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16-Epiestriol
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16-Epiestriol

CAS: 547-81-9

Ref. 3D-FE22724

1mg
112.00 €
2mg
178.00 €
5mg
316.00 €
10mg
395.00 €
25mg
694.00 €
Estimated delivery in United States, on Friday 26 Jul 2024

Product Information

Name:
16-Epiestriol
Controlled Product
Synonyms:
  • (16β,17β)-Estra-1,3,5(10)-triene-3,16,17-triolEstra-1,3,5(10)-triene-3,16β,17β-triol
  • (16Beta,17Beta)-Estra-1,3,5(10)-Triene-3,16,17-Triol
  • (16β,17β)-Estra-1,3,5(10)-triene-3,16,17-triol
  • 16-Epiestratriol
  • 16-epi-Estriol
  • 16β,17β-Estriol
  • 16β-Hydroxyestradiol
  • Actriol
  • Epiestriol
  • Epioestriol
  • See more synonyms
  • Estra-1,3,5(10)-triene-3,16,17-triol, (16β,17β)-
  • Estra-1,3,5(10)-triene-3,16β,17-triol
  • Estra-1,3,5(10)-triene-3,16β,17β-triol
  • NSC 26646
Description:

16-Epiestriol is a natural estrogen that can be found in urine samples. It has been shown to bind to the glucocorticoid receptor, which plays an important role in the regulation of immune responses and metabolism. 16-Epiestriol has also been shown to have immunosuppressive activities and may be used to treat cancer. 16-Epiestriol is metabolized by esterases in the liver, which leads to the production of covalent adducts. These covalent adducts bind to proteins in human liver and other tissues, leading to potential carcinogenicity. 16-Epiestriol binds with high affinity to streptococcus faecalis, which is an opportunistic pathogen associated with urinary tract infections. The optimum pH for this drug is 8.5 and it has been shown that it does not bind well at pH levels below 7 or above 11.

Notice:
Our products are intended for lab use only. For any other use, please contact us.
Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Molecular weight:
288.38 g/mol
Formula:
C18H24O3
Purity:
Min. 95%
Color/Form:
Powder
MDL:
Melting point:
Boiling point:
Flash point:
Density:
Concentration:
EINECS:
Merck:
HS code:

Hazard Info

UN Number:
EQ:
Class:
H Statements:
P Statements:
Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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