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| Synonyms: | Raloxifene | CAS No: | 82640-04-8 |
|---|---|---|---|
| Molecular Formula: | C28H29NO4S | Molecular Weight: | 475.5992 |
| Appearance: | Light Yellow Crystalline Powder | Standard: | Enterprise Standard |
| Packing: | As Per Your Requirements | Application: | Pharmaceutical Intermediate |
| Assay: | 99% | Price: | Negotiable |
| Packaging Details: | Very Discreet. As Required. | Payment Terms: | T/T, , |
| High Light: | strongest anabolic steroid,testosterone based steroid |
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PharmaceuticalPowder Raloxifene Hydrochloride Raw Material Anti-estrogen
| commerce clause | |
| Minimum order quantity | 10gram for powder Products ; 100ml usually for oil products for quality testing |
| Supply Ability | mass stock |
| Packaging Details | Discreet25kg/plastic foil or tin bag or as required |
| Lead time | Within 12 hours,upon receipt of your payment cleared |
| Delivery time | Withing 5 working days after the payment cleared ,normally 6 days by air; 15 days by ship |
| Shipping | below 25kg by express, between 25kg~200kg by air, over 200kg by sea |
| Payment Terms | , , T/T, PayPal, Bank Transfer |
| Price | Negotiable |
| Remarks | Good receipt will be according to time in different countries by means of Air shipment and EXPRESS. |
Raloxifene hydrochloride
Product name: Raloxifene hydrochloride
Synonyms: Keoxifene
Purity: 99%
CAS No.:82640-04-8
M.F.: C28H29NO4S
M.W.: 475.5992
Appearance: light yellow crystalline powder,
USES: Raloxifene will be like tamoxifen as effective,
and less adverse effects.
Usage:
1. Amino acid, nutrient
2. Labeled Raloxifene, intended for use as an internal standard for the quantification by GC- or LC-mass
spectrometry.
3. A nonsteroidal, selective estrogen receptor modulator (SERM). Antiosteoporotic.
Description:
Raloxifene hydrochloride is a second-generation Selective Estrogen Receptor Modulator (SERM) of the benzothiophene family. This drug is similar in effect to tamoxifen, exhibiting estrogen receptor antagonist (blocking) properties in some tissues while acting as an estrogen receptor agonist (activator) in others.
The main point of variation between these two agents is their tissue selectivity. While raloxifene hydrochloride is a strong anti-estrogen in breast and uterine tissues, it appears to be estrogenic in bone. This allows it to protect bone density, mimicking the beneficial effects of endogenous estradiol. This is quite different from tamoxifen, which is anti-estrogenic in both breast and bone.
In a role that was novel for an anti-estrogen, raloxifene hydrochloride was approved by the FDA for the prevention and treatment of osteoporosis in post-menopausal women. It is also being investigated for several other potential uses, including the treatment and prevention of cardiovascular disease, breast cancer, gynecomastia, prostate cancer, acromegaly, and uterine cancer.
Raloxifene hydrochloride Mechanism of Action:
Evista (raloxifene hydrochloride) is an estrogen agonist/antagonist, referred to as a selective estrogen receptor modulator (SERM) and belongs to the benzothiophene class of compounds. The biological actions of raloxifene are largely mediated through binding to estrogen receptors.
This binding results in activation of estrogenic pathways in some tissues (agonism) and and the blockade of estrogenic pathways in other tissues (antagonism). The agonistic or antagonistic activity of raloxiffene depends on the extent of recruitment of coactivators and corepressors to estrogen receptor (ER) target gene promotors.
Raloxifene appears to act as an estrogen agonist in bone. It decreases bone resorption and bone turnover, increases bone mineral density and decreases fracture incidence.
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