Name | 3-amino-2-(3-amino-4-methoxyphenyl)chromen-4-one |
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Synonyms |
3,3'-Diamino-4'-methoxyflavone
DD1 |
Description | 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[1]. |
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Related Catalog | |
In Vitro | DD1 (20 μM; 96 h) shows antiproliferation activity in a dose- and time-dependent manner in U937 cells[1]. DD1 induces cell cycle arrest at G2/M phase and apoptosis[1]. DD1 (10, 20 μM; 48 h) induces mitochondrial membrane depolarization, Bax upregulation and Bad dephosphorylation[1]. DD1 (2-20 μM; 40 h) shows inhibitor for chymotrypsin-like activity in U937 lysates[1]. |
References |
Density | 1.337g/cm3 |
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Boiling Point | 479.2ºC at 760 mmHg |
Molecular Formula | C16H14N2O3 |
Molecular Weight | 282.29400 |
Flash Point | 233.6ºC |
Exact Mass | 282.10000 |
PSA | 91.48000 |
LogP | 3.79540 |
Vapour Pressure | 2.4E-09mmHg at 25°C |
Index of Refraction | 1.667 |
Storage condition | -20°C |