ML-210
目录号: PL01010 纯度: ≥99%
CAS No. :1360705-96-9
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中文名称
ML-210
英文名称
ML-210
英文别名
CID 49766530;ML-210;[4-[Bis(4-chlorophenyl)methyl]piperazin-1-yl]-(5-methyl-4-nitro-1,2-oxazol-3-yl)methanone;ML 210;ML210;(4-(bis(4-chlorophenyl)methyl)piperazin-1-yl)(5-methyl-4-nitroisoxazol-3-yl)methanone;BRD7528;[4-[bis(4-chlorophenyl)methyl]-1-piperazinyl]-(5-methyl-4-nitro-3-isoxazolyl)methanone;TL_HRAS26;MLS003265661;HMS3874L03;BCP29439;SMR001941104;BDBM50547193;BM170835;ML 210, >=98% (HPLC);S0788;D83838
Cas No.
1360705-96-9
分子式
C22H20Cl2N4O4
分子量
475.32
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
ML-210 是一种选择性,共价的谷胱甘肽过氧化物酶 4 (GPX4) 抑制剂,EC50 为 30 nM。ML-210 结合 GPX4 硒代半胱氨酸残基。ML210 具有抗癌活性。
生物活性
ML-210 is a selective and covalent glutathione peroxidase 4 (GPX4) inhibitor with an EC 50 of 30 nM. ML-210 binds the GPX4 selenocysteine residue. ML-210 has anti-cancer activity.
性状
Solid
IC50 & Target[1][2]
Glutathione Peroxidase 4 (GPX4)
体外研究(In Vitro)
ML-210 exhibits cell-killing activity across a panel of 821 cancer cell lines (WM88, LOX-IMVI, CJM, U257, CAKI2, A498, HT1080, MC38, PANC02). ML-210 is a prodrug that requires cellular activation to bind GPX4.
ML-210 has IC50s of 71 nM, 272 nM and 107nM for BJeLR (HRASV12), BJeH-LT (without HRASV12) and DRD cell lines, respectively. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. John K. Eaton, et al. Targeting a Therapy-Resistant Cancer Cell State Using Masked Electrophiles as GPX4 Inhibitors. Biorxiv. 2018.
[2]. We?wer M, et al. Development of small-molecule probes that selectively kill cells induced to express mutant RAS. Bioorg Med Chem Lett. 2012 Feb 15;22(4):1822-6.
溶解度数据
In Vitro: DMSO : 25 mg/mL (52.60 mM; Need ultrasonic)配制储备液
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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