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353280-43-0

353280-43-0 Structure

353280-43-0 Structure
IdentificationBack Directory
[Name]

[[4-[2-(6-Benzoyl-2-oxo-3(2H)-benzothiazolyl)ethoxy]phenyl]methyl]-1,3-propanedioicaciddimethylester
[CAS]

353280-43-0
[Synonyms]

S26948
S26948,S-26948
S 26948 >=98% (HPLC)
[[4-[2-(6-Benzoyl-2-oxo-3(2H)-benzothiazolyl)ethoxy]phenyl]methyl]-1,3-propanedioicaciddimethylester
2-[[4-[2-(6-Benzoyl-2-oxo-3(2H)-benzothiazolyl)ethoxy]phenyl]methyl]-propanedioic acid 1,3-dimethyl ester
Propanedioic acid, 2-[[4-[2-(6-benzoyl-2-oxo-3(2H)-benzothiazolyl)ethoxy]phenyl]methyl]-, 1,3-dimethyl ester
[Molecular Formula]

C28H25NO7S
[MDL Number]

MFCD18086885
[MOL File]

353280-43-0.mol
[Molecular Weight]

519.57
Chemical PropertiesBack Directory
[Melting point ]

65-67 °C(Solv: methanol (67-56-1))
[Boiling point ]

687.3±65.0 °C(Predicted)
[density ]

1.312±0.06 g/cm3(Predicted)
[storage temp. ]

Store at RT
[solubility ]

DMSO: soluble10mg/mL (clear solution)
[form ]

powder
[pka]

12.48±0.59(Predicted)
[color ]

white to beige
Safety DataBack Directory
[WGK Germany ]

3
Hazard InformationBack Directory
[Description]

S26948 is a peroxisome proliferator-activated receptor γ (PPARγ) agonist (EC50 = 8.83 nM in a transactivation assay). It is selective for PPARγ over PPARα, PPARβ/δ, and retinoid X receptor α (RXRα) at 10 μM. S26948 (30 mg/kg per day) decreases serum levels of glucose, triglycerides, non-esterified fatty acids, and insulin and increases hepatic palmitate oxidation in an ob/ob mouse model of type 2 diabetes. It decreases plasma levels of triglycerides and total and non-HDL cholesterol and the surface area of atherosclerotic lesions in the aortic sinus in an E2-KI transgenic mouse model of dyslipidemia and atherosclerosis fed a Western diet when administered at a dose of 30 mg/kg.
[Uses]

S26948 is a peroxisome proliferator-activated receptor γ modulator with potent antidiabetes and antiatherogenic effects.
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