CAS 547-81-9
:16-epiestriol
Description:
16-Epiestriol is a naturally occurring steroid and a derivative of estriol, which is a type of estrogen. It is characterized by its molecular structure, which includes a steroid backbone with specific functional groups that contribute to its biological activity. This compound is primarily known for its role in the endocrine system, particularly in relation to female reproductive health. It exhibits estrogenic activity, influencing various physiological processes such as menstrual cycle regulation and reproductive system function. The chemical formula of 16-epiestriol reflects its composition of carbon, hydrogen, and oxygen atoms, typical of steroid hormones. Its CAS number, 547-81-9, is a unique identifier used to facilitate the identification of this substance in chemical databases. In research and clinical settings, 16-epiestriol may be studied for its potential therapeutic applications, particularly in hormone replacement therapies and in understanding estrogen-related conditions. However, as with all hormones, its effects can vary based on dosage and individual biological responses.
Formula:C18H24O3
InChI:InChI=1/C18H24O3/c1-18-7-6-13-12-5-3-11(19)8-10(12)2-4-14(13)15(18)9-16(20)17(18)21/h3,5,8,13-17,19-21H,2,4,6-7,9H2,1H3/t13-,14-,15+,16+,17+,18+/m1/s1
InChI key:InChIKey=PROQIPRRNZUXQM-ZMSHIADSSA-N
SMILES:C[C@@]12[C@]([C@]3([C@@](C=4C(CC3)=CC(O)=CC4)(CC1)[H])[H])(C[C@H](O)[C@@H]2O)[H]
Synonyms:- (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
- 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
- 16-Epiestriol
- Estriol IMpurity F
- 1,3,5(10)-ESTRATRIEN-3,16B,17B-TRIOL
- 16β-Oestriol
- Estra-1,3,5(10)-triene-3,16beta,17beta-triol
- EPIESTRIOL, 16-
- 16-EPISTRIOL
- 16beta,17beta-Estriol
- 1,3,5[10]-ESTRATRIENE-3,16BETA,17BETA-TRIOL
- EPIESTRIOL, 16-(RG)
- 16BETA-HYDROXY-17BETA-ESTRADIOL
- 16-epioestriol
- Estra-1,3,5(10)-triene-3,16,17-triol, (16beta,17beta)-
- (16,17)-Estra-1,3,5(10)-triene-3,16,17-triol
- 3,16beta,17beta-Estriol
- 16BETA-HYDROXYESTRADIOL
- (8R,9S,13S,14S,16S,17R)-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,16,17-triol
- 3,16BETA,17BETA-TRIHYDROXY-1,3,5[10]-ESTRATRIENE
- Conjugated Estrogens EP Impurity F
- 5(10)-triene-3,16,17-triol,(16beta,17beta)-estra-3
- 1,3,5(10)-ESTRATRIEN-3,16-BETA, 17-BETA-TRIOL
- See more synonyms
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Found 10 products.
Estriol EP Impurity F
CAS:Formula:C18H24O3Color and Shape:White To Off-White SolidMolecular weight:288.3916-Epiestriol
CAS:Formula:C18H24O3Purity:≥ 98.0%Color and Shape:White to off-white powderMolecular weight:288.38Estra-1,3,5(10)-triene-3,16β,17β-triol (16-epi-Estriol)
CAS:Controlled ProductFormula:C18H24O3Color and Shape:NeatMolecular weight:288.38Actriol
CAS:<p>Actriol (Epiestriol) is always used as Glucocorticoid Receptor agonist.</p>Formula:C18H24O3Purity:95.35% - 98.86%Color and Shape:SolidMolecular weight:288.3816-Epiestriol, Ultra Pure (contains less than 0.3% Estriol)
CAS:Controlled ProductFormula:C18H24O3Color and Shape:NeatMolecular weight:288.3816-Epiestriol
CAS:Controlled Product<p>Impurity Estriol EP Impurity F<br>Applications 16-Epiestriol (Estriol EP Impurity F) is a metabolite of Estradiol.<br>References Marrian, B., et al.: Biochem. J., 59, 136 (1955), Dietel, M., et al.: Cancer Res., 50, 6100 (1990), Schumacher, G., et al.: Clin. Cancer Res., 5, 493 (1999), Robert, J., et al.: J. Med. Chem., 46, 4805 (2003),<br></p>Formula:C18H24O3Color and Shape:WhiteMolecular weight:288.3816-Epiestriol
CAS:Controlled Product<p>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.</p>Formula:C18H24O3Purity:Min. 95%Color and Shape:PowderMolecular weight:288.38 g/mol









