18 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
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Dual-acting agents with alpha1-adrenoceptor antagonistic and steroid 5alpha-reductase inhibitory activities. Synthesis and evaluation of arylpiperazine derivatives.
Zeria Pharmaceutical
Synthesis of benzanilide derivatives as dual acting agents with alpha 1-adrenoceptor antagonistic action and steroid 5-alpha reductase inhibitory activity.
Zeria Pharmaceutical
A practical synthesis of 3-substituted delta 3,5(6)-steroids as new potential 5 alpha-reductase inhibitor.
Chinese Academy of Science
Steroidal A ring aryl carboxylic acids: a new class of steroid 5 alpha-reductase inhibitors.
Smith Kline & French Laboratories
Synthesis and evaluation of 2'-substituted 4-(4'-carboxy- or 4'-carboxymethylbenzylidene)-N-acylpiperidines: highly potent and in vivo active steroid 5alpha-reductase type 2 inhibitors.
Saarland University
Indole derivatives as a new class of steroid 5 alpha-reductase inhibitors.
Kyowa Hakko Kogyo
Structure-activity relationships for inhibition of type 1 and 2 human 5 alpha-reductase and human adrenal 3 beta-hydroxy-delta 5-steroid dehydrogenase/3-keto-delta 5-steroid isomerase by 6-azaandrost-4-en-3-ones: optimization of the C17 substituent.
Glaxo Inc. Research Institute
Azasteroids: structure-activity relationships for inhibition of 5 alpha-reductase and of androgen receptor binding.
TBA
Structure activity relationship study of known inhibitors of the enzyme 5 alpha-reductase (5AR).
Kingston University
Recent advances on synthesis and biological activities of C-17 aza-heterocycle derived steroids.
Changzhi University
Fluorine and Fluorinated Motifs in the Design and Application of Bioisosteres for Drug Design.
Bristol-Myers Squibb
Synthesis and 5 alpha-reductase inhibitory activities of benzofuran derivatives with a carbamoyl group.
Sankyo
Novel lead generation through hypothetical pharmacophore three-dimensional database searching: discovery of isoflavonoids as nonsteroidal inhibitors of rat 5 alpha-reductase.
TBA
(E)-4-(2-[[3-(indol-5-yl)-1-oxo-2-butenyl]amino]phenoxy)butyric acid derivatives: a new class of steroid 5 alpha-reductase inhibitors in the rat prostate. 1.
Kyowa Hakko Kogyo
Hydroxyperfluoroazobenzenes: novel inhibitors of enzymes of androgen biosynthesis.
Institute of Cancer Research