ESTROPIPATE

Estropipate is an estrogen compound used for menopausal symptoms and bone loss prevention. Side effects include fluid retention, headache, and clot risk. Only GMP materials will be supplied, logistics all according to GDP.

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Product Description


Mechanism of Action

Estropipate is a stabilized form of estrone in which estrone is complexed with piperazine sulfate to improve oral stability and absorption. After administration, the complex dissociates to release free estrone, which is converted intracellularly into estradiol and activates ER and ER. Through estrogenreceptor signalling, it regulates gene transcription in reproductive, skeletal, vascular and metabolic tissues.

Benefits and Advantages

Used in estrogenreplacement modelling, ERactivation assays, endocrineaxis research, bonemetabolism studies and hormonepharmacokinetics investigations.

Side Effects and Risks

Risks include thromboembolism, nausea, breast tenderness, fluid retention and hepatic stimulation. Handle with estrogencomplex precautions.

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

Datasheet


Molecular Formula

C23H30O6

Molecular Weight

436.6 g/mol

CAS Number

7280-37-7

Storage Condition

Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light.

Solubility

less than 1 mg/mL at 70 °F (NTP, 1992)

Purity

Purity information is available upon request (COA).

Synonym

Estropipate; 7280-37-7; Piperazine estrone sulfate; Ogen; Sulestrex

IUPAC/Chemical Name

[(8R,9S,13S,14S)-13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl] hydrogen sulfate;piperazine

InChl Key

HZEQBCVBILBTEP-ZFINNJDLSA-N

InChl Code

InChI=1S/C18H22O5S.C4H10N2/c1-18-9-8-14-13-5-3-12(23-24(20,21)22)10-11(13)2-4-15(14)16(18)6-7-17(18)19;1-2-6-4-3-5-1/h3,5,10,14-16H,2,4,6-9H2,1H3,(H,20,21,22);5-6H,1-4H2/t14-,15-,16+,18+;/m1./s1

References

https://pubchem.ncbi.nlm.nih.gov/compound/5284555;

3D Conformer.

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