Tetrahydrocortisol

CAS: 53-02-1

Ref. TR-T293370

Product Information

• Name: Tetrahydrocortisol
• Synonyms: 2-hydroxy-1-[(3R,5R,8S,9S,10S,11S,13S,14S,17R)-3,11,17-trihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-yl]ethanone, (3Alpha,5Beta,11Beta)-3,11,17,21-Tetrahydroxypregnan-20-One, (3α,5β,11β)-3,11,17,21-Tetrahydroxypregnan-20-one, 3-alpha,11-beta,17,21-Tetrahydroxy-5-beta-pregnan-20-one, 3alpha,11beta,17,21-Tetrahydroxy-5beta-pregnan-20-one, 3alpha,11beta,17,21-Tetrahydroxypregnan-20-one, 3alpha,5beta-Tetrahydrocortisol, 3α,11β,17,21-Tetrahydroxy-5β-pregnan-20-one, 3α,11β,17,21-Tetrol-5β-pregnan-20-one, 3α,11β,17α,21-Tetrahydroxy-5β-pregnan-20-one, 5-beta-Pregnan-20-one, 3-alpha,11-beta,17,21-tetrahydroxy-, 5-beta-Tetrahydrocortisol, 5beta-Pregnan-20-one, 3alpha,11beta,17,21-tetrahydroxy- (8CI), 5beta-Tetrahydrocortisol, 5β-Pregnan-20-one, 3α,11β,17,21-tetrahydroxy-, 5β-Tetrahydrocortisol, Ba 2682, Cortisol, tetrahydro-, Nsc 57431, Pregnan-20-one, 3,11,17,21-tetrahydroxy-, (3alpha,5beta,11beta)- (9CI), Pregnan-20-one, 3,11,17,21-tetrahydroxy-, (3α,5β,11β)-, THF (hormone), Tetrahydro F, Tetrahydrocompound F, Tetrahydrohydrocortisone, Urocortisol
• CAS: 53-02-1

Description

Applications Tetrahydrocortisol is excreted in large amounts in premenopausal patients with early breast cancer. Tetrahydrocortisol has been found to be produced by lymphocytes in both normal and cancer bearing patients however, the concentration of Tetrahydrocortisol has increased in patients with cancer.
References Kodama, M., et. al.: J. Natl. Cancer I., 54, 1275 (1975); Klein, A., et. al.: Metabolism, 27, 731 (1978)

• Brand: TRC

Chemical properties

• Molecular weight: 366.49
• Formula: C₂₁H₃₄O₅
• Color/Form: Off-White
• InChI: InChI=1S/C21H34O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h12-16,18,22-24,26H,3-11H2,1-2H3/t12-,13-,14+,15+,16+,18-,19+,20+,21+/m1/s1
• InChI key: InChIKey=AODPIQQILQLWGS-GXBDJPPSSA-N
• SMILES: C[C@]12CC[C@@H](O)C[C@H]1CC[C@@H]1[C@@H]2[C@@H](O)C[C@@]2(C)[C@H]1CC[C@]2(O)C(=O)CO