CAS 514-61-4
:Metilnortestosterona
- (17Beta)-17-Hydroxy-17-Methylestr-4-En-3-One
- (17β)-17-Hydroxy-17-methylestr-4-en-3-one
- 13β,17α-Dimethyl-17-hydroxygon-4-en-3-one
- 17-Hydroxy-17-Methylestr-4-En-3-One
- 17-Methyl-19-nortestosterone
- 17α-Methyl-17β-hydroxy-4-estrene-3-one
- 17α-Methyl-17β-hydroxy-Δ<sup>4</sup>-estren-3-one
- 17α-Methyl-19-nortestosterone
- 17α-Methyl-3-oxo-4-estren-17β-ol
- 17α-Methyl-4-estren-17β-ol-3-one
- 17α-Methylestra-4-en-17-ol-3-one
- 17α-Methylestrenolone
- 17β-Hydroxy-17-methylestr-4-en-3-one
- 17β-Hydroxy-17α-methylestr-4-en-3-one
- 19-Normethisterone
- Estr-4-en-3-one, 17-hydroxy-17-methyl-, (17β)-
- Estr-4-en-3-one, 17β-hydroxy-17-methyl-
- Lutenin
- Matronal
- Metalutin
- Methalutin
- Methylestrenolone
- Methylnortestosterone
- Methyloestrenolone
- NSC 10039
- Normetandrone
- Normethandrolone
- Normethandrone
- Normethanedrolone
- Normethisterone
- Orgasteron
- Ver más sinónimos
4-Estren-17α-methyl-d3-17β-ol-3-one
CAS:Producto controladoPureza:99 atom % DForma y color:White SolidPeso molecular:291.45Normethandrone
CAS:Producto controladoApplications Androgen. Controlled substance (anabolic steroid).
References Matias, P., et al.: J. Biol. Chem., 275, 26164 (2000), Fang, H., et al.: Chem. Res. Toxicol., 16, 1338 (2003), Raudrant, D., et al.: Drugs 63, 463 (2003), Death, A., et al.: Steroids, 70, 946 (2005),Fórmula:C19H28O2Forma y color:White To Off-WhitePeso molecular:288.42Normethandrone-d3
CAS:Producto controladoApplications Labelled Normethandrone. Androgen. Controlled substance (anabolic steroid).
References Matias, P., et al.: J. Biol. Chem., 275, 26164 (2000), Fang, H., et al.: Chem. Res. Toxicol., 16, 1338 (2003), Raudrant, D., et al.: Drugs 63, 463 (2003), Death, A., et al.: Steroids, 70, 946 (2005),Fórmula:C19D3H25O2Forma y color:NeatPeso molecular:291.44317alpha-Methyl-19-nortestosterone
CAS:Producto controlado17alpha-Methyl-19-nortestosterone (17MT) is an anti-cancer agent that has been used as a contraceptive. It inhibits the conversion of testosterone to dihydrotestosterone by competitive inhibition of the enzyme 3beta-hydroxysteroid dehydrogenase, which is responsible for the first step in the biosynthesis of androgens. 17MT has also been shown to inhibit angiotensin II formation, thereby reducing blood pressure. This drug acts as a structural analogue of progesterone and binds to progesterone receptors, as well as other steroid receptors, with high affinity. 17MT also inhibits fatty acid synthesis in cancer cells, leading to decreased tumor growth.
Fórmula:C19H28O2Pureza:Min. 95%Forma y color:PowderPeso molecular:288.42 g/molNormethandrone (1 mg/ml in Acetonitrile)
CAS:Producto controladoFórmula:C19H28O2Forma y color:Single SolutionPeso molecular:288.42


