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Heathy Anti Estrogen Steroids Misoprostol For Muscle Gain CAS 59122-46-2

Heathy Anti Estrogen Steroids Misoprostol For Muscle Gain CAS 59122-46-2

  • Heathy Anti Estrogen Steroids Misoprostol For Muscle Gain CAS 59122-46-2
  • Heathy Anti Estrogen Steroids Misoprostol For Muscle Gain CAS 59122-46-2
  • Heathy Anti Estrogen Steroids Misoprostol For Muscle Gain CAS 59122-46-2
  • Heathy Anti Estrogen Steroids Misoprostol For Muscle Gain CAS 59122-46-2
Heathy Anti Estrogen Steroids Misoprostol For Muscle Gain CAS 59122-46-2
Product Details:
Place of Origin: Hubei, China
Brand Name: Bodybiological
Certification: ISO9001, SGS
Model Number: CAS: 59122-46-2
Payment & Shipping Terms:
Minimum Order Quantity: 10gram
Price: USD1/gram
Packaging Details: Foil bag
Delivery Time: Within 24 hours
Payment Terms: T/T, Western Union, MoneyGram
Supply Ability: 120kg/month
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Detailed Product Description
Keywords: Misoprostol CAS: 59122-46-2
Appearance: White Powder Shipping Method: Fedex, TNT, DHL, UPS, HK EMS
Payment Terms: Money Gram, Western Union, Bank Transfer MOQ: 10gram
Purity: 99.8% Policy: Reshipping Policy
Export Market: USA, UK, Brazil, Thailand, Canada Brand: Bodybiological
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Heathy Anti Estrogen Steroids Misoprostol for Muscle Gain CAS 59122-46-2

 

Basic information:

 

Name:Misoprostol
Synonyms: CYTOTEC;9-OXO-11ALPHA,16-DIHYDROXY-16-METHYL-PROST-13E-EN-1-OIC ACID;9-OXO-11ALPHA,16-DIHYDROXY-16-METHYL-PROST-13E-EN-1-OIC ACID, METHYL ESTER;(11A,13E)-(-)-11,16-DIHYDROXY-16-METHYL-9-OXO-PROST-13-EN-1-OIC ACID METHYL ESTER;(11alpha,13e)-(+)-11alpha,16-dihydroxy-16-methyl-9-oxoprost-13e-en-1-oic acid methyl ester
CAS: 59122-46-2
MF: C22H38O5
MW: 382.54
Product Categories:Prostaglandins;Pharmaceuticals;Prostanoid receptor and related
Chemical Properties: White Solid
Assay:99%
Packing 10g/foil bag or as required

 

Detailed information:
 

A cell-permeable synthetic steroid that acts as a potent antagonist of progesterone and glucocorticoid receptors. Inhibits P-glycoprotein (P-gp) function and down-modulates P-gp mediated drug resistance. Displays anti-angiogenic effects and suppresses vascular endothelial growth factor (VEGF) production. Regulates the expression of Fas and FasL in mouse endometrium and TRAIL in prostate cancer cells. As an antioxidant, it offers neuroprotection against controlled cortical impact (CCI) in CA1 pyramidal cells, as well as Aβ-, H2O2-, and glutamate-induced injury to mouse hippocampal HT22 cells.

 

Applications:

 

The discovery of the first competitive progesterone antagonist, Mifepristone, has stimulated an intense search for more potent and more selective antiprogestins[1]. Cell growth is evaluated after 4 days of exposure to Mifepristone at 10 μM, a concentration close to the plasma concentration achievable in humans. The antiproliferative effect of Cisplatin is potentiated when administered in combination with Mifepristone in HeLa cells. The IC50 of Cisplatin in combination with Mifepristone is lower (14.2 μM) than that of Cisplatin alone (34.2 μM) in HeLa cells with an approximately 2.5-fold difference. After treatment with Mifepristone, the accumulation of intracellular Cisplatin in HeLa cells is 2-fold greater, representing a significant difference (p=0.009), compare with Cisplatin alone from 0.79 to 1.52 μg/mg of protein.

 

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