ESTRADIOL

Estradiol is the primary human estrogen regulating reproductive and bone health. Used in HRT. Side effects include breast tenderness, nausea, and thrombotic risk. Only GMP materials will be supplied, logistics all according to GDP.

SKU: 509e0f7d6c44 Category: Tag:

Product Description


Mechanism of Action

Estradiol (E2) is the primary endogenous estrogen, binding ER and ER to regulate transcription across reproductive, skeletal, cardiovascular and neural tissues. It modulates gene expression through nuclear receptor signalling and membraneinitiated steroid signalling.

Benefits and Advantages

Used in estrogenreceptor biology, endocrinesignalling research, bonemetabolism modelling, and reproductivephysiology assays.

Side Effects and Risks

Risks include thromboembolic events, breast tenderness, nausea, endometrial stimulation and fluid retention. Handle with hormonemodulator precautions.

Only GMP materials will be supplied, logistics all according to GDP.

Datasheet


Molecular Formula

C18H24O2

Molecular Weight

272.4 g/mol

CAS Number

50-28-2

Storage Condition

Do not store unpouched. Apply immediately upon removal from the protective pouch.

Solubility

Solubility depends on solvent and conditions (e.g., pH). Please contact us for solvent-specific guidance.

Purity

Purity information is available upon request (COA).

Synonym

estradiol; beta-Estradiol; 50-28-2; 17beta-Estradiol; Oestradiol

IUPAC/Chemical Name

(8R,9S,13S,14S,17S)-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,17-diol

InChl Key

VOXZDWNPVJITMN-ZBRFXRBCSA-N

InChl Code

InChI=1S/C18H24O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-17,19-20H,2,4,6-9H2,1H3/t14-,15-,16+,17+,18+/m1/s1

References

https://pubchem.ncbi.nlm.nih.gov/compound/5757;

3D Conformer.

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