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Research 361–390 of 475
- 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.
- New approach to 3-oxo-4-aza-5α-androst-1-ene-17β-(--butylcarboxamide)
- Highly efficient nucleophilic addition of alkyl Grignard reagents to 17-ketosteroids in the presence of cerium(III) chloride: Synthesis of 17α-propyl-17β-hydroxy-4-androsten-3-one, an androgen receptor antagonist
- Synthesis and in vitro study of 17β-[N-ureylene-N,N′-disubstituted]-4-methyl-4-aza-5α-androstan-3-ones as selective inhibitors of type I 5α-reductase
- Design, synthesis and biological evaluation of novel 3-oxo-4-oxa-5α-androst-17β-amide derivatives as dual 5α-reductase inhibitors and androgen receptor antagonists
- Crystal Structure of 3-Oxo-4-Aza-5-Alpha-Androstone-17 β-Tert-Butyl Carboxamide with an O···H–(C, N) Acceptor Four-Center Hydrogen Bond
- New Synthesis of Methyl 3β-Hydroxy-5-androstene-17β-carboxylate
- Is 3α, 17β-androstanediol-glucuronide a diagnostic marker in women with androgenic manifestations?
- Nipple Differentiation in Fetal Male Rats Treated with an Inhibitor of the Enzyme 5<i>α</i>-Reductase: Definition of a Selective Role for Dihydrotestosterone*
- Azasteroids as inhibitors of testosterone 5α-reductase in mammalian skin
- Studies of androgen metabolism and action in cultured hair and skin cells
- Expression of steroidogenic enzymes in human sebaceous glands
- New Synthesis of Finasteride
- Improvement of Techniques of Synthesis of Finasteride
- Expression of mRNA for androgen receptor, 5alpha-reductase and 17beta-hydroxysteroid dehydrogenase in human dermal papilla cells
- Three-Month Treatment With a Long-Acting Gonadotropin-Releasing Hormone Agonist of Patients With Benign Prostatic Hyperplasia: Effects on Tissue Androgen Concentration, 5<i>α</i>-Reductase Activity and Androgen Receptor Content*
- More about X‐linked testicular feminization of the mouse as a noninducible (i<sup>s</sup>) mutation of a regulatory locus: 5α‐androstan‐3α‐17ß‐diol as the true inducer of kidney alcohol dehydrogenase and ß‐glucuronidase
- PLASMA C19 STEROID SULPHATE LEVELS AND INDICES OF ANDROGEN BIOAVAILABILITY IN FEMALE PATTERN ANDROGENIC ALOPECIA
- Metabolism of androgens by isolated human beard hair follicles
- Metabolism of androgens by isolated human hair follicles
- Is idiopathic hirsutism idiopathic?
- Studies on neurosteroids XXIV. Determination of neuroactive androgens, androsterone and 5<i>α</i>‐androstane‐3<i>α</i>,17<i>β</i>‐diol, in rat brain and serum using liquid chromatography–tandem mass spectrometry
- Determination Method for Steroid 5α-Reductase Activity Using Liquid Chromatography/Atmospheric Pressure Chemical Ionization–Mass Spectrometry
- Androstanediolglucuronide: A parameter for peripheral androgen activity before and during therapy with cyproterone acetate
- DIABETE E DOLORE: EFFETTO TERAPEUTICO DEI METABOLITI DEL TESTOSTERONE
- Studies on synthesis of finasteride
- Preparation of finasteride by selective dehydrogenation using IBX
- Synthesis of 5α-Reductase Special inhibitor Finasteride
- 17beta Hydroxysteroid Dehydrogenase Type 3 Inhibitors
- Female Androgenic Alopecia