Molecule record

(8S,9S,10R,11S,13S,14S,17R)-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-one

C21H30O5

362.47 g/mol

Loading structure

Molecular properties

Formula
C21H30O5
Molar mass
362.47 g·mol−1
Exact mass
362.2093 Da
7
PubChem CID
5754

Functional groups

Alcohol
Alkane / alkyl carbon
Alkene
Ketone

Physical properties

No source-backed physical properties are curated for this molecule yet.

Common names and synonyms

  • 50-23-7
  • Acticort
  • Alacort
  • Cetacort
  • Cobadex
  • Cort-Dome
  • Cortenema
  • Corticreme
Show all 24 synonyms
  • Cortisol
  • Cremesone
  • Dermacort
  • Efcorbin
  • Eldecort
  • Hycortol
  • Hydrocortisyl
  • Hytone
  • Hytone lotion
  • Incortin-H
  • Kendall's compound F
  • Proctocort
  • Scheroson F
  • Signef
  • Tarcortin
  • hydrocortisone

Structure identifiers

Canonical SMILES
C[C@]12CCC(=O)C=C1CC[C@@H]1[C@@H]2[C@@H](O)C[C@@]2(C)[C@H]1CC[C@]2(O)C(=O)CO
Isomeric SMILES
C[C@]12CCC(=O)C=C1CC[C@@H]3[C@@H]2[C@H](C[C@]4([C@H]3CC[C@@]4(C(=O)CO)O)C)O
InChI
InChI=1S/C21H30O5/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/h9,14-16,18,22,24,26H,3-8,10-11H2,1-2H3/t14-,15-,16-,18+,19-,20-,21-/m0/s1
InChIKey
JYGXADMDTFJGBT-VWUMJDOOSA-N
PubChem CID
5754

Spectroscopy

Tabs appear only for spectra stored with clear provenance.

Open library
No redistributable or simulated spectroscopy record is attached yet.

Simulated NMR

On-demand educational prediction for (8S,9S,10R,11S,13S,14S,17R)-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-one; not experimental data.

Simulated EI mass spectrum

On-demand educational fragmentation for (8S,9S,10R,11S,13S,14S,17R)-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-one; not experimental data.

Sources

Molecule identity

Retrieved 8/20/2026. Reuse status is summarized by the badge; open the source for full details.

Open source record