Orlistat

CAS No. 96829-58-2

Orlistat( Tetrahydrolipstatin )

Catalog No. M16871 CAS No. 96829-58-2

Orlistat is a drug designed to treat obesity. Its primary function is preventing the absorption of fats from the human diet, thereby reducing caloric intake.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
100MG 47 In Stock
200MG 73 In Stock
500MG 120 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Orlistat
  • Note
    Research use only, not for human use.
  • Brief Description
    Orlistat is a drug designed to treat obesity. Its primary function is preventing the absorption of fats from the human diet, thereby reducing caloric intake.
  • Description
    Orlistat is a drug designed to treat obesity. Its primary function is preventing the absorption of fats from the human diet, thereby reducing caloric intake. Orlistat works by inhibiting pancreatic lipase, an enzyme that breaks down triglycerides in the intestine. Without this enzyme, triglycerides from the diet are prevented from being hydrolyzed into absorbable free fatty acids and are excreted undigested.
  • In Vitro
    :Western Blot Analysis Cell Line:The human melanoma cell line M10,?Peripheral blood mononuclear cells?, The human Jurkat CD4+?T cell leukemia cell line, the human promyelocytic leukemia cell line HL-60,?the epithelial colon cancer HCT116 cells,non adherent mononuclear cells (NAMNC)Concentration:2.5, 5, 10, 20, 40 μM for Jurkat cells; 20 and 40 μM for HCT116 cells; 40 μM for normal NAMNC,? M10 melanoma, HL-60 promyelocytic leukemia, and HT-29 colon cancer cells Incubation Time:2 days for Jurkat cells; 2 or 4 days for HCT116 cells; 2 days for NAMNC, M10 melanoma, HL-60 promyelocytic leukemia, HT-29 colon cancer Result:Reduced by >50% the MGMT level at the concentration of 40 μM for Jurkat cells, whereas little or no effect was found when lower concentrations were used. Downregulation of MGMT expression is produced at 40 μM for HCT116 cells.Provoked an ~50% reduction of MGMT level at 40 μM in normal NAMNC, and HL-60 promyelocytic leukemia, HT-29 colon cancer cells except for melanoma M10 cells that showed no downregulation of the protein.
  • In Vivo
    Animal Model:Eighteen male rats of Sprague–Dawley strain aged between 8–10 weeks weighing 200-250 g Dosage:10 mg/kg/day?.Administration:Orally; six weeksResult:Treatment persistently restored the increased body weight, which was significantly observed at the ninth week until the end of the experimental period.?
  • Synonyms
    Tetrahydrolipstatin
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    Fatty Acid Synthase
  • Recptor
    FAS| triacylglycerol lipase
  • Research Area
    Metabolic Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    96829-58-2
  • Formula Weight
    495.73
  • Molecular Formula
    C29H53NO5
  • Purity
    >98% (HPLC)
  • Solubility
    Ethanol: 99 mg/mL (199.7 mM); DMSO: 99 mg/mL (199.7 mM)
  • SMILES
    CC(C)C[C@H](NC=O)C(O[C@@H](CCCCCCCCCCC)C[C@@H]([C@@H]1CCCCCC)OC1=O)=O
  • Chemical Name
    [(2S)-1-[(2S,3S)-3-hexyl-4-oxooxetan-2-yl]tridecan-2-yl] (2S)-2-formamido-4-methylpentanoate

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Uusitupa M. Curr Opin Lipidol. 1999 Feb;10(1):3-7.
molnova catalog
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