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6 cells/well). Cells were treated for 24 h with 10 μM compound. Following 24 h, cells were washed 2 times with 2.0 mL ice cold 0.9% sodium chloride saline. Cells were then scraped into 0.5 mL 70% methanol and frozen overnight to facilitate the extraction of nucleotide metabolites. Extracted cell material in 70% methanol was transferred into tubes and dried. After drying, samples were re-suspended in 1 mM ammonium phosphate pH 8.5. TP levels were quantitated using liquid chromatography coupled to triple quadrapole mass spectrometry by methods similar to those previously reported in
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6 cells/well). Cells were treated for 24 h with 10 μM compound. Following 24 h, cells were washed 2 times with 2.0 mL ice cold 0.9% sodium chloride saline. Cells were then scraped into 0.5 mL 70% methanol and frozen overnight to facilitate the extraction of nucleotide metabolites. Extracted cell material in 70% methanol was transferred into tubes and dried. After drying, samples were re-suspended in 1 mM ammonium phosphate pH 8.5. TP levels were quantitated using liquid chromatography coupled to triple quadrapole mass spectrometry by methods similar to those previously reported in L. Durand-Gasselin, K.K. Van Rompay, J.E. Vela, I.N. Henne, W.A. Lee, and G.R. Rhodes Mol. Pharm. 6 2009 1145
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