CAS NO: | 2421119-60-8 |
包装 | 价格(元) |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
生物活性 | JKE-1674 is an orally activeglutathione peroxidase4 (GPX4) inhibitor and an active metabolite ofGPX4inhibitor ML-210. JKE-1674, an analog of ML-210 in which the nitroisoxazole ring is replaced with an α-nitroketoxime. JKE-1674 can convert into a nitrile oxide JKE-1777. JKE-1674 kills LOX-IMVI cells in a manner that is equipotent to ML-210 and is completely rescued byferroptosisinhibitors[1][2][3]. | ||||||||||||||||
IC50& Target | GPX4[1] | ||||||||||||||||
体外研究 (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[1]. | ||||||||||||||||
体内研究 (In Vivo) | JKE-1674 (50 mg/kg; p.o.) can be detected in the serum of mice dosed orally with the compound[1].
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分子量 | 451.30 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C20H20Cl2N4O4 | ||||||||||||||||
CAS 号 | 2421119-60-8 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | 4°C, protect from light *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 100 mg/mL(221.58 mM;Need ultrasonic) 配制储备液
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以下溶剂前显示的百
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