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|---|---|---|
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| Cat. No. : | HY-122746 |
| M.Wt: | 404.55 |
| Formula: | C21H36N6O2 |
| Purity: | >98 % |
| Solubility: | 10 mM in DMSO |
E67-2, as the E67 derivative, is a low-toxicity, selective KIAA1718 Jumonji domain inhibitor with an IC50 value of 3.4 µM. E67-2 selectively inhibits histone H3 lysine 9 (H3K9) Jumonji demethylase as well as histone H3 lysine 4 (H3K4) demethylase[1]. IC50 & Target: IC50: 3.4 μM (H3K9 Jumonji demethylase)[1] In Vitro: E67-2 (1~100 μM; 5 minutes) reduces inhibitory effect against GLP by a factor of approximately 1500, resulting in an IC50 of 75 µM. E67-2 has much reduced inhibition on PHF8 on the doubly methylated H3(1-24)K4me3K9me2 peptide substrate. E67-2 (100~100000 nM; 24 hours; fibroblasts) has significantly reduced cell toxicity [1].
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