Hexestrol 是非甾体合成雌激素，对雌激素受体ERα和ERβ的Ki=均为 0.06 nM。它可增加牛的体重，也可用于雌激素缺乏引起的疾病的研究。

Hexestrol binds to ERα and ERβ with EC50 of 0.07 nM and 0.175 nM, respectively.

Hexestrol binds to ERα with EC50 of 0.07 nM and to ERβ with EC50 of 0.175 nM. [1] Hexestrol inhibits activity of AKR1B13 with IC50 of 3.2 μM. [2] Hexestrol inhibits the d-galactose dehydrogenase activity of thermophilus aldose 1-dehydrogenase with IC50 of 0.063 mM. [3] Hexestrol inhibits the dehydrogenase activity of AKR1C20 towards 10 μM 4-androsten-3α-o1-17-one with IC50 values of 2.7 μM. [4] Hexestrol inhibits 17HSD5 with IC50 of 30 μM, and inhibits TBER1 with IC50 of 0.8 μM. [5] Hexestrol reacts with DNA through the catechol quinone, thus can be a carcinogen. [6]

Hexestrol administered intraperitoneally at dose of 6 mg/kg may decrease ovulation in mice, as evident by smaller ovaries and decreased luteal bodies and oocytes. [7]

84-16-2

C18H22O2

270.372

Bibenzyl;meso-Hexestrol;Hexanoestrol;Hexestrofen;4,4'-(1,2-二乙基亚乙基)二苯酚

DMSO:39 mg/mL (144.2 mM)
H2O:<1 mgml
Ethanol:39 mg/mL (144.2 mM)
Powder: -20°C for 3 years
In solvent: -80°C for 2 years