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Estradiol 17β-acetate

From Wikipedia, the free encyclopedia
Chemical compound
Not to be confused withEstradiol acetate.
Pharmaceutical compound
Estradiol 17β-acetate
Clinical data
Drug classEstrogen;Estrogen ester
Identifiers
  • [(8R,9S,13S,14S,17S)-3-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl] acetate
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.110.039Edit this at Wikidata
Chemical and physical data
FormulaC20H26O3
Molar mass314.425 g·mol−1
3D model (JSmol)
  • CC(=O)O[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CCC4=C3C=CC(=C4)O)C
  • InChI=1S/C20H26O3/c1-12(21)23-19-8-7-18-17-5-3-13-11-14(22)4-6-15(13)16(17)9-10-20(18,19)2/h4,6,11,16-19,22H,3,5,7-10H2,1-2H3/t16-,17-,18+,19+,20+/m1/s1
  • Key:QAHOQNJVHDHYRN-SLHNCBLASA-N

Estradiol 17β-acetate is anestrogen and anestrogen ester—specifically, the C17βacetateester ofestradiol—which was never marketed.[1][2][3] It is the C17βpositional isomer of the better-known and clinically usedestradiol esterestradiol acetate (estradiol 3-acetate; Femtrace).[1]

Affinities and estrogenic potencies of estrogen esters and ethers at the estrogen receptors
EstrogenOther namesRBATooltip Relative binding affinity (%)aREP (%)b
ERERαERβ
EstradiolE2100100100
Estradiol 3-sulfateE2S; E2-3S?0.020.04
Estradiol 3-glucuronideE2-3G?0.020.09
Estradiol 17β-glucuronideE2-17G?0.0020.0002
Estradiol benzoateEB; Estradiol 3-benzoate101.10.52
Estradiol 17β-acetateE2-17A31–4524?
Estradiol diacetateEDA; Estradiol 3,17β-diacetate?0.79?
Estradiol propionateEP; Estradiol 17β-propionate19–262.6?
Estradiol valerateEV; Estradiol 17β-valerate2–110.04–21?
Estradiol cypionateEC; Estradiol 17β-cypionate?c4.0?
Estradiol palmitateEstradiol 17β-palmitate0??
Estradiol stearateEstradiol 17β-stearate0??
EstroneE1; 17-Ketoestradiol115.3–3814
Estrone sulfateE1S; Estrone 3-sulfate20.0040.002
Estrone glucuronideE1G; Estrone 3-glucuronide?<0.0010.0006
EthinylestradiolEE; 17α-Ethynylestradiol10017–150129
MestranolEE 3-methyl ether11.3–8.20.16
QuinestrolEE 3-cyclopentyl ether?0.37?
Footnotes:a =Relative binding affinities (RBAs) were determined viain-vitro displacement oflabeledestradiol fromestrogen receptors (ERs) generally ofrodentuterinecytosol.Estrogen esters are variablyhydrolyzed into estrogens in these systems (shorter ester chain length -> greater rate of hydrolysis) and the ER RBAs of the esters decrease strongly when hydrolysis is prevented.b = Relative estrogenic potencies (REPs) were calculated fromhalf-maximal effective concentrations (EC50) that were determined viain-vitroβ‐galactosidase (β-gal) andgreen fluorescent protein (GFP)productionassays inyeast expressing humanERα and humanERβ. Bothmammaliancells and yeast have the capacity to hydrolyze estrogen esters.c = The affinities ofestradiol cypionate for the ERs are similar to those ofestradiol valerate andestradiol benzoate (figure).Sources: See template page.

See also

[edit]

References

[edit]
  1. ^abJunkmann K, Witzel H (1957). "Chemie und Pharmakologie von Steroidhormon-Estern" [Chemistry and pharmacology of steroid hormone esters].Z Vitam Horm Fermentforsch (in German).9 (1–2): 97–143 contd.PMID 13531579.
  2. ^Janocko L, Larner JM, Hochberg RB (April 1984). "The interaction of C-17 esters of estradiol with the estrogen receptor".Endocrinology.114 (4):1180–6.doi:10.1210/endo-114-4-1180.PMID 6705734.
  3. ^Mu Y, Peng S, Zhang A, Wang L (February 2011). "Role of pocket flexibility in the modulation of estrogen receptor alpha by key residue arginine 394".Environ. Toxicol. Chem.30 (2):330–6.Bibcode:2011EnvTC..30..330M.doi:10.1002/etc.389.PMID 21038436.S2CID 22116062.


ERTooltip Estrogen receptor
Agonists
Mixed
(SERMsTooltip Selective estrogen receptor modulators)
Antagonists
GPERTooltip G protein-coupled estrogen receptor
Agonists
Antagonists
Unknown


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