CAS 98319-24-5
:3-oxo-4-aza-5A-androstano-17B-(N-terc-butilcarboxamida)
- 17β-(N-tert-Butylcarbamoyl)-4-aza-5α-androstan-3-one
- 3-Oxo-4-Aza-5A-Androstane-17B-(N-T-Butyl)Carboxamide
- (4aR,4bS,6aS,7S,9aS,9bS,11aR)-N-tert-butyl-4a,6a-dimethyl-2-oxohexadecahydro-1H-indeno[5,4-f]quinoline-7-carboxamide
- Androstane-N-terbutyl-3-oxo-4-aza-5 alfa-17 beta-carboxamide
- 17-Beta-(N-Butylcarbamoyl)-4-Aza-5-Alpha-Androstan-3-One
- 17β-(t-Butylcarbamoyl)-4-aza-5a-androstan-3-one
- Dihydroproscar
- N-tert-butyl-3-oxo-4-aza-5α-androst-17β-carboxamide
- Dihydro Finasteride
(4AR,4bS,6aS,7S,9aS,9bS,11aR)-N-(tert-butyl)-4a,6a-dimethyl-2-oxohexadecahydro-1H-indeno[5,4-f]quinoline-7-carboxamide
CAS:Fórmula:C23H38N2O2Pureza:98%Cor e Forma:SolidPeso molecular:374.56003-Oxo-4-aza-5A-androstane-17-β-(N-tert-butylcarboxamide); 98%
CAS:Fórmula:C23H38N2O2Pureza:(HPLC) ≥ 98.0%Cor e Forma:White to off-white powderPeso molecular:374.56Dihydroproscar
CAS:Fórmula:C23H38N2O2Pureza:≥ 95.0% (anhydrous basis)Cor e Forma:White to off-white powderPeso molecular:374.56Finasteride EP Impurity A
CAS:Fórmula:C23H38N2O2Cor e Forma:White To Off-White SolidPeso molecular:374.57N-(1,1-Dimethylethyl)-3-oxo-4-aza-5α-androstane-17β-carboxamide (Dihydrofinasteride)
CAS:Produto ControladoFórmula:C23H38N2O2Cor e Forma:NeatPeso molecular:374.56Dihydro Finasteride
CAS:Impurity Finasteride EP Impurity A
Applications Dihydro Finasteride (Finasteride EP Impurity A) is the reduced product of Finasteride (F342000): a mechanism-based inhibitor of human prostate and skin steroid 5α-reductase. It forms an enzyme-bound NADP-dihydrofinasteride adduct during this inhibitory process.
References Bull, H.G. et al.: Am. J. Chem. Soc., 118, 2359 (1996); Liang, T. et al.: Endocrinol., 117, 571 (1985); Ellsworth, K.P. et al.: J. Steroid Bioche. Mol. Biol., 66, 271 (1998);Fórmula:C23H38N2O2Cor e Forma:Off-WhitePeso molecular:374.56Dihydroproscar
CAS:Dihydroproscar is a synthetic retinoid that is clinically used to treat benign prostatic hyperplasia (BPH). It has been shown to inhibit the synthesis of 3β-hydroxysteroid, which is necessary for the conversion of testosterone to dihydrotestosterone. Dihydroproscar also has a denaturing effect on proteins and inhibits the in vitro synthesis of DNA and RNA. The second-order rate constant for the reaction of dihydroproscar with ribonucleotides is about 1.4 times faster than that for other retinoids. Dihydroproscar has pharmacokinetic properties that are similar to those of other retinoids, including fatty acids and hydrogen chloride.
Fórmula:C23H38N2O2Pureza:Min. 97 Area-%Cor e Forma:PowderPeso molecular:374.56 g/mol3-Oxo-4-aza-5-α-androstane-17-β-N-t-butylcarboxamide
CAS:Fórmula:C23H38N2O2Pureza:98%Cor e Forma:SolidPeso molecular:374.569Ref: 4Z-F-0524
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