Structure Database (LMSD)

Common Name
Urocortisone
Systematic Name
3α,17α,21-dihydroxy-5β-pregnane-11,20-dione
Synonyms
  • Tetrahydrocortisone
LM ID
LMST02030098
Formula
C21H32O5
Exact Mass
Calculate m/z
364.224975
Sum Composition
ST 21:2;O5
Status
Active
Show lipids differing only in stereochemistry/bond geometry
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Main

Classification

Category
Main Class
Sub Class
Sterol Lipids [ST]
Steroids [ST02]
C21 steroids (gluco/mineralocorticoids, progestogins) and derivatives [ST0203]

String Representations

InChiKey (Click to copy)
SYGWGHVTLUBCEM-ZIZPXRJBSA-N
InChi (Click to copy)
InChI=1S/C21H32O5/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/h12-15,18,22-23,26H,3-11H2,1-2H3/t12-,13-,14+,15+,18-,19+,20+,21+/m1/s1
SMILES (Click to copy)
[C@@]12([H])CC[C@](O)(C(=O)CO)[C@@]1(C)CC(=O)[C@]1([H])[C@@]3(C)CC[C@@H](O)C[C@@]3([H])CC[C@@]21[H]

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Homo sapiens (#9606)
Mammalia (#40674)
Identification of free tetrahydrocortisone in human peripheral plasma.,
J Clin Endocrinol Metab, 1959
Pubmed ID: 13843459

Other Databases

Wikipedia
Tetrahydrocortisone
KEGG ID
C05470
CHEBI ID
9901
PubChem CID
5866

Calculated Physicochemical Properties

Heavy Atoms 26
Rings 4
Aromatic Rings 0
Rotatable Bonds 2
Van der Waals Molecular Volume 361.09
Topological Polar Surface Area 94.83
Hydrogen Bond Donors 3
Hydrogen Bond Acceptors 5
logP 2.72
Molar Refractivity 96.68

Reactions

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Reactions graph legend

Admin

Created at
-
Updated at
9th Jun 2022