S88858 |
3-amino-2-(3-amino-4-methoxyphenyl)chromen-4-one |
源叶(MedMol) | 98% |
- 产品描述: DD1, a proteasome inhibitor, targets Bax activation and P70S6K degradation during acute myeloid leukemia (AML) apoptosis. DD1 induces apoptosis in the caspase-dependent manner. DD1 induces mitochondrial membrane depolarization and Bad dephosphorylation
- 靶点: p70S6K;Proteasome
- 体外研究:
DD1 (20 μM; 96 h) shows antiproliferation activity in a dose- and time-dependent manner in U937 cells. DD1 induces cell cycle arrest at G2/M phase and apoptosis. DD1 (10, 20 μM; 48 h) induces mitochondrial membrane depolarization, Bax upregulation and Bad dephosphorylation. DD1 (2-20 μM; 40 h) shows inhibitor for chymotrypsin-like activity in U937 lysates
- 参考文献:
1. Marion Piedfer, et al. p70S6 kinase is a target of the novel proteasome inhibitor 3,3'-diamino-4'-methoxyflavone during apoptosis in human myeloid tumor cells. Biochim Biophys Acta. 2013 Jun;1833(6):1316-28.
- 溶解性: DMSO
- 保存条件: -20℃
- 配置溶液浓度参考:
1mg 5mg 10mg 1 mM 3.542 ml 17.712 ml 35.424 ml 5 mM 0.708 ml 3.542 ml 7.085 ml 10 mM 0.354 ml 1.771 ml 3.542 ml 50 mM 0.071 ml 0.354 ml 0.708 ml
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质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)