CAS 18650-87-8

estriol 3-benzyl ether

Description:

Estriol 3-benzyl ether, with the CAS number 18650-87-8, is a synthetic derivative of estriol, a naturally occurring estrogen. This compound features a benzyl ether functional group, which enhances its lipophilicity and may influence its biological activity. Estriol itself is known for its relatively weak estrogenic activity compared to other estrogens like estradiol. The introduction of the benzyl group can modify the pharmacokinetics and receptor binding properties of the molecule. Typically, compounds like estriol 3-benzyl ether are studied for their potential applications in hormone replacement therapy and other therapeutic areas related to estrogen modulation. In terms of physical properties, it is likely to be a solid or liquid at room temperature, with solubility in organic solvents. Safety and handling precautions are essential, as with all chemical substances, due to potential biological effects. Further research is often required to fully elucidate its pharmacological profile and therapeutic potential.

Formula: C₂₅H₃₀O₃

Estriol 3-Benzyl Ether

CAS: 18650-87-8

Color and Shape: Neat

Ref: 86-MM0130.16

Estriol 3-Benzyl Ether

CAS: 18650-87-8

Formula: C₁₈H₂₂O₃

Color and Shape: White To Off-White Solid

Molecular weight: 378.52

Ref: 4Z-E-3518

3-O-Benzyl Estriol

Controlled Product

CAS: 18650-87-8

Applications Protected Estriol.
References Gohil, V., et al.: Nat. Biotechnol., 28, 249 (2010),

Formula: C₂₅H₃₀O₃

Color and Shape: Neat

Molecular weight: 378.50

Ref: TR-B276500

3-O-Benzyl Estriol-d1

Controlled Product

CAS: 18650-87-8

Applications Protected Estriol.
References Gohil, V., et al.: Nat. Biotechnol., 28, 249 (2010),

Formula: C₂₅DH₂₉O₃

Color and Shape: Neat

Molecular weight: 379.51

Ref: TR-B276502

3-O-Benzyl estriol

Controlled Product

CAS: 18650-87-8

3-O-Benzyl estriol is a synthetic estrogen that is used to treat menopausal symptoms. This drug has been shown to have a high affinity for the estrogen receptor, and it is also able to activate the estrogen receptor in cells. 3-O-Benzyl estriol has been shown to be more potent than other estrogens such as estrone or estriol and has been shown to increase the synthesis of proteins by increasing RNA synthesis. 3-O-Benzyl estriol is conjugated with glucuronic acid and excreted in the bile. It also has a number of metabolic transformations, including pyrolysis, which produces cyanamid and triethylamine.

Formula: C₂₅H₃₀O₃

Purity: Min. 95%

Molecular weight: 378.5 g/mol

Ref: 3D-FB18292

3-O-Benzyl Estriol

CAS: 18650-87-8

Formula: C₁₈H₂₂O₃

Molecular weight: 378.5

Ref: ST-EA-CP-E28012