
Bioorganic and Medicinal Chemistry p. 1481 - 1485 (1996)
Update date:2022-08-05
Topics:
Yamashita, Dennis S.
Holt, Dennis A.
Oh, Hye-Ja
Shah, Dinu
Yen, Hwa-Kwo
Brandt, Martin
Levy, Mark A.
Steroidal 3-carboxy-20-ketones have been prepared within two structural series, the androsta-3,5-dienes and the estra 1,3,5-trienes, as potential inhibitors of types 1 and 2 steroid 5α-reductase, the enzyme activity responsible for the final step in biosynthesis of dihydrotestosterone. These compounds are shown to be potent uncompetitive inhibitors of both human recombinant enzyme activities, defining a novel class of dual steroid 5α-reductase inhibitors.
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