Evaluation of New Pregnane Derivatives as 5.ALPHA.-Reductase Inhibitor.-Reference-Cited by-同舟云学术

Evaluation of New Pregnane Derivatives as 5.ALPHA.-Reductase Inhibitor.

Published:2001 Issue:5 Volume:49 Page:525-530
ISSN:0009-2363
Container-title:Chemical and Pharmaceutical Bulletin
language:en
Short-container-title:CHEMICAL & PHARMACEUTICAL BULLETIN

Author:

CABEZA Marisa¹,HEUZE Ivonne¹,BRATOEFF Eugene²,RAMIREZ Elena²,MARTINEZ Rosa²

Affiliation:

1. Departments of Biological Systems, Agricultural and Animal Production of the Metropolitan University of Mexico Campus Xochimilco

2. Faculty of Chemistry, National University of Mexico

Publisher

Pharmaceutical Society of Japan

Subject

Drug Discovery,General Chemistry,General Medicine

Link

http://www.jstage.jst.go.jp/article/cpb/49/5/49_5_525/_pdf

Reference19 articles.

1. The Conversion of Testosterone to 5α-Androstan-17β-ol-3-one by Rat Prostate in Vivo and in Vitro

2. Activity of 17β-(N-Alkyl/arylformamido) and 17β-[(N-Alkyl/aryl) alkyl/arylamido]-4-methyl-4-aza-5α-androstan-3-ones as 5α-Reductase Inhibitors in the Hamster Flank Organ and Ear11The research has been supported by Endorecherche that is seeking patent protection for the new compounds. F. Labrie is President of Endorecherche.

3. 3) Raynaud J.P., Azadian-Boulanger B., Bonne C., Perronnet J., Sakis E., Present trends In: Antiandrogen Research in Androgens and Antiandrogens, Martini L, Motta M. Raven Press: New York, 1977, pp. 309-311.

4. 4) Brooks J.R., Harris G.S., Sandler M., Smitter H.J. (eds.) “Design of Enzyme Inhibitors as Drugs,” Vol. 2, Oxford University Press, Oxford, 1994, pp. 495-498.

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