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16-Ketoestrone

From Wikipedia, the free encyclopedia
16-Ketoestrone
Names
IUPAC name
3-Hydroxyestra-1,3,5(10)-triene-16,17-dione
Systematic IUPAC name
(3aS,3bR,9bS,11aS)-7-Hydroxy-11a-methyl-3a,3b,4,5,9b,10,11,11a-octahydro-1H-cyclopenta[a]phenanthrene-1,2(3H)-dione
Other names
16-Oxoestrone; 16-Keto-E1; 16-Oxo-E1; NSC-60462
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
KEGG
UNII
  • InChI=1S/C18H20O3/c1-18-7-6-13-12-5-3-11(19)8-10(12)2-4-14(13)15(18)9-16(20)17(18)21/h3,5,8,13-15,19H,2,4,6-7,9H2,1H3/t13-,14-,15+,18+/m1/s1
    Key: ANPHVANSJXDRTP-BSXFFOKHSA-N
  • C[C@]12CC[C@H]3[C@H]([C@@H]1CC(=O)C2=O)CCC4=C3C=CC(=C4)O
Properties
C18H20O3
Molar mass284.355 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

16-Ketoestrone (16-keto-E1, or16-oxoestrone, or16-oxo-E1) is anendogenousestrogen related to16α-hydroxyestrone and16β-hydroxyestrone.[1][2][3] In contrast to 16α-hydroxyestrone and 16β-hydroxyestrone, but similarly to16-ketoestradiol, 16-ketoestrone is a very weak estrogen with less than 1/1000 theestrogenicpotency ofestrone in theuterus.[3] 16-Ketoestrone has been reported to act as aninhibitor of17β-hydroxysteroid dehydrogenases.[4] 16-Ketoestrone can be converted by16α-hydroxysteroid dehydrogenase intoestriol in the body.[1][5]

References

[edit]
  1. ^abBreuer, Heinz (1962). "The Metabolism of the Natural Estrogens".Vitamins & Hormones.20:285–335.doi:10.1016/S0083-6729(08)60720-7.ISBN 9780127098203.ISSN 0083-6729.
  2. ^Huffman MN, Lott MH (January 1948)."16-Substituted steroids; 16-keto-alpha-estradiol and 16-ketoestrone".J. Biol. Chem.172 (1):325–32.doi:10.1016/S0021-9258(18)35637-0.PMID 18920793.
  3. ^abHuggins C, Jensen EV (September 1955)."The depression of estrone-induced uterine growth by phenolic estrogens with oxygenated functions at positions 6 or 16: the impeded estrogens".J. Exp. Med.102 (3):335–46.doi:10.1084/jem.102.3.335.PMC 2136510.PMID 13252187.
  4. ^Inano H, Tamaoki B (January 1983)."Affinity labeling of arginyl residues at the catalytic region of estradiol 17 beta-dehydrogenase from human placenta by 16-oxoestrone".Eur. J. Biochem.129 (3):691–5.doi:10.1111/j.1432-1033.1983.tb07104.x.PMID 6572146.
  5. ^Stimmel BF, Grollman A, Huffman MN (June 1950)."The metabolism of 16-ketoestrone and 16-keto-estradiol in man".J. Biol. Chem.184 (2):677–85.doi:10.1016/S0021-9258(19)51001-8.PMID 15428451.


Precursors
Corticosteroids
Glucocorticoids
Mineralocorticoids
Sex steroids
Androgens
Estrogens
Progestogens
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ERTooltip Estrogen receptor
Agonists
Mixed
(SERMsTooltip Selective estrogen receptor modulators)
Antagonists
GPERTooltip G protein-coupled estrogen receptor
Agonists
Antagonists
Unknown


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