BMS 687453

BMS 687453

CAT N°: 19404
Price:

From 49.00 41.65

BMS 687453 is a potent agonist of peroxisome proliferator-activated receptor ? (PPAR?; EC50 = 10 nM in a transactivation assay using HEK293 cells).{43668} It is selective for PPAR? over PPAR? (EC50 = 4,100 nM) as well as over a panel of human nuclear hormone receptors, including PPAR?, LXR, and RXR (EC50s = >25 ?M). BMS 687453 (10-100 mg/kg) reduces plasma triglyceride levels and increases HDL levels in human ApoA1 transgenic mice. It also reduces serum triglyceride and LDL levels in hamsters fed a high-fat diet.{31212}

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • N-[[3-[[2-(4-chlorophenyl)-5-methyl-4-oxazolyl]methoxy]phenyl]methyl]-N-(methoxycarbonyl)-glycine
  • Correlated keywords
    • BMS687453 p PPAR-? ? ? HEK-293 Apo-A1 A 1
  • Product Overview:
    BMS 687453 is a potent agonist of peroxisome proliferator-activated receptor ? (PPAR?; EC50 = 10 nM in a transactivation assay using HEK293 cells).{43668} It is selective for PPAR? over PPAR? (EC50 = 4,100 nM) as well as over a panel of human nuclear hormone receptors, including PPAR?, LXR, and RXR (EC50s = >25 ?M). BMS 687453 (10-100 mg/kg) reduces plasma triglyceride levels and increases HDL levels in human ApoA1 transgenic mice. It also reduces serum triglyceride and LDL levels in hamsters fed a high-fat diet.{31212}

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