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Saroglitazar Magnesium

رقم الكتالوجGC31325

المغنيسيوم Saroglitazar هو ناهض جديد لمستقبلات البيروكسيسوم المنشط (PPAR) مع PPARα السائد ونشاط PPARγ المعتدل بقيم EC50 تبلغ 0.65 ميكرومتر و 3 نانومتر في خلايا HepG2 ، على التوالي

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Saroglitazar Magnesium التركيب الكيميائي

Cas No.: 1639792-20-3

الحجم السعر المخزون الكميّة
10mM (in 1mL DMSO)
547٫00
متوفر
1mg
138٫00
متوفر
5mg
358٫00
متوفر
10mg
552٫00
متوفر
25mg
1103٫00
متوفر
50mg
1655٫00
متوفر

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Sample solution is provided at 25 µL, 10mM.

Description Protocol Chemical Properties Product Documents Related Products

Saroglitazar magnesium is a novel peroxisome proliferator-activated receptor (PPAR) agonist with predominant PPARα and moderate PPARγ activity with EC50 values of 0.65 pM and 3 nM in HepG2 cells, respectively.

In db/db mice, 12-day treatment with Saroglitazar (0.01-3 mg/kg per day, orally) 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. A 90-day repeated dose comparative study in Wistar rats and marmosets 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].

[1]. Jain MR, et al. Saroglitazar, a novel PPARα/γ agonist with predominant PPARα activity, shows lipid-lowering and insulin-sensitizing effects in preclinical models. Pharmacol Res Perspect. 2015 Jun;3(3):e00136.

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