Cas No.: | 1360705-96-9 |
Synonyms: | CID 49766530;ML-210;[4-[Bis(4-chlorophenyl)methyl]piperazin-1-yl]-(5-methyl-4-nitro-1,2-oxazol-3-yl)methanone |
SMILES: | ClC1=CC=C(C(N2CCN(C(C3=NOC(C)=C3[N+]([O-])=O)=O)CC2)C2=CC=C(Cl)C=C2)C=C1 |
Formula: | C22H20Cl2N4O4 |
M.Wt: | 475.32460308075 |
Purity: | >98% |
Sotrage: | 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO |
Description: | ML-210,the most potent compound in the nitroisoxazole series, is a selective covalent inhibitor of glutathione peroxidase 4 (GPX4) by binding the selenocysteine residue[1]. ML-210 has IC50s of 71 nM, 272 nM and 107nM for BJeLR (HRASV12), BJeH-LT (without HRASV12) and DRD cell lines, respectively[2]. |
Target: | Glutathione Peroxidase 4 (GPX4)[1] |
References: | [1]. John K. Eaton, et al. Targeting a Therapy-Resistant Cancer Cell State Using Masked Electrophiles as GPX4 Inhibitors. Biorxiv. 2018. [2]. Weïwer 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. |