Molecular Weight: | 600.02 |
Formula: | C28H38N6O2.3HCl |
Purity: | ≥98% |
CAS#: | 1392399-03-9 |
Solubility: | DMSO up to 100 mM |
Chemical Name: | N-(1-benzylpiperidin-4-yl)-6,7-dimethoxy-2-(4-methyl-1,4-diazepan-1-yl)quinazolin-4-amine trihydrochloride |
Storage: | Powder: 4oC 1 year. DMSO: 4oC 3 month; -20oC 1 year. |
Biological Activity:
BIX-01294 is a potent and selective G9a and GLP histone lysine methyltransferase inhibitor with an IC50 ~0.7 μM and 1.7 μM respectively. It has no activity at other histone methyltransferases. BIX-01294 modulates H3K9me2 levels in mammalian cells and potentiates induction of pluripotent stem cells from somatic cells in vitro. It could reactivate expression of HIV-1 from latently infected cells such as ACH-2 and OM10.1, suggesting the involvement of histone H3 lysine 9 (H3K9) methyltransferase G9a in the maintenance of HIV-1 latency. It can also inhibit malaria parasite histone methyltransferases, resulting in rapid and irreversible parasite death.
How to Use:
In vitro: BIX-01294 was used at 10 µM in vitro and cellular assays.
In vivo: n/a
Reference:
- 1. Kubicek S, et al. Reversal of H3K9me2 by a small-molecule inhibitor for the G9a histone methyltransferase. (2007) Mol Cell. 25(3):473-81.
- 2. Shi Y, et al. Induction of pluripotent stem cells from mouse embryonic fibroblasts by Oct4 and Klf4 with small-molecule compounds. (2008) Cell Stem Cell. 3(5):568-74.
- 3. Chang Y, et al. Structural basis for G9a-like protein lysine methyltransferase inhibition by BIX-01294. (2009) Nat Struct Mol Biol. 16(3):312-7.
- 4. Imai K, et al. Involvement of histone H3 lysine 9 (H3K9) methyltransferase G9a in the maintenance of HIV-1 latency and its reactivation by BIX01294. (2010) J Biol Chem. 285(22):16538-45.
- 5. Malmquist NA, et al. Small-molecule histone methyltransferase inhibitors display rapid antimalarial activity against all blood stage forms in Plasmodium falciparum. (2012) Proc Natl Acad Sci USA. 109(41):16708-13.
- 6. Kim Y, et al. BIX-01294 induces autophagy-associated cell death via EHMT2/G9a dysfunction and intracellular reactive oxygen species production. (2013) Autophagy. 9(12):2126-39.