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| Product | Description | |
|---|---|---|
| T863 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| T863 | T-863 is an orally active, selective and potent DGAT1 (Acyl-CoA:diacylglycerol acyltransferase 1) inhibitor that interacts with the acyl-CoA binding site of DGAT1, and inhibits triacylglycerol synthesis in cells. It causes weight loss, reduction in serum and liver triglycerides, and improved insulin sensitivity in obese mice. Synonyms: DGAT-1 inhibitor; DGAT 1 inhibitor; T863; T-863; T 863. Grades: >98%. CAS No. 701232-20-4. Molecular formula: C22H26N4O3. Mole weight: 394.47. |  |
| T863 | T863 is an orally active, selective and potent DGAT1 (acyl-CoA:diacylglycerol acyltransferase 1) inhibitor with an IC50 of 15 nM. T863 has no inhibitory activity against human MGAT3, human DGAT2, or human MGAT2. T863 interacts with the acyl-CoA binding site of DGAT1, and inhibits triacylglycerol synthesis in cells[1][2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 701232-20-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-32219. |  |
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