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17α-Epiestriol

17α-Epiestriol

17α-Epiestriol, or simply 17-epiestriol, also known as 16α-hydroxy-17α-estradiol or estra-1,3,5(10)-triene-3,16α,17α-triol, is a minor and weak endogenous estrogen, and the 17α-epimer of estriol (which is 16α-hydroxy-17β-estradiol). It is formed from 16α-hydroxyestrone. In contrast to other endogenous estrogens like estradiol, 17α-epiestriol is a selective agonist of the ERβ. It is described as a relatively weak estrogen, which is in accordance with its relatively low affinity for the ERα. 17α-Epiestriol has been found to be approximately 400-fold more potent than estradiol in inhibiting tumor necrosis factor α (TNFα)-induced vascular cell adhesion molecule 1 (VCAM-1) expression in vitro.

See also Epimestrol 16β,17α-Epiestriol 16β-Epiestriol 17α-Estradiol 2-Methoxyestradiol

References

Tags

  • Biochemistry stubs
  • Estrane stubs
  • Estranes
  • Estrogens
  • Hormones of the hypothalamus-pituitary-gonad axis
  • Selective ERβ agonists
  • Sex hormones