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Z-WEHD-FMK is a cell-permeable and irreversible inhibitor of caspase-1/5. It also shows a robust inhibitory effect on cathepsin B activity (IC50: 6 μM).


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Z-WEHD-FMK is a cell-permeable and irreversible inhibitor of caspase-1/5. It also shows a robust inhibitory effect on cathepsin B activity (IC50: 6 μM).
| 规格 | 价格 | 库存 | 数量 | 
|---|---|---|---|
| 5 mg | ¥ 3,740  | 待询 | |
| 10 mg | ¥ 5,410  | 待询 | |
| 50 mg | ¥ 16,200  | 待询 | |
| 100 mg |  待询   | 待询 | |
| 200 mg |  待询   | 待询 | 
Z-WEHD-FMK 相关产品
| 产品描述 | Z-WEHD-FMK is a cell-permeable and irreversible inhibitor of caspase-1/5. It also shows a robust inhibitory effect on cathepsin B activity (IC50: 6 μM).  | 
| 体外活性 | Z-WEHD-FMK (80 μM; 9 hours) nearly completely blocks C. trachomatis-induced cleavage of golgin-84 and increases GM130 expression in cells [1]. Administered 30 minutes before exposure to E. piscicida, Z-WEHD-FMK effectively inhibits 0909I E. piscicida-induced ZF4 cell cytotoxicity and pyroptotic morphology [2]. Z-WEHD-FMK (20 μM; 18-24 hours following exposure to Cr3+, Ni2+, and Co2+) significantly reduces IL-1β release in bone marrow-derived macrophages by 76% to 86% with 200 to 400 ppm Cr3+, by 35% to 45% with 48 ppm or higher Ni2+, and below detection threshold with 6 ppm Co2+, as well as by 40% to 48% with 12 to 24 ppm Co2+ [3].  | 
| 分子量 | 763.78 | 
| 分子式 | C37H42FN7O10 | 
| CAS No. | 210345-00-9 | 
| 密度 | no data available | 
| 存储 | keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | 
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