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UGT1A1-IN-1 (化合物2) 为一种非竞争性UGT1A1抑制剂,具有5.02 μM的Ki值,有效阻断UGT1A1介导的1-O-葡糖苷酸化反应。此化合物能与UGT1A1在胆红素相同的配体结合位点上相结合。此外,UGT1A1-IN-1还可用作UGT1A1活性“开启”的荧光探针底物。
UGT1A1-IN-1 (化合物2) 为一种非竞争性UGT1A1抑制剂,具有5.02 μM的Ki值,有效阻断UGT1A1介导的1-O-葡糖苷酸化反应。此化合物能与UGT1A1在胆红素相同的配体结合位点上相结合。此外,UGT1A1-IN-1还可用作UGT1A1活性“开启”的荧光探针底物。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | 待询 | 10-14周 | |
50 mg | 待询 | 10-14周 |
产品描述 | UGT1A1-IN-1 (compound 2) acts as a non-competitive inhibitor of UGT1A1, effectively inhibiting the 1-O-glucuronidation process mediated by UGT1A1 with a Ki value of 5.02 μM. This compound binds to the same ligand-binding site on UGT1A1 as bilirubin and additionally functions as a 'turn-on' fluorescent probe substrate for UGT1A1 [1]. |
分子量 | 345.39 |
分子式 | C22H19NO3 |
CAS No. | 2097024-37-6 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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