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78149282854
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note
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R = 6.8, 8.9, 16.9, 17.2, 17.8 and 18.4 min (for compounds 6a, 6b, 9a, 9b, 13a and 13b, respectively).
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30
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78149284812
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note
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All the synthesized final analogues were generally preserved at 0 to -4 °C and remained stable for months. Even allowing them to stand at rt for several weeks did not lead to any decomposition (HPLC analysis). Besides, few of the final analogues (6a, 9a, 11a-b, 13a) were found to be soluble in chloroform but all of them were fairly soluble in methanol and dimethyl sulfoxide (DMSO) as well.
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31
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78149283212
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note
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8: C, 63.98; H, 7.61. Found: C, 64.02; H, 7.56.
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78149285145
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note
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50 values, that is, the concentration that inhibited 50% of cell growth, enumerated by graphic extrapolation using Graph pad prism software (version 5).
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36
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0023121146
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L.W. Hardy, J.S. Finer-Moore, W.R. Montfort, M.O. Jones, D.V. Santi, and R.M. Stroud Science 235 1987 448
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Hardy, L.W.1
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Stroud, R.M.6
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37
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78149282530
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note
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2, pH 7.4). Annexin V-FITC and propidium iodide were then added according to the manufacturer's instructions and incubated for 15 min in the dark at 25 °C. Data was acquired using a FACS Calibur flow cytometer and analyzed with Cell Quest Pro software.
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38
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78149279837
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note
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50 concentration (5.47 μM) of 6a (for 24 h), washed with ice cold PBS and stained with Hoechst 33258 (10 μg/ml, 30 min). The cells were mounted on poly l-lysine coated slides and analyzed in a laser scanning confocal microscope (Leica TCS SP2 system, Leica microsystem, Heidelberg, Germany; 100×). At least 20 microscopic fields were observed for each sample.
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