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ML351 是一种高度特异的15-LOX-1抑制剂,其 IC50=200 nM。它对 T1D 非肥胖糖尿病小鼠模型的血糖异常和β细胞氧化应激有抑制作用。它对相关同工酶 (5-LOX、血小板 12-LOX、15-LOX-2、绵羊 COX-1 和人 COX-2) 表现出良好的选择性(>250倍)。


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ML351 是一种高度特异的15-LOX-1抑制剂,其 IC50=200 nM。它对 T1D 非肥胖糖尿病小鼠模型的血糖异常和β细胞氧化应激有抑制作用。它对相关同工酶 (5-LOX、血小板 12-LOX、15-LOX-2、绵羊 COX-1 和人 COX-2) 表现出良好的选择性(>250倍)。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 413 | In stock | |
| 5 mg | ¥ 993 | In stock | |
| 10 mg | ¥ 1,590 | In stock | |
| 25 mg | ¥ 2,880 | In stock | |
| 50 mg | ¥ 4,350 | In stock | |
| 100 mg | ¥ 5,970 | In stock | |
| 500 mg | ¥ 12,200 | In stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 1,090 | In stock |
ML351 相关产品
| 产品描述 | ML351 is a potent and selective inhibitor of human 15-lipoxygenase-1 (15 LOX)(IC50: 200 nM). |
| 靶点活性 | 15-LOX:200 nM |
| 体外活性 | ML351 exhibited nanomolar potency and excellent selectivity (>250-fold) versus 5-LOX, platelet 12-LOX, 15-LOX-2, ovine COX-1, and human COX-2. In mouse neuronal HT22 cells, ML351 dose-dependently protected against oxidative glutamate toxicity and completely reversed the increase in 12-HETE following glutamate treatment [2][3] |
| 分子量 | 249.27 |
| 分子式 | C15H11N3O |
| CAS No. | 847163-28-4 |
| Smiles | CNc1oc(nc1C#N)-c1cccc2ccccc12 |
| 密度 | 1.29 g/cm3 (Predicted) |
| 颜色 | White |
| 物理性状 | Solid |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||||||||||||
| 溶解度信息 | DMSO: 22.5 mg/mL (90.26 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||
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