17-epi-Testosterone

CAS : 481-30-1

Ref. TR-T155005

Informations sur le produit

• Nom: 17-epi-Testosterone
• Synonymes: Testosterone Imp. C (EP), Testosterone USP Related Compound C, Testosterone USP RC C, 17alpha-Hydroxyandrost-4-en-3-one, Androst-4-en-3-one, 17-hydroxy-, (17alpha)-, Androst-4-en-3-one, 17alpha-hydroxy- (8CI), (17alpha)-17-Hydroxyandrost-4-en-3-one, 17-Epitestosterone, 17alpha-Hydroxyandrost-4-ene-3-one, 17alpha-Testosterone, 17alpha-cis-Testosterone, 4-Androstene-17alpha-ol-3-one, Androst-4-en-17alpha-ol-3-one, Epitestosterone, Isotestosterone, NSC 26499, Testosterone, cis-, cis-Testosterone, epi-Testosterone, Testosterone Related Compound C, Testosterone Impurity C, (17Alpha)-17-Hydroxyandrost-4-En-3-One, (17α)-17-Hydroxyandrost-4-en-3-one, 17-Alpha-Hydroxyandrost-4-En-3-One, 17α-Hydroxyandrost-4-en-3-one, 17α-Hydroxyandrost-4-ene-3-one, 17α-Testosterone, 17α-cis-Testosterone, 4-Androstene-17α-ol-3-one, Androst-4-en-17α-ol-3-one, Androst-4-en-3-one, 17-hydroxy-, (17α)-, Androst-4-en-3-one, 17α-hydroxy-, Testosterone, cis-

Description

Applications Testosterone and epitestosterone are endogenous steroids that differ in the configuration of the hydroxyl-bearing carbon at C-17. Testosterone is the predominant male sex hormone, whereas the role of epitestosterone is largely unclear. In humans, both androgens are excreted mainly as glucuronide conjugates.
References Wudy, S., et al.: Steroids, 66, 759 (2001), Kootstra, P., et al.: Anal. Chim. Acta., 586, 82 (2007), Sten, T., et al.: Drug Metab. Dispos., 37, 417 (2009),

• Marque: TRC

Propriétés chimiques

• Masse moléculaire: 288.42
• Formule: C₁₉H₂₈O₂
• Couleur/Forme: White To Light Yellow
• InChI: InChI=1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h11,14-17,21H,3-10H2,1-2H3/t14-,15-,16-,17+,18-,19-/m0/s1
• Code InChI: InChIKey=MUMGGOZAMZWBJJ-KZYORJDKSA-N
• SMILES: C[C@]12CC[C@H]3[C@@H](CCC4=CC(=O)CC[C@@]43C)[C@@H]1CC[C@H]2O