
CAS 4993-32-2: Estr-5(10)-ene-3β,17β-diol
Formula:C18H28O2
InChI:InChI=1S/C18H28O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h12,14-17,19-20H,2-10H2,1H3/t12-,14+,15+,16-,17-,18-/m0/s1
InChI key:InChIKey=IBHQSODTBQCZDA-MACGOEAWSA-N
SMILES:C[C@@]12[C@]([C@]3([C@@](C4=C(CC3)C[C@@H](O)CC4)(CC1)[H])[H])(CC[C@@H]2O)[H]
Synonyms:- Estr-5(10)-ene-3β,17β-diol
- (3β,17β)-Estr-5(10)-ene-3,17-diol
- 3β,17β-Dihydroxy-19-norandrost-5(10)-ene
- Estr-5(10)-ene-3,17-diol, (3β,17β)-
- See more synonyms
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Found 3 products.
3beta-Dihydroxy-19-norandrost-5(10)-ene
CAS:Controlled ProductApplications 3β-Dihydroxy-19-norandrost-5(10)-ene is an intermediate in the synthesis of 3β,17β-Dihydroxy-19-norandrost-5(10)-ene (D453800), which is a metabolite of Androstenedione. A novel 19-norsteroid, from androstenedione and 19-hydroxyandrostenedione by cultured porcine granulosa cells is reported for the first time. References Haarbo, J., et al.: Clin. Physiol., 11, 331 (1991), Krebs-Smith, S., et al.: Eur. J. Clin. Nutr., 54, 281(2000), Rasmussen, B., et al.: J. Clin. Endocrinol. Metab., 85, 55 (2000),Formula:C18H28O2Color and Shape:NeatMolecular weight:276.413beta-17beta-Dihydroxy-19-norandrost-5(10)-ene
CAS:Controlled ProductApplications A metabolite of Androstenedione. A novel 19-norsteroid, from androstenedione and 19-hydroxyandrostenedione by cultured porcine granulosa cells is reported for the first time. References Haarbo, J., et al.: Clin. Physiol., 11, 331 (1991), Krebs-Smith, S., et al.: Eur. J. Clin. Nutr., 54, 281(2000), Rasmussen, B., et al.: J. Clin. Endocrinol. Metab., 85, 55 (2000),Formula:C18H28O2Color and Shape:Beige To Light BrownMolecular weight:276.413b,17b-Dihydroxy-19-norandrost-5(10)-ene
CAS:Controlled Product3b,17β-Dihydroxy-19-norandrost-5(10)-ene is a metabolite of oestrone and is converted to 3β-hydroxysteroid dehydrogenase (3βHSD) by an interaction with 17β-hydroxysteroid dehydrogenase (17βHSD). 3b,17β-Dihydroxy-19-norandrost-5(10)-ene has been shown to be involved in the progression of hepatic steatosis. It also has a role in depression and may have antiviral properties. 3b,17β-Dihydroxy-19-norandrost-5(10)-ene is synthesized from progesterone and 17α hydroxylase via 17,20 lyase. The reaction product to this synthesis is progesterone. The conversion of 3b,17β-dihydroxy 19nortestosterone to 3b,17βFormula:C18H28O2Purity:Min. 95%Molecular weight:276.41 g/mol