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Saroglitazar magnesium is a dual agonist of PPARalpha and PPARgamma (EC50s = 0.65 and 3,000 pM, respectively, in a transactivation assay in HepG2 cells). It decreases serum triglyceride, free fatty acid, and glucose levels in a db/db mouse model of diabetes when administered at doses ranging from 0.01 to 3 mg/kg per day for 12 days. It increases insulin sensitivity in an oral glucose challenge when administered at a dose of 1 mg/kg in db/db mice, as well as decreases LDL levels in hApoB100/hCETP mice and in hamsters fed a high-fat high-cholesterol diet. Saroglitazar magnesium (10 µM) reverses palmitic acid-induced decreases in the expression of mRNA encoding superoxide dismutase 1 (SOD1), SOD2, glutathione peroxidase (GPX), and catalase and increases in the expression of mRNA encoding TNF-alpha, IL-1beta, and IL-6 in HepG2 cells. It decreases hepatic inflammation and steatosis in a mouse model of non-alcoholic steatohepatitis (NASH) induced by a choline-deficient high-fat diet when administered at a dose of 3 mg/kg and inhibits hepatic fibrosis in a mouse model of fibrosis induced by carbon tetrachloride.Formal Name: (T-4)-bis[(alphaS)-alpha-(ethoxy-kappaO)-4-[2-[2-methyl-5-[4-(methylthio)phenyl]-1H-pyrrol-1-yl]ethoxy]benzenepropanoato-kappaO]-magnesium. CAS Number: 1639792-20-3. Molecular Formula: C50H56MgN2O8S2. Formula Weight: 901.4. Purity: >98%. Formulation: (Request formulation change), A solid. Solubility: DMSO: Sparingly soluble: 1-10 mg/ml. SMILES: CC1=CC=C(C2=CC=C(SC)C=C2)N1CCOC(C=C3)=CC=C3CC4[O]([Mg+2]([O-]C4=O)([O-]C5=O)[O](C5CC6=CC=C(OCCN7C(C8=CC=C(SC)C=C8)=CC=C7C)C=C6)CC)CC. InChi Code: InChI=1S/2C25H29NO4S.Mg/c2*1-4-29-24(25(27)28)17-19-6-10-21(11-7-19)30-16-15-26-18(2)5-14-23(26)20-8-12-22(31-3)13-9-20,/h2*5-14,24H,4,15-17H2,1-3H3,(H,27,28),/q,,+2/p-2. InChi Key: UJYFZCVPOSZDMK-UHFFFAOYSA-L.
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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