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 |
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| 200MG | 73 | In Stock |
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| 500MG | 120 | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameOrlistat
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NoteResearch use only, not for human use.
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Brief DescriptionOrlistat is a drug designed to treat obesity. Its primary function is preventing the absorption of fats from the human diet, thereby reducing caloric intake.
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DescriptionOrlistat 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.
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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.
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In VivoAnimal 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.?
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SynonymsTetrahydrolipstatin
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PathwayMetabolic Enzyme/Protease
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TargetFatty Acid Synthase
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RecptorFAS| triacylglycerol lipase
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Research AreaMetabolic Disease
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Indication——
Chemical Information
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CAS Number96829-58-2
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Formula Weight495.73
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Molecular FormulaC29H53NO5
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Purity>98% (HPLC)
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SolubilityEthanol: 99 mg/mL (199.7 mM); DMSO: 99 mg/mL (199.7 mM)
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SMILESCC(C)C[C@H](NC=O)C(O[C@@H](CCCCCCCCCCC)C[C@@H]([C@@H]1CCCCCC)OC1=O)=O
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Chemical Name[(2S)-1-[(2S,3S)-3-hexyl-4-oxooxetan-2-yl]tridecan-2-yl] (2S)-2-formamido-4-methylpentanoate
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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ACSS2-IN-2
ACSS2-IN-2 is an inhibitor of acyl-CoA synthetase short-chain family member 2 (ACSS2). ACSS2-IN-2 can inhibit ACSS2 activity with an IC50 value of 3.8 nM. ACSS2-IN-2 can be used for the research of several diseases, such as viral infection, metabolic disorders, neuropsychiatric diseases, inflammatory/autoimmune conditions and cancer.
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FASN-IN-2
FASN-IN-2 is a Fatty Acid Synthase (FASN) inhibitor(IC50 of 0.052 μM and an EC50 of 0.072 μM),with potential antineoplastic activity.?TVB-2640 is an orally bioavailable fatty acid synthase (FASN) inhibitor, with potential antineoplastic activity.
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