Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Cevoglitazar (LBM-642) is a PPARɑ agonist and PPARγ agonist. Cevoglitazar potently reduces food intake and body weight in obese mice and cynomolgus monkeys.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
1 mg | In stock | $ 108.00 | |
5 mg | In stock | $ 260.00 | |
10 mg | In stock | $ 390.00 | |
25 mg | In stock | $ 653.00 | |
50 mg | In stock | $ 928.00 | |
100 mg | In stock | $ 1,260.00 | |
500 mg | In stock | $ 2,530.00 |
Description | Cevoglitazar (LBM-642) is a PPARɑ agonist and PPARγ agonist. Cevoglitazar potently reduces food intake and body weight in obese mice and cynomolgus monkeys. |
In vivo |
Cevoglitazar (0.5 mg/kg; 7 d) plasma levels of glucose and insulin were normalized.[1] Cevoglitazar (50 and 500 mg/kg; obese and insulin-resistant cynomolgus monkeys; 4 weeks) lowered food intake and body weight in a dose-dependent manner. In these animals, cevoglitazar also reduced fasting plasma insulin and, at the highest dose, reduced hemoglobin A1c levels by 0.4%.[1] Cevoglitazar (5 mg/kg) reduced BW gain and adiposity, independent of food intake. In the muscle, cevoglitazar improves the lipid profile via both PPARalpha- and PPARgamma-mediated mechanisms, and cevoglitazar reduced hepatic lipid concentration below baseline levels (p < 0.05). Metabolic profiling showed that in the liver, cevoglitazar functions largely through PPARalpha agonism resulting in increased beta-oxidation. Cevoglitazar only induced small changes to the lipid composition of visceral fat.[2] |
Synonyms | LBM-642, LBM 642, LBM642 |
Molecular Weight | 558.53 |
Formula | C27H21F3N2O6S |
CAS No. | 839673-52-8 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
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Cevoglitazar 839673-52-8 DNA Damage/DNA Repair Metabolism PPAR LBM-642 LBM 642 LBM642 inhibitor inhibit