产品详情
T863 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.
In vitro | DMSO | 73 mg/mL (185.05 mM) | |
Water | Insoluble | ||
Ethanol | 1 mg/mL | ||
* <1 mg/ml means slightly soluble or insoluble. * Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
0.1 mM | 25.35 mL | 126.75 mL | 253.5 mL |
0.5 mM | 5.07 mL | 25.35 mL | 50.7 mL |
1 mM | 2.54 mL | 12.68 mL | 25.35 mL |
5 mM | 0.51 mL | 2.54 mL | 5.07 mL |
*The above data is based on the productmolecular weight 394.47. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
目录号 | A11386 |
---|---|
作用机制 | Inhibitor (抑制剂) |
M. Wt | 394.47 |
Formula | C22H26N4O3 |
Purity | >99% |
Storage | Store lyophilized at -20ºC, keep desiccated. |
CAS No. | 701232-20-4 |
Synonyms | T 863, T-863 |
SMILES | O=C(O)C[C@H]1CC[C@H](C2=CC=C(C3=NC4=C(N)N=CN=C4OC3(C)C)C=C2)CC1 |
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