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62149096843
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note
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6: C, 64.96; H, 6.61; N, 6.89. Found: C, 65.00; H, 6.78; N, 6.93.
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62149087443
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note
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50 values were calculated from individual inhibition curves plotted by Grafit software. The same method was used to determine cytotoxicity against HT29-AK and MDA-MB-231 cells at drug concentrations up to 750 μM.
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0017311840
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For in vitro antimalarial assessment versus the 3D7 strain of Plasmodium falciparum the following protocol was employed. Parasites were maintained in continuous culture using the method of Jensen and Trager:
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0018606732
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Antimalarial activity was assessed with an adaption of the 48 hr sensitivity assay of Desjardins et al. using [3H]-hypoxanthine incorporation as an assessment of parasite growth:
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Antimalarial activity was assessed with an adaption of the 48 hr sensitivity assay of Desjardins et al. using [3H]-hypoxanthine incorporation as an assessment of parasite growth:. Desjardins R.E., Canfield C.J., Haynes J.D., Chulay J.D. Antimicrob. Agents Chemother. 16 (1979) 710-718
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24
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62149093250
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note
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5 cells) were washed in HBSS and the resultant cell pellet was resuspended in 500 μL of TMRE solution (50 nM in HBSS) and incubated for 10 min at 37 °C. A minimum of 500 cells were measured by flow cytometry on fluorescence channel FL-2 (Coulter Epics, XL Software). The data was analysed using WinMDI, v2.8 software (Scripps Institute, California, USA).
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25
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62149116525
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note
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6) were washed twice in HBSS, fixed in 1 mL of ice-cold 70% ethanol, and frozen at -20 °C. After 2 h the 70% ethanol was removed and the cell pellet was resuspended in 1 mL of PI stock solution (phosphate-buffered saline containing 40 μg/mL PI, 0.1 mg/mL RNase, and 3.8 mM sodium citrate)) and incubated at 37 °C (30 min). A minimum of 5000 cells were analysed by flow cytometry. PI fluorescence was measured on fluorescence channel FL-2. The proportion of cells in each stage of the cell cycle was calculated from the DNA content of the cell using WinMDI, v2.8 software.
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