CAS 856893-82-8

(8S,13S,17R)-13-ethyl-17-hydroxy-17-(1,1,2,2-tetradeuterioethyl)-1,2,6,7,8,14,15,16-octahydrocyclopenta[a]phenanthren-3-one

Description:

The chemical substance with the name "(8S,13S,17R)-13-ethyl-17-hydroxy-17-(1,1,2,2-tetradeuterioethyl)-1,2,6,7,8,14,15,16-octahydrocyclopenta[a]phenanthren-3-one" and CAS number "856893-82-8" is a synthetic steroid derivative. It features a complex polycyclic structure characteristic of steroids, with multiple chiral centers contributing to its stereochemistry. The presence of an ethyl group and a hydroxy group indicates potential biological activity, possibly influencing its interaction with steroid receptors. The incorporation of deuterium atoms suggests that this compound may be used in studies involving metabolic pathways or pharmacokinetics, as deuterated compounds can provide insights into the behavior of drugs in biological systems. The octahydrocyclopenta[a]phenanthrene core structure is indicative of a specific arrangement of carbon rings, which is crucial for its biological function. Overall, this compound's unique structural features and isotopic labeling make it a valuable candidate for research in medicinal chemistry and pharmacology.

Formula: C₂₁H₂₄D₄O₂

InChI: InChI=1/C21H28O2/c1-3-20-11-9-17-16-8-6-15(22)13-14(16)5-7-18(17)19(20)10-12-21(20,23)4-2/h9,11,13,18-19,23H,3-8,10,12H2,1-2H3/t18-,19?,20+,21+/m1/s1/i2D2,4D2

Tetrahydrogestrinone-d4

Controlled Product

CAS: 856893-82-8

Applications Labelled Tetrahydrogestrinone. Androgen and progestin; hydrogenation product of Gestrinone. (anabolic steroid).
References Labrie, F., et al.: Steroids, 62, 148 (1997), Death, A.K., et al.: J. Clin. Endocrinol. Metab., 89, 2498 (2004), Labrie, F., et al.: J. Endocrinol., 187, 169 (2005), Wang, Y., et al.: Lancet, 365, 671 (2005),

Formula: C₂₁D₄H₂₄O₂

Color and Shape: Neat

Molecular weight: 316.471

Ref: TR-T293602