Androstanedione

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Not to be confused with androstenedione.
Androstanedione
5alpha-Androstanedione.svg
5α-Androstanedione
5beta-Androstanedione.svg
5β-Androstanedione
Names
Systematic IUPAC name
Androstane-3,17-dione
Other names
Dihydroandrostenedione;
etiocholane-3,17-dione
Identifiers
5982-99-0 (α/β) YesY
846-46-8 (α) YesY
1229-12-5 (β) YesY
ChEBI CHEBI:22542
ChemSpider 2299204 (α/β)
Jmol 3D model Interactive image
PubChem 3034809 (α/β)
  • InChI=1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12,14-16H,3-11H2,1-2H3/t12?,14-,15-,16-,18-,19-/m0/s1
    Key: RAJWOBJTTGJROA-RNQTWYFASA-N
  • InChI=1/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12,14-16H,3-11H2,1-2H3/t12?,14-,15-,16-,18-,19-/m0/s1
    Key: RAJWOBJTTGJROA-RNQTWYFABO
  • O=C4CC3CC[C@@H]2[C@H](CC[C@@]1(C(=O)CC[C@H]12)C)[C@@]3(C)CC4
Properties
C19H28O2
Molar mass 288.43 g·mol−1
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Androstanediones are a pair of isomeric steroids which differ at the 5-position. They are distinguished as 5α-androstanedione and 5β-androstanedione. In humans, 5α-androstanedione is a metabolic precursor of both testosterone and estrone.[1]

See also

References

  1. ↑ Lua error in package.lua at line 80: module 'strict' not found.



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