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Biological Data Biological description Estrogen receptor (ER) agonist (Ki values are 0.13 and 0.12 nM at ERα and ERβ respectively). Also shows activity at GPR30 receptors (Ki = 6 nM). Endogenous hormone. Shows neuroprotective and antioxidant effects.
Solubility & Handling Storage instructions Room temperature
Solubility overview Soluble in DMSO (100 mM) and in ethanol (75 mM)
Important This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.
Chemical Data Chemical name (8R,9S,13S,14S,17S)-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,17-diol
Chemical structure
Molecular Formula C18 H24 O2
SMILES C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2O)CCC4=C3C=CC(=C4)O
InChi InChI=1S/C18H24O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-17,19-20H,2,4,6-9H2,1H3/t14-,15-,16+,17+,18+/m1/s1
InChiKey VOXZDWNPVJITMN-ZBRFXRBCSA-N
References for 17 β-Estradiol References are publications that support the biological activity of the product
The ins and outs of GPR30: a transmembrane estrogen receptor. Prossnitz ER et al (2008) J Steroid Biochem Mol Biol 109(3-5) : 350-3. Identity of an estrogen membrane receptor coupled to a G protein in human breast cancer cells. Thomas P et al (2005) Endocrinology 146(2) : 624-32. Comparison of the ligand binding specificity and transcript tissue distribution of estrogen receptors alpha and beta. Kuiper GG et al (1997) Endocrinology 138(3) : 863-70. 17-beta estradiol protects neurons from oxidative stress-induced cell death in vitro. Behl C et al (1995) Biochem Biophys Res Commun 216(2) : 473-82.
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Estrogen receptor (ER) agonist