ML-210 (Synonyms: DPI10) |
| رقم الكتالوجGC18705 |
ML-210 هو مثبط انتقائي وتساهمي للجلوتاثيون بيروكسيديز 4 (GPX4) مع EC50 من 30 نانومتريربط ML-210 بقايا GPX4 selenocysteineML-210 له نشاط مضاد للسرطان
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Cas No.: 1360705-96-9
Sample solution is provided at 25 µL, 10mM.
ML-210 is an inhibitor of glutathione peroxidase 4 (GPX4).[1] It reduces viability of mesenchymal-state KP4 cells, an effect that can be blocked by the arachidonic acid lipoxygenase inhibitors PD 146176 and zileuton. It is also selectively lethal to mutant RAS oncogene-expressing cells (IC50s = 71 and 272 nM in HRASG12V-expressing and wild-type RAS-expressing BJeH cells, respectively).[2]
Reference:
[1]. Viswanathan, V.S., Ryan, M.J., Dhruv, H.D., et al. Dependency of a therapy-resistant state of cancer cells on a lipid peroxidase pathway. Nature 547(7664), 453-457 (2017).
[2]. Weïwer, M., Bittker, J.A., Lewis, T.A., et al. Development of small-molecule probes that selectively kill cells induced to express mutant RAS. Bioorg. Med. Chem. Lett. 22(4), 1822-1826 (2012).
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