
Bioorganic and Medicinal Chemistry Letters p. 1335 - 1340 (1999)
Update date:2022-08-11
Topics:
Higuchi, Robert I.
Edwards, James P.
Caferro, Thomas R.
Ringgenberg, Josef D.
Kong, James W.
Hamann, Lawrence G.
Arienti, Kristen L.
Marschke, Keith B.
Davis, Robert L.
Farmer, Luc J.
Jones, Todd K.
A series of human androgen receptor (hAR) agonists based on 4-alkyl-; 4,4-dialkyl-; and 3,4-dialkyl-1,2,3,4-tetrahydro-8-pyridono[5,6-g]quinoline was synthesized and evaluated in competitive receptor binding assays and an androgen receptor cotransfection assay in a mammalian cell background. A number of compounds in this series demonstrated activity equal to or better than dihydrotestosterone in both assays and represent a novel class of compounds for use in androgen replacement therapy.
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