CAS NO: | 210345-00-9 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
生物活性 | Z-WEHD-FMK is a potent, cell-permeable and irreversiblecaspase-1/5inhibitor. Z-WEHD-FMK also exhibits a robust inhibitory effect oncathepsin Bactivity (IC50=6 μM). Z-WEHD-FMK can be used to investigate cells for evidence ofapoptosis[1][2][4]. | ||||||||||||||||
IC50& Target[1][2] |
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体外研究 (In Vitro) | Z-WEHD-FMK (80 μM; 9 hours) elicits a near-complete blockage ofC. trachomatis-induced cleavage of golgin-84 and increases GM130 expression in cells[1].Z-WEHD-FMK (30 min before being exposed to E. piscicida) effectively inhibits 0909I E. piscicida induced ZF4 cells cytotoxicity and pyroptotic morphology. And in addition, it also inhibits the cytotoxicity induced by cytosolic LPS delivery[2].Z-WEHD-FMK (20 μM;18-24 hours following Cr3+,Ni2+, and Co2+) significantly induces a decrease of 76% to 86% in IL-1β release with 200 to 400 ppm Cr3+, it also induces a decrease of 35% to 45% with 48 ppm Ni2+or higher, Finally, this caspase-1 inhibitor induced a decrease with 6 ppm Co2+, down to a level below the detection threshold, and a decrease of 40% to 48% with 12 to 24 ppm Co2+in bone marrow-derived macrophages (BMDM)[3]. Western Blot Analysis[1]
Cell Viability Assay[2]
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分子量 | 763.77 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C37H42FN7O10 | ||||||||||||||||
CAS 号 | 210345-00-9 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | Sealed storage, away from moisture
*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 100 mg/mL(130.93 mM;Need ultrasonic) 配制储备液
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo: 请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
以下溶剂前显示的百
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