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1 See also  














Template:Structural properties of selected estradiol esters







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  • t
  • e
  • Structural properties of selected estradiol esters
    Estrogen Structure Ester(s) Relative
    mol. weight
    Relative
    E2 contentb
    log Pc
    Position(s) Moiet(ies) Type Lengtha
    Estradiol
    1.00 1.00 4.0
    Estradiol acetate
    C3 Ethanoic acid Straight-chain fatty acid 2 1.15 0.87 4.2
    Estradiol benzoate
    C3 Benzoic acid Aromatic fatty acid – (~4–5) 1.38 0.72 4.7
    Estradiol dipropionate
    C3, C17β Propanoic acid (×2) Straight-chain fatty acid 3 (×2) 1.41 0.71 4.9
    Estradiol valerate
    C17β Pentanoic acid Straight-chain fatty acid 5 1.31 0.76 5.6–6.3
    Estradiol benzoate butyrate
    C3, C17β Benzoic acid, butyric acid Mixed fatty acid – (~6, 2) 1.64 0.61 6.3
    Estradiol cypionate
    C17β Cyclopentylpropanoic acid Cyclic fatty acid – (~6) 1.46 0.69 6.9
    Estradiol enanthate
    C17β Heptanoic acid Straight-chain fatty acid 7 1.41 0.71 6.7–7.3
    Estradiol dienanthate
    C3, C17β Heptanoic acid (×2) Straight-chain fatty acid 7 (×2) 1.82 0.55 8.1–10.4
    Estradiol undecylate
    C17β Undecanoic acid Straight-chain fatty acid 11 1.62 0.62 9.2–9.8
    Estradiol stearate
    C17β Octadecanoic acid Straight-chain fatty acid 18 1.98 0.51 12.2–12.4
    Estradiol distearate
    C3, C17β Octadecanoic acid (×2) Straight-chain fatty acid 18 (×2) 2.96 0.34 20.2
    Estradiol sulfate
    C3 Sulfuric acid Water-soluble conjugate 1.29 0.77 0.3–3.8
    Estradiol glucuronide
    C17β Glucuronic acid Water-soluble conjugate 1.65 0.61 2.1–2.7
    Estramustine phosphated
    C3, C17β Normustine, phosphoric acid Water-soluble conjugate 1.91 0.52 2.9–5.0
    Polyestradiol phosphatee
    C3–C17β Phosphoric acid Water-soluble conjugate 1.23f 0.81f 2.9g
    Footnotes: a = Length of esterincarbon atoms for straight-chain fatty acids or approximate length of ester in carbon atoms for aromaticorcyclic fatty acids. b = Relative estradiol content by weight (i.e., relative estrogenic exposure). c = Experimental or predicted octanol/water partition coefficient (i.e., lipophilicity/hydrophobicity). Retrieved from PubChem, ChemSpider, and DrugBank. d = Also known as estradiol normustine phosphate. e = Polymerofestradiol phosphate (~13 repeat units). f = Relative molecular weight or estradiol content per repeat unit. g = log P of repeat unit (i.e., estradiol phosphate). Sources: See individual articles.
  • Template:Structural properties of major testosterone esters
  • Template:Structural properties of major anabolic steroid esters
  • List of estrogen esters § Estradiol esters

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Template:Structural_properties_of_selected_estradiol_esters&oldid=1174330352"

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    This page was last edited on 7 September 2023, at 19:47 (UTC).

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