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Henderson, B. W.; Busch, T. M.; Vaughan, L. A.; Frawley, N. P.; Babich, D.; Sosa, T. A.; Zollo, J. D.; Dee, A. S.; Cooper, M. T.; Bellnier, D. A.; Greco, W. R.; Oseroff, A. R. Cancer Res. 2000, 60, 525.
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Zollo, J.D.7
Dee, A.S.8
Cooper, M.T.9
Bellnier, D.A.10
Greco, W.R.11
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0642275173
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Rodriguez, M. E.; Moran, F.; Bonansea, A.; Monetti, M.; Fernandez, D. A.; Strassen, C. A.; Rivarola, V.; Awruch, J.; Dicelio, L. E. Photochem. Photobiol. Sci. 2003, 2, 988.
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Monetti, M.4
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Rivarola, V.7
Awruch, J.8
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Masuda, H.1
Odani, A.2
Yamazaki, T.3
Yajima, T.4
Yamauchi, O.5
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16
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85080497823
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Complex 2 was prepared from a reaction of CuCl2.2H 2O (0.17 g, 1.0 mmol) with an aqueous solution of L-arginine (0.23 g, 1.1 mmol) treated with NaOH (0.04 g, 1.0 mmol) and followed by slow addition of a methanolic solution of 1,10-phenanthroline (0.18 g, 0.9 mmol, The reaction mixture was stirred at 25 °C for 2 h and filtered. The filtrate on slow evaporation gave blue, rectangular-shaped single crystals suitable for X-ray diffraction. The crystals were isolated and washed with aqueous methanol (1:1 v/v) before drying over P4O10 [Yield: ∼75, The complex showed good solubility in water, methanol, ethanol, N,N-dimethylformamide (DMF, and dimethyl sulfoxide (DMSO, The ternary structure is stable in solution. Anal. Calcd for C18H22Cl 2CuN6O2 (2, C, 44.22; H, 4.54; N, 17.19. Found: C, 44.12; H, 4.45; N, 16.94. IR KBr phase, 3373br, 3194br, 3027br, 1684s
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B.
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17
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85080591228
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Crystal data for 2·2.5H2O: C18H 27Cl2CuN6O4.5, M, 533.90, triclinic, space group P1 (No. 1, a, 10.359(6) Å, b, 12.437(7) Å, c, 18.888(11) Å, α, 94.599(9)°, β, 104.701(9)°, γ, 101.002(9)°, V, 2289(2) Å3, Z, 4, ρ, 1.549 g cm-3, T, 293(2) K, 1.89° ≤ θ ≤ 26.00°, μ= 12.27 cm-1, F(000, 1104, R1, 0.0454, wR2, 0.1226 for 14 046 reflections with I > 2σ(I) and 1136 parameters [R1-(F2, 0.0588 (all data, Weighting scheme: w, 1/[σ2 (Fo2, 0.0823P)2, 0.0P, where P, Fo2, 2Fc2]/3. The GOF and the largest difference peak were 1.025 and 0.934 e
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-3, respectively. Perspective view of the complex was obtained by ORTEP. Data were collected using Bruker SMART APEX CCD diffractometer with a Mo Kα X-ray source. The structure was solved and refined using the SHELX program (Sheldrick, G. M. SHELX-97, Programs for Crystal Structure Solution and Refinement; University of Göttingen: Göttingen, Germany, 1997).
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18
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0024804717
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m values for ntp, 1 and 2 are 18, 3, 2 with CT-DNA and 38, 11, 8 °C with poly(dA)·poly(dT), respectively.
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m values for ntp, 1 and 2 are 18, 3, 2 with CT-DNA and 38, 11, 8 °C with poly(dA)·poly(dT), respectively.
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19
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33244455448
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2 (NBD code GDLB05) was obtained from the protein data bank. Some important H-bonding parameters (Å) for 1 in the docked state are H(N8)-O(A19), 2.65; H(N13)-O(T6), 2.78 (Figure S5a); in 2: H(N12)-O(T6), 2.96; H(N5)-O3(A20), 2.68; H(N9)-N3(A20), 3.04 (Figure S5b). Mondal, S.; Vijayan, R.; Shichina, K.; Babu, R. M.; Ramakumar, S. In Silico Biol. 2005, 5, 557.
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2 (NBD code GDLB05) was obtained from the protein data bank. Some important H-bonding parameters (Å) for 1 in the docked state are H(N8)-O(A19), 2.65; H(N13)-O(T6), 2.78 (Figure S5a); in 2: H(N12)-O(T6), 2.96; H(N5)-O3(A20), 2.68; H(N9)-N3(A20), 3.04 (Figure S5b). Mondal, S.; Vijayan, R.; Shichina, K.; Babu, R. M.; Ramakumar, S. In Silico Biol. 2005, 5, 557.
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20
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85080611217
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2 1.8 mm ± 10%, beam divergence 0.7 mrad ± 10%). The complex and reagent concentrations correspond to those in the 20 μL sample solution path-length = 5 mm). The extent of DNA cleavage was measured from the intensities of the bands in agarose gels using UVITECH Gel Documentation System giving an intensity measurement error of ∼5%.
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2 1.8 mm ± 10%, beam divergence 0.7 mrad ± 10%). The complex and reagent concentrations correspond to those in the 20 μL sample volume (solution path-length = 5 mm). The extent of DNA cleavage was measured from the intensities of the bands in agarose gels using UVITECH Gel Documentation System giving an intensity measurement error of ∼5%.
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22
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0141992314
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Dhar, S.; Senapati, D.; Das, P. K.; Chattopadhyay, P.; Nethaji, M.; Chakravarty, A. R. J. Am. Chem. Soc. 2003, 125, 12118.
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(2003)
J. Am. Chem. Soc
, vol.125
, pp. 12118
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Dhar, S.1
Senapati, D.2
Das, P.K.3
Chattopadhyay, P.4
Nethaji, M.5
Chakravarty, A.R.6
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23
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21844449406
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Szacilowski, K.; Macyk, W.; Drzewiecka-Matuszek, A.; Brindell, M.; Stochel, G. Chem. Rev. 2005, 105, 2647.
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(2005)
Chem. Rev
, vol.105
, pp. 2647
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Szacilowski, K.1
Macyk, W.2
Drzewiecka-Matuszek, A.3
Brindell, M.4
Stochel, G.5
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