Search
for
Sort by
Research 30 of 1000+
- Novel inhibitors of 5α-reductase
- A concise review- Development of an analytical method and validation of dutasteride
- Recent Advances in Drug Design and Drug Discovery for Androgen- Dependent Diseases
- Species Differences in Prostatic Steroid 5<i>α</i>-Reductases of Rat, Dog, and Human
- 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
- 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.
- 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
- 5α-Reductase Inhibitors, Chemical and Clinical Models
- 12 Treatment of hirsutism with 5α-reductase inhibitors
- Alopecia - the search for novel agents continues
- LY191704: a selective, nonsteroidal inhibitor of human steroid 5 alpha-reductase type 1.
- Steroid Hormones
- In Vivo Time-Dependent Inhibition of Human Steroid 5a-Reductase by Finasteride
- Steroid 5α-Reductase as a Novel Therapeutic Target for Schizophrenia and Other Neuropsychiatric Disorders
- Nonsteroidal inhibitors of human type I steroid 5-.alpha.-reductase
- Synthesis of N-Substituted 3-Oxo-17b- carboxamide-4-aza-5a-androstanes and the Tautomerism of 3-Oxo-4-aza-5-androstenes
- Synthesis and in Vitro Evaluation of 4-Substituted N-(1,1-Dimethylethyl)-3-oxo-4-androstene-17.beta.-carboxamides as 5.alpha.-Reductase Inhibitors and Antiandrogens
- Selective induction of apoptosis in the hamster flank sebaceous gland organ by a topical liposome 5-α-reductase inhibitor: A treatment strategy for acne
- The 5 Alpha-Reductase Isozyme Family: A Review of Basic Biology and Their Role in Human Diseases
- Adrenal steroid precursors exert potent androgenic action in the hamster sebaceous glands of flank organs and ears.
- Synthesis of Spiro[cyclohexane-1,2?-[2H]indene] derivatives as inhibitors of steroid 5?-reductase
- Investigation of intermolecular interactions in finasteride drug crystals in view of X-ray and Hirshfeld surface analysis
- Trends in the Development of New Drugs for Treatment of Benign Prostatic Hyperplasia
- Finasteride for prostatic disease: an updated and comprehensive review
- Recent advances in thiasteroids chemistry
- In vitro and In vivo Effects of 17β-N-(4-phenylcarbamoyl) androst-4-en-3- one Derivatives as 5a-reductase Inhibitors on Androgen-dependent Glands
- 5-α-Reductase inhibitors for prostate cancer chemoprevention: an updated Cochrane systematic review
- Pharmacophore and Atom Based 3D QSAR Studies on the Novel 5-Alpha-Reductase Inhibitors
- The multiple uses of azelaic acid in dermatology: mechanism of action, preparations, and potential therapeutic applications
- Molecular Interactions of New Pregnenedione Derivatives