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4°C, protect from light
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货期:1-2天
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MedChemExpress LLC
- 规格:
10 mM * 1 mL/5 mg/10 mg/25 mg/50 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥1540.0 |
|---|---|---|---|
| 规格: | 5 mg | 产品价格: | ¥1400.0 |
| 规格: | 10 mg | 产品价格: | ¥2250.0 |
| 规格: | 25 mg | 产品价格: | ¥3800.0 |
| 规格: | 50 mg | 产品价格: | ¥5900.0 |
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JKE-1674
CAS No. : 2421119-60-8
MCE 国际站:JKE-1674
产品活性:JKE-1674 是一种具有口服活性的谷胱甘肽过氧化物酶 4 (GPX4) 抑制剂,是 GPX4 抑制剂 ML-210 的活性代谢物。JKE-1674 是 ML-210 的类似物,其中硝基异恶唑环被 α- 硝基酮肟取代。JKE-1674 可以转换成丁腈氧化物 JKE-1777。JKE-1674 以与 ML-210 相同的方式杀死 LOX-IMVI 细胞,并被 ferroptosis 抑制剂完全挽救。
研究领域:Metabolic Enzyme/Protease | Apoptosis
作用靶点:Glutathione Peroxidase | Ferroptosis
In Vitro: JKE-1674 exhibits activity indistinguishable from that of ML210 in cellular target engagement assays including yielding the same +434Da GPX4 adduct in cells. JKE-1674 kills LOX-IMVI cells in a manner that is equipotent to ML210 and is completely rescued by ferroptosis inhibitors. JKE-1674 forms a nitrile-oxide electrophile in cells. JKE-1674 dehydration yields a nitrile-oxide electrophile that binds GPX4. JKE-1674 exhibits far greater stability than chloroacetamide inhibitors.
In Vivo: JKE-1674 (50 mg/kg; p.o.) can be detected in the serum of mice dosed orally with the compound.
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