Home Cart Sign in  
Chemical Structure| 84-16-2 Chemical Structure| 84-16-2

Structure of Hexestrol
CAS No.: 84-16-2

Chemical Structure| 84-16-2

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

Hexestrol can bind to ERα and ERβ selectively with EC50 of 0.07 nM and 0.175 nM respectively.

Synonyms: meso-Hexestrol; Bibenzyl; Sinestrol

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

DE Stock

US Stock

Asia Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of Hexestrol

CAS No. :84-16-2
Formula : C18H22O2
M.W : 270.37
SMILES Code : CC[C@H](C1=CC=C(O)C=C1)[C@H](C2=CC=C(O)C=C2)CC
Synonyms :
meso-Hexestrol; Bibenzyl; Sinestrol
MDL No. :MFCD00068996
InChI Key :PBBGSZCBWVPOOL-HDICACEKSA-N
Pubchem ID :192197

Safety of Hexestrol

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H315-H319-H332
Precautionary Statements:P280-P305+P351+P338

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
mouse oocyte 100 μM To assess the effect of HES on oocyte maturation, results showed that HES exposure significantly reduced the capacity of oocyte maturation Front Cell Dev Biol. 2021 Jul 6;9:708980

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Rats Adrenal cortex inhibition model Subcutaneous injection 0.4 mg/kg Once daily for 4-6 days To study the inhibitory effect of Hexoestrol on adrenal cortical secretion in rats and its restoration mechanisms. J Physiol. 1957 Oct 30;138(3):460-72
Guinea-pigs Adult guinea-pigs Subcutaneous injection 20 mg/kg Once daily for 5 days To study the effect of hexoestrol on adrenocortical secretion. Results showed that hexoestrol caused a significant fall in adrenal cholesterol content, reduced cortisol secretion rate, but increased cortisol concentration in peripheral blood. J Physiol. 1963 Nov;169(2):373-85
Rats Normal and Hexestrol-treated rats Subcutaneous injection 0.37-0.5 mg/kg/day Once daily for 3 to 15 days To investigate the inhibitory effect of Hexestrol on adrenocortical secretion in rats. Results showed that Hexestrol-treated rats had significantly reduced corticosterone secretion, averaging 31% of normal. J Physiol. 1955 Dec 29;130(3):601-14
Mice Adult female mice Oral gavage 6 mg/kg/day Once daily for 1 month To evaluate the effect of HES on ovarian function and folliculogenesis, results showed that HES exposure significantly reduced ovary weight and impaired ovary structure Front Cell Dev Biol. 2021 Jul 6;9:708980

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.70mL

0.74mL

0.37mL

18.49mL

3.70mL

1.85mL

36.99mL

7.40mL

3.70mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
Protocol 2

References

[1]Waibel M, De Angelis M, et al. Bibenzyl- and stilbene-core compounds with non-polar linker atom substituents as selective ligands for estrogen receptor beta. Eur J Med Chem. 2009 Sep;44(9):3412-24.

[2]Endo S, Matsunaga T, et al. Characterization of a rat NADPH-dependent aldo-keto reductase (AKR1B13) induced by oxidative stress. Chem Biol Interact. 2009 Mar 16;178(1-3):151-7.

[3]Waibel M, De Angelis M, Stossi F, Kieser KJ, Carlson KE, Katzenellenbogen BS, Katzenellenbogen JA. Bibenzyl- and stilbene-core compounds with non-polar linker atom substituents as selective ligands for estrogen receptor beta. Eur J Med Chem. 2009 Sep;44(9):3412-24

[4]Endo S, Matsunaga T, Mamiya H, Hara A, Kitade Y, Tajima K, El-Kabbani O. Characterization of a rat NADPH-dependent aldo-keto reductase (AKR1B13) induced by oxidative stress. Chem Biol Interact. 2009 Mar 16;178(1-3):151-7

[5]Asada Y, Endo S, Inoue Y, Mamiya H, Hara A, Kunishima N, Matsunaga T. Biochemical and structural characterization of a short-chain dehydrogenase/reductase of Thermus thermophilus HB8: a hyperthermostable aldose-1-dehydrogenase with broad substrate specificity. Chem Biol Interact. 2009 Mar 16;178(1-3):117-26

[6]Matsumoto K, Endo S, Ishikura S, Matsunaga T, Tajima K, El-Kabbani O, Hara A. Enzymatic properties of a member (AKR1C20) of the aldo-keto reductase family. Biol Pharm Bull. 2006 Mar;29(3):539-42

[7]Ishikura S, Matsumoto K, Sanai M, Horie K, Matsunaga T, Tajima K, El-Kabbani O, Hara A. Molecular cloning of a novel type of rat cytoplasmic 17beta-hydroxysteroid dehydrogenase distinct from the type 5 isozyme. J Biochem. 2006 Jun;139(6):1053-63

[8]de Oliveira JM, Simões MJ, Mora OA, Simões RS, Oliveira-Filho RM, Oliveira PB, Baracat EC, Soares JM Jr. Effects of hexestrol on mouse ovarian morphology and ovulation. Maturitas. 2008 Jun 20;60(2):153-7

 

Historical Records

Categories