KDM5-C70 是一种 KDM5-C49 的乙酯衍生物，是一种有效的，细胞可渗透的泛 KDM5 组蛋白脱甲基酶抑制剂。KDM5-C70 在骨髓瘤细胞中具有抗增殖作用，从而导致 H3K4me3 水平在全基因组范围内升高。

KDM5-C70 is an ethyl ester derivative of KDM5-C49 and a potent, cell-permeable and pan-KDM5 histone demethylase inhibitor. KDM5-C70 has an antiproliferative effect in myeloma cells, leading to genome-wide elevation of H3K4me3 levels.

Oil

KDM5 histone demethylase

KDM5-C70 (10-10 M; 7 days; MM.1S myeloma cells) treatment shows antiproliferative effects after 7 days of treatment at elevated concentrations (estimated 50% reduction of viability/proliferation for KDM5-C70 at ~20 μM).
KDM5-C70 (50 μM; 7 days; MM.1S myeloma cells) treatment decreases the level of phosphorylation of retinoblastoma protein (Rb), while leaving the total level of phosphorylated Rb (pRb) unchanged, indicating impairment of cell cycle progression.
Chromatin immunoprecipitation followed by next-generation sequencing shows an increase in H3K4me3 levels around transcription start sites with KDM5-C70 but little change with GSK467A at 50 μM inhibitor concentrations. has not independently confirmed the accuracy of these methods. They are for reference only.

Room temperature in continental US; may vary elsewhere.

-20°C, stored under nitrogen In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)

[1]. Johansson C, et al. Structural analysis of human KDM5B guides histone demethylase inhibitor development. Nat Chem Biol. 2016 Jul;12(7):539-45.
[2]. Blair LP, et al. KDM5 lysine demethylases are involved in maintenance of 3UTR length. Sci Adv. 2016 Nov 18;2(11):e1501662.

In Vitro: DMSO : 100 mg/mL (297.24 mM; Need ultrasonic)配制储备液