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925891-74-3

925891-74-3 Structure

925891-74-3 Structure
IdentificationBack Directory
[Name]

N-Octadecyl-N'-propyl-sulfamide
[CAS]

925891-74-3
[Synonyms]

N-Octadecyl-N'-propyl-sulfamide
Sulfamide, N-octadecyl-N'-propyl-
N-(propylsulfamoyl)octadecan-1-amine
[Molecular Formula]

C21H46N2O2S
[MDL Number]

MFCD10565622
[MOL File]

925891-74-3.mol
[Molecular Weight]

390.67
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

≤0.2mg/ml in ethanol
[form ]

crystalline solid
Hazard InformationBack Directory
[Description]

Peroxisome proliferator-activated receptors (PPARs) play an essential role in regulating lipid and glucose metabolism. Oleoyl ethanolamide (OEA), a natural ligand for PPARα, has been shown to suppress food intake and reduce weight gain in rats when administered systemically at 10 mg/kg intraperitoneally. N-Octadecyl-N''-propyl-sulfamide is an analog of OEA with selective binding affinity for PPARα. It is a more potent activator of PPARα, exhibiting an EC50 value of 100 nM, compared to OEA, which exhibits an EC50 value of 120 nM. At a dose of 1 mg/kg for 8-11 days, N-octadecyl-N''-propyl-sulfamide induces satiety, thereby decreasing food-intake, body weight, and plasma triglyceride concentration in free-feeding Wistar and obese Zucker (fa/fa) rats.
[Uses]

Peroxisome proliferator-activated receptors (PPARs) play an important role in regulating lipid and glucose metabolism, and oleoylethanolamide (OEA) is a natural ligand for PPARα. N-Octadecyl-N'-propyl-sulfamide is an analog of OEA and a potent activator of PPARα, with selective binding affinity for PPARα (EC50=100 nM, compared to 120 nM for OEA). N-Octadecyl-N'-propyl-sulfamide (10 mg/kg; ip) inhibits food intake and reduces body weight gain in rats. At a dose of 1 mg/kg, N-Octadecyl-N'-propyl-sulfamide induces satiety, thereby reducing food intake, body weight, and plasma triglyceride concentrations in free-feeding Wistar rats and obese Zucker (fa/fa) rats.
[IC 50]

PPARα
[storage]

Store at -20°C
[References]

[1]. cano c, pavón j, serrano a, et al. novel sulfamide analogs of oleoylethanolamide showing in vivo satiety inducing actions and pparalpha activation. j med chem. 2007 jan 25;50(2):389-93.
[2]. fu j1, gaetani s, oveisi f, et al. oleylethanolamide regulates feeding and body weight through activation of the nuclear receptor ppar-alpha. nature. 2003 sep 4;425(6953):90-3.
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