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Saroglitazar Magnesium

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Catalog No. T12834Cas No. 1639792-20-3

Saroglitazar Magnesium is a novel peroxissome proliferator-activated receptor (PPAR) agonist with significant activation activity against PPARα (EC50 0.65pM) and moderate activation against PPARγ (EC50 3 nM).

Saroglitazar Magnesium

Saroglitazar Magnesium

🥰Excellent
Purity: 98.1%
Catalog No. T12834Cas No. 1639792-20-3
Saroglitazar Magnesium is a novel peroxissome proliferator-activated receptor (PPAR) agonist with significant activation activity against PPARα (EC50 0.65pM) and moderate activation against PPARγ (EC50 3 nM).
Pack SizePriceAvailabilityQuantity
1 mg$53In Stock
5 mg$139In Stock
10 mg$215In Stock
25 mg$343In Stock
50 mg$463In Stock
100 mg$592In Stock
200 mg$783In Stock
1 mL x 10 mM (in DMSO)$213In Stock
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Purity:98.1%
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Product Introduction

Bioactivity
Description
Saroglitazar Magnesium is a novel peroxissome proliferator-activated receptor (PPAR) agonist with significant activation activity against PPARα (EC50 0.65pM) and moderate activation against PPARγ (EC50 3 nM).
Targets&IC50
PPARγ:3 nM (EC50, HepG2 cell), PPARα:0.65 pM (EC50, HepG2 cell)
In vivo
In db/db mice, Saroglitazar (0.01-3 mg/kg per day, orally) treatment with 12-day causes dose-dependent reductions in serum triglycerides (TG), free fatty acids (FFA), and glucose. The ED50 for these effects is found to be 0.05, 0.19, and 0.19 mg/kg, respectively with highly significant (91%) reduction in serum insulin and AUC-glucose following oral glucose administration (59%) at 1 mg/kg dose.in Wistar rats and marmosets A 90-day repeated dose comparative study confirms efficacy (TG lowering) potential of Saroglitazar and has indicated low risk of PPAR-associated side effects in humans. Based on efficacy and safety profile, Saroglitazar appears to have good potential as novel therapeutic agent for treatment of dyslipidemia and diabetes[1].
Chemical Properties
Molecular Weight901.43
FormulaC50H56MgN2O8S2
Cas No.1639792-20-3
SmilesC(C)O1[Mg+2]2(O(CC)C(CC3=CC=C(OCCN4C(=CC=C4C)C5=CC=C(SC)C=C5)C=C3)C(=O)[O-]2)[O-]C(=O)C1CC6=CC=C(OCCN7C(=CC=C7C)C8=CC=C(SC)C=C8)C=C6
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 112.5 mg/mL (124.8 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.1093 mL5.5467 mL11.0935 mL55.4674 mL
5 mM0.2219 mL1.1093 mL2.2187 mL11.0935 mL
10 mM0.1109 mL0.5547 mL1.1093 mL5.5467 mL
20 mM0.0555 mL0.2773 mL0.5547 mL2.7734 mL
50 mM0.0222 mL0.1109 mL0.2219 mL1.1093 mL
100 mM0.0111 mL0.0555 mL0.1109 mL0.5547 mL

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