16-Hydroxydehydroepiandrosterone

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16-Hydroxydehydroepiandrosterone
16-hydroxydehydroepiandrosterone.png
16-Hidroxidehidroepiandrosterona3D.png
Names
IUPAC name
(3S,8R,9S,10R,13S,14S,16R)-3,16-Dihydroxy-10,13-dimethyl-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-one
Other names
3β,16α-Dihydroxyandrost-5-en-17-one
Identifiers
1232-73-1 N
ChEBI CHEBI:27771 YesY
ChemSpider 92168 YesY
Jmol 3D model Interactive image
PubChem 102030
  • InChI=1S/C19H28O3/c1-18-7-5-12(20)9-11(18)3-4-13-14(18)6-8-19(2)15(13)10-16(21)17(19)22/h3,12-16,20-21H,4-10H2,1-2H3/t12-,13+,14-,15-,16+,18-,19-/m0/s1 YesY
    Key: QQIVKFZWLZJXJT-DNKQKWOHSA-N YesY
  • InChI=1/C19H28O3/c1-18-7-5-12(20)9-11(18)3-4-13-14(18)6-8-19(2)15(13)10-16(21)17(19)22/h3,12-16,20-21H,4-10H2,1-2H3/t12-,13+,14-,15-,16+,18-,19-/m0/s1
    Key: QQIVKFZWLZJXJT-DNKQKWOHBQ
  • O=C3[C@]2(CC[C@@H]1[C@@]4(C(=C/C[C@H]1[C@@H]2C[C@H]3O)\C[C@@H](O)CC4)C)C
Properties
C19H28O3
Molar mass 304.42 g/mol
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

16-Hydroxydehydroepiandrosterone (16-OH-DHEA) is an endogenous metabolite of dehydroepiandrosterone (DHEA). In its sulfonated form (16-Hydroxydehydroepiandrosterone sulfate or 16-OH DHEA-S), it is an intermediate in the biosynthesis of estriol.[1]

16-OH-DHEA has estrogenic actions.[2]

References

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



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