Hexestrol Estrogen/progestogen Receptor agonist

Cat.No.S2473

Hexestrol (Bibenzyl) binds to ERα and ERβ with EC50 of 0.07 nM and 0.175 nM, respectively.
Hexestrol Estrogen/progestogen Receptor agonist Chemical Structure

Chemical Structure

Molecular Weight: 270.37

Quality Control

Chemical Information, Storage & Stability

Molecular Weight 270.37 Formula

C18H22O2

Storage (From the date of receipt)
CAS No. 84-16-2 Download SDF Storage of Stock Solutions

Synonyms Bibenzyl Smiles CCC(C1=CC=C(C=C1)O)C(CC)C2=CC=C(C=C2)O

Solubility

In vitro
Batch:

DMSO : 54 mg/mL (199.72 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 54 mg/mL

Water : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
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In vivo Formulation Calculator (Clear solution)

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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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Mechanism of Action

Features
Much higher ERβ binding selectivity than Erα.
Targets/IC50/Ki
ERα [1]
0.07 nM(EC50)
ERβ [1]
0.175 nM(EC50)
In vitro
Hexestrol binds to ERα with EC50 of 0.07 nM and to ERβ with EC50 of 0.175 nM. [1] This compound inhibits activity of AKR1B13 with IC50 of 3.2 μM. [2] It inhibits the d-galactose dehydrogenase activity of thermophilus aldose 1-dehydrogenase with IC50 of 0.063 mM. [3] This chemical inhibits the dehydrogenase activity of AKR1C20 towards 10 μM 4-androsten-3α-o1-17-one with IC50 values of 2.7 μM. [4] It inhibits 17HSD5 with IC50 of 30 μM, and inhibits TBER1 with IC50 of 0.8 μM. [5] This compound reacts with DNA through the catechol quinone, thus can be a carcinogen. [6]
In vivo
Hexestrol administered intraperitoneally at a dose of 6 mg/kg may decrease ovulation in mice, as evident by smaller ovaries and decreased luteal bodies and oocytes. [7]
References
  • [4] https://pubmed.ncbi.nlm.nih.gov/16508162/
  • [5] https://pubmed.ncbi.nlm.nih.gov/16788056/
  • [6] https://pubmed.ncbi.nlm.nih.gov/15650250/

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