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Research 391–420 of 1000+
- Effect of Solvent on Stereoselectivity in Pd/C (Type 39K)-Catalyzed Hydrogenation of Methyl 3-Oxo-4-aza-5-androstene-17-carboxylate, A Key Intermediate for Finasteride and Dutasteride
- Studies on the efficacy of methyl esters of n-alkyl fatty acids as penetration enhancers
- The Treatment of Alopecia Universalis with Methyl Prednisolone (Medrol)
- New Synthesis of Methyl 3β-Hydroxy-5-androstene-17β-carboxylate
- Prostate-Sparing Effects in Primates of the Potent Androgen 7α-Methyl-19-Nortestosterone: A Potential Alternative to Testosterone for Androgen Replacement and Male Contraception1
- Standard DNA Methylation Analysis in Mouse Epidermis: Bisulfite Sequencing, Methylation-Specific PCR, and 5-Methyl-Cytosine (5mC) Immunological Detection
- Topical SCD-153, a 4-methyl itaconate prodrug, for the treatment of alopecia areata
- Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease
- The synthesis of (−)-4-methyl-8-chloro-trans-1,2,3,4,4a,5,6,10b-octahydrobenzo-[f]-quinolin-3-one-[3-14C] (LY300502-14C]) via a circuitous route
- Acetyl zingerone methyl ether protects hair against oxidative damage incurred during and after treatment with permanent dyes and helps extend longevity of newly developed hair colour
- Synthesis and Pharmacological Evaluation of New 16-Methyl Pregnane Derivatives.
- Response of the Skin of Mice to Methyl Ether of Vitamin A and Vitamin A Palmitate1
- Discovery of 7-Methoxy-6-[4-(4-methyl-1,3-thiazol-2-yl)-1<i>H</i>-imidazol-5-yl]-1,3-benzothiazole (TASP0382088): A Potent and Selective Transforming Growth Factor-β Type I Receptor Inhibitor as a Topical Drug for Alopecia
- 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
- Determination of finasteride, indapamide and tiemonium methyl sulphate using surface plasmon resonance band of silver nanoparticles
- 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.
- DEVELOPING AND VALIDATING AN HPLC METHOD TO QUANTIFY SIMULTANEOUSLY DUTASTERIDE AND THEIR RELATED MOLECULES (DUTASTERIDE ACID, 2,5 BIS- (TRI FLUORO METHYL)-ANILINE AND DUTASTERIDE 17 α-EPIMER) IN CAPSULES
- A Review (Research and Patents) on Jasmonic Acid and Its Derivatives
- Comparison of two encapsulated curcumin particular systems contained in different formulations with regard to<i>in vitro</i>skin penetration
- Benzo[<i>c</i>]quinolizin-3-ones: A Novel Class of Potent and Selective Nonsteroidal Inhibitors of Human Steroid 5α-Reductase 1
- Lessons Learned from the First Decade of Laser-Assisted Drug Delivery
- Histochemical observation of the cell membrane complex of hair.
- Finasteride Topical Delivery Systems for Androgenetic Alopecia
- Mucin‐poor follicular mycosis fungoides
- Treatment-resistant giant unilateral Bowen’s disease of the scalp responding to radiotherapy
- Formulasi dan Evaluasi Sediaan Hair Tonic Anti Alopesia
- A Method to Monitor Dutasteride in Rat Plasma Using Liquid-Liquid Extraction and Multiple Reaction Monitoring: Comparisons and Validation
- Low-level light-assisted photodynamic therapy using a wearable cap-like device for the treatment of actinic keratosis of the scalp
- Elicitor mediated enhancement of wedelolactone in cell suspension culture of Eclipta alba (L.) Hassk
- Synthesis and structure–activity investigation of iodinated arylhydantoins and arylthiohydantoins for development as androgen receptor radioligands