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Product Description
Mechanism of Action
Micronized finasteride enhances dissolution and absorption. Finasteride inhibits 5‑alpha reductase type II, reducing dihydrotestosterone (DHT) formation and modulating androgen‑responsive tissues.
Benefits and Advantages
Used in androgen‑pathway research, prostate‑biology studies and hair‑follicle DHT suppression modelling.
Side Effects and Risks
Risks include sexual dysfunction, mood changes and hormonal disturbances.
Datasheet
| Molecular Formula | C23H36N2O2 |
|---|---|
| Molecular Weight | 372.55 g/mol |
| CAS Number | 98319-26-7 |
| Storage Condition | Store in a cool, dry place; protect from light |
| Solubility | Soluble in water |
| Purity | Purity information is available upon request (COA). |
| Synonym | 4a,6a-Dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-indeno(5,4-f)quinoline-7-carboxylic acid tert-butylamide; 4a,6a-Dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-indeno[5,4-f]quinoline-7-carboxylic acid tert-butylamide; RefChem:1071733; 1212235-84-1; N-tert-butyl-4a,6a-dimethyl-2-oxo-2,4a,4b,5,6,6a,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-indeno[5,4-f]quinoline-7-carboxamide |
| IUPAC/Chemical Name | (17β)-N-tert-butyl-carbamoyl-4-aza-5α-androst-1-en-3-one |
| InChl Key | Unavailable |
| InChl Code | Unavailable |
| References | PubChem; ChemBL; FDA; |
3D Conformer.
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