Journal of Medicinal Chemistry p. 3718 - 3735 (2000)
Update date:2022-09-26
Topics: Inhibitors Chemical Synthesis Structure-Activity Relationship (SAR) Studies Potent Selective Enzyme assay Benzo[c]quinolizin-3-ones Nonsteroidal Cell-based assay
Guarna
Machetti
Occhiato
Scarpi
Comerci, Alessandra
Danza, Giovanna
Mancina, Rosa
Serio, Mario
Hardy, Kimber
The synthesis and biological evaluation of a series of novel, selective inhibitors of isoenzyme 1 of human 5α-reductase (5αR) (EC 1.3.99.5) are reported. The inhibitors are 4aH- (19-29) or 1H-tetrahydrobenzo[c]quinolizin-3-ones (35-47) bearing at position
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(2000)Doi:10.1039/ft9908603191
(1990)Doi:10.1039/b005336h
(2000)Doi:10.1055/s-2007-966047
(2007)Doi:10.1021/ja0030820
(2000)Doi:10.1039/c3ra43307b
(2013)