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77956896734
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note
-
3OH, 20:1). The purified material was dried in vacuo to afford the corresponding products.
-
-
-
-
40
-
-
77956921696
-
-
note
-
2 for 48 h. The number of viable cells remaining after the appropriate treatment was determined by (3-(4,5-dimethylthiazol-2-yl)-2,5- diphenyltetrazolium bromide, MTT) colorimetric assay.
-
-
-
-
41
-
-
77956933449
-
-
note
-
-1 (-CC-).
-
-
-
-
42
-
-
77956931812
-
-
note
-
+ 407.0349, found 407.0345.
-
-
-
-
43
-
-
77956940028
-
-
note
-
6 cells, evaluating the sub-G1/G0 ratio. Each sample was performed in triplicate.
-
-
-
-
44
-
-
77956904153
-
-
note
-
Caspase-3/7 cleavage assay: MiaPaCa-2 cells were initially seeded at 15,000 cells/well on 96-well plates. Twenty-four hours later, cells were treated with the test compound for 48 h. Next 100 μL of Caspase-Glo 3/7 Assay Reagent (Promega) was added to each well of a white 96-well plate containing 100 μL of blank, negative control cells or treated cells in culture medium. The caspase-3/7 activity was measured by the cleavage of the luminogenic substrate containing the tetrapeptide sequence DEVD according to the instructions of the manufacturer (Promega). The plate was incubated at room temperature for 1 h before measuring the luminescence of each well. Each experiment was performed in triplicate.
-
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45
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0026324313
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46
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77956917105
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-
note
-
2. Then the cells were harvested and DNA synthesis activity was determined according to the radioactivity by using liquid scintillation counting.
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