoxy-19-oxo steroid 6 may be the reactive electrophile that alkylates a nucleophilic residue of the amino acid of the active site.
