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84908533487
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note
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1H NMR (DMSO-d6, 600 MHz) δ(ppm): 6.885 (d, 1H), 7.071 (d, 1H), 7.235 (d, 1H), 7.354 (d, 1H), 7.506 (d, 1H), 7.541 (d, 1H), 7.747 (s, 1H), 7.835 (s,1H), 8.362 (s, 1H), 11.107 (s, 1H).
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16
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84908533486
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note
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1H NMR (DMSO-d6, 600 MHz) δ(ppm): 6.795 (d, 1H), 7.068 (d, 1H), 7.186 (d, 1H), 7.327 (d, 1H), 7.497 (d, 1H), 7. 527 (d, 1H), 7.794 (s, 1H) 8.062 (s, 1H).
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17
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84908533485
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note
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2) to convergence.
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19
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84904391523
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Synthesis, characterization, DNA binding and cleavage properties of a ternary copper(II) Schiff base complex
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X. Li, C.F. Bi, Y.H. Fan, X. Zhang, X.D. Wei, X.M. Meng, Synthesis, characterization, DNA binding and cleavage properties of a ternary copper(II) Schiff base complex, Transit. Met. Chem. 39 (2014) 577-584.
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Li, X.1
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Meng, X.M.6
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20
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84908533484
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note
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2. The cells were harvested, lysed and supernatants were collected as whole cell extracts used for western blot analysis.
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84908533483
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note
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MDA-MB-231 cells were seeded in triplicate in a 96-well plate and incubated at 37°C until 70-80% con fl uent, then treated with the indicated concentration of the complex and the ligand for 24 h. Media was then removed and MTT solution (1 mg/ml) was added followed by a 2 h incubation period. MTT was then removed and 100 μl DMSO added to dissolve the metabolized MTT product, followed by measuring the absorbance values on a Victor 3 multi-label plate reader (PerkinElmer Wellesley, MA).
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22
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84901648175
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Clioquinol and pyrrolidine dithiocarbamate complex with copper to form proteasome inhibitors and apoptosis inducers in human breast cancer cells
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K.G. Daniel, D. Chen, S. Orlu, Q.C. Cui, F.R. Miller, Q.P. Dou, Clioquinol and pyrrolidine dithiocarbamate complex with copper to form proteasome inhibitors and apoptosis inducers in human breast cancer cells, Breast Cancer Res. 7 (2005) 897-908.
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Daniel, K.G.1
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23
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78751493814
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24
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84908533482
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note
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MDA-MB-231 cells were treated as indicated, lysed and protein concentrations measured by the Bio-Rad Protein Assay (Bio-Rad Hercules, CA). Whole cell extracts (10 μg) were incubated for 2 h at 37°C in 100 μl of assay buffer (20 mM Tris-HCl, pH 7.5) with 20 μM fluorogenic peptide substrate Suc-LLVY-AMC. Proteasomal CT-like activity was measured using the Wallac Victor 3 Multi-label Counter with an excitation filter of 365 nm and emission filter of 460 nm.
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84908533481
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note
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Proteins (30 μg) from whole cell extracts were separated by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and transferred to a nitrocellulose membrane, followed by visualization with an enhanced chemiluminescence reagent (Denville Scientific Metuchen, NJ).
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28
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34249780515
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Structure-proteasome-inhibitory activity relationships of dietary flavonoids in human cancer cells
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D. Chen, M.S. Chen, Q.C. Cui, H. Yang, Q.P. Dou, Structure-proteasome-inhibitory activity relationships of dietary flavonoids in human cancer cells, Front. Biosci. 12 (2007) 1935-1945.
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0035918278
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Ester bond-containing tea polyphenols potently inhibit proteasome activity in vitro and in vivo
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Novel dipeptidyl proteasome inhibitors overcome Bcl-2 protective function and selectively accumulate the cyclin-dependent kinase inhibitor p27 and induce apoptosis in transformed, but not normal, human fibroblasts
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84908533480
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note
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Cellular morphology changes were observed using a Zeiss (Thornwood, NY) Axiovert 25 microscope with phase contrast.
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