|Solubility:||DMSO up to 50 mM|
|Chemical Name:||(4-amino-6-(phenylamino)-1,3,5-triazin-2-yl)methyl 4-nitrobenzoate|
|Storage:||Powder: 4oC 1 year. DMSO: 4oC 3 month; -20oC 1 year.|
TZ9 is a selective and cell permeable inhibitor of human E2 ubiquitin-conjugating enzyme Rad6B. It binds to the Rad6B catalytic site, inhibits Rad6B-induced histone H2A ubiquitination, downregulates intracellular β-catenin. It can induce G2/M arrest and apoptosis, and inhibit proliferation and migration of metastatic human breast cancer cells (IC50 ~6 µM).
How to Use:
In vitro: TZ9 was used at 10-50 µM final concentration in vitro and in cellular assays.
In vivo: n/a
- 1. Sanders MA, et al. Novel inhibitors of Rad6 ubiquitin conjugating enzyme: design, synthesis, identification, and functional characterization. (2013) Mol Cancer Ther. 12(4):373-83.
Products are for research use only. Not for human use.
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