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SPR inhibitor 3 is an effective sepiapterin reductase inhibitor. SPR inhibitor 3 decreases neuropathic and inflammatory pain through a reduction of BH4 levels. SPR inhibitor 3 shows a high binding affinity to human SPR in a cell-free assay (IC50=74 nM) and efficiently reduces biopterin levels in a cell-based assay (IC50=5.2 μM).
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SPR inhibitor 3 is an effective sepiapterin reductase inhibitor. SPR inhibitor 3 decreases neuropathic and inflammatory pain through a reduction of BH4 levels. SPR inhibitor 3 shows a high binding affinity to human SPR in a cell-free assay (IC50=74 nM) and efficiently reduces biopterin levels in a cell-based assay (IC50=5.2 μM).
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
2 mg | ¥ 642 | 5日内发货 | |
5 mg | ¥ 1,080 | 5日内发货 | |
10 mg | ¥ 1,530 | 5日内发货 | |
25 mg | ¥ 3,150 | 5日内发货 | |
50 mg | ¥ 6,220 | 5日内发货 | |
1 mL x 10 mM (in DMSO) | ¥ 1,180 | 5日内发货 |
产品描述 | SPR inhibitor 3 is an effective sepiapterin reductase inhibitor. SPR inhibitor 3 decreases neuropathic and inflammatory pain through a reduction of BH4 levels. SPR inhibitor 3 shows a high binding affinity to human SPR in a cell-free assay (IC50=74 nM) and efficiently reduces biopterin levels in a cell-based assay (IC50=5.2 μM). |
靶点活性 | Sepiapterin reductase:74 nM |
体外活性 | SPR inhibitor 3 obviously decreases SPR activity in mouse primary cultures of sensory neurons (IC50=0.45 μM) without affecting the activity of the GTP cyclohydroxylase 1 enzyme [1]. |
别名 | SPRi3 |
分子量 | 262.3 |
分子式 | C14H18N2O3 |
CAS No. | 1292285-54-1 |
密度 | 1.241 g/cm3 (Predicted) |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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