S88858 |
3-amino-2-(3-amino-4-methoxyphenyl)chromen-4-one |
源葉(MedMol) | 98% |
- 產(chǎn)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
- 靶點: p70S6K;Proteasome
- 體外研究:
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
- 參考文獻:
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
- 保存條件: -20℃
- 配置溶液濃度參考:
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
- 注意:部分產(chǎn)品我司僅能提供部分信息,我司不保證所提供信息的權(quán)威性,僅供客戶參考交流研究之用。
輸入產(chǎn)品批號:
本計算器可幫助您計算出特定溶液中溶質(zhì)的質(zhì)量、溶液濃度和體積之間的關系,公式為:
質(zhì)量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)