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 |
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