CAS 514-61-4
:Methylnortestosteron
- (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
- Weitere Synonyme anzeigen
4-Estren-17α-methyl-d3-17β-ol-3-one
CAS:Kontrolliertes ProduktReinheit:99 atom % DFarbe und Form:White SolidMolekulargewicht:291.45Normethandrone
CAS:Kontrolliertes ProduktApplications 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),Formel:C19H28O2Farbe und Form:White To Off-WhiteMolekulargewicht:288.42Normethandrone-d3
CAS:Kontrolliertes ProduktApplications 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),Formel:C19D3H25O2Farbe und Form:NeatMolekulargewicht:291.44317alpha-Methyl-19-nortestosterone
CAS:Kontrolliertes Produkt17alpha-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.
Formel:C19H28O2Reinheit:Min. 95%Farbe und Form:PowderMolekulargewicht:288.42 g/molNormethandrone (1 mg/ml in Acetonitrile)
CAS:Kontrolliertes ProduktFormel:C19H28O2Farbe und Form:Single SolutionMolekulargewicht:288.42


