A synthetic estrogen receptor agonist
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Active Metabolite(s)
38954Dienestrol
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Diethylstilbestrol

Item No. 10006876

Technical Information
Formal Name
4,4'[(1E)-1,2-diethyl-1,2-ethenediyl]bis-phenol
CAS Number
56-53-1
Molecular Formula
C18H20O2
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
DMF: 30 mg/mlDMSO: 30 mg/mlEthanol: 30 mg/mlEthanol:PBS (pH 7.2)(1:5): .15 mg/ml
λmax
240 nm
SMILES
CC\C(=C(\CC)/c1ccc(O)cc1)\c1ccc(O)cc1
InChi Code
InChI=1S/C18H20O2/c1-3-17(13-5-9-15(19)10-6-13)18(4-2)14-7-11-16(20)12-8-14/h5-12,19-20H,3-4H2,1-2H3/b18-17+
InChi Key
RGLYKWWBQGJZGM-ISLYRVAYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Certificates of Analysis & Batch Specific Data

Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.

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    Product Description

    Diethylstilbestrol (DES) is a synthetic estrogen receptor agonist that was prescribed to pregnant women in the late 1930s. It was banned in 1971 because of possible links to increased risk of breast cancer in mothers along with congenital abnormalities and increased risk of cancer in offspring.1 DES is structurally related to, and is as potent as, estradiol in most assays, with a longer half-life. It has a relative binding affinity to sex hormone binding globulin (SHBG) of 0.2 compared to estradiol which has a relative binding affinity of 100. A concentration of 20 µM DES, displaces 30 ± 13% of 3H-estradiol from SHBG in serum.1,2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Coelingh Bennink, H.J.T. Are all estrogens the same? Maturitas 47(4), 269-275 (2003).

    2. Jury, H.H., Zaxharewski, T.R., and Hammond, G.L. Interactions between human plasma sex hormone-binding globulin and xenobiotic ligands. J. Steroid Biochem. Mol. Biol. 75, 167-176 (2000).