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0029795726
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17
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0013523878
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note
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2O of these five new derivatives are summarized as follows: 7, δ: 8.11 (1H, s), 7.84 (1H, s), 5.36 (1H, d; J = 15.4 Hz), 5.17 (1H, d; J = 15.4 Hz), 4.80 (1H, d; J = 4.8 Hz), 4.74 (1H, m), 4.57 (1H, s), 4.03 (1H, dd; J = 4.8 Hz), 1.42 (3H, s), 1.34 (3H, s); 10, δ: 8.12 (1H, s), 7.85 (1H, s), 5.37 (1H, d; J = 15.4 Hz), 5.16 (1H, d; J = 15.4 Hz), 5.08 (1H, d; J = 4.6 Hz), 4.57 (1H, s), 4.38-4.31 (1H, m), 4.28-3.98 (2H, m), 1.41 (3H, s); 25, δ: 6.68 (1H, d; J = 12.4 Hz), 6.16 (1H, d; J = 12.4 Hz), 5.25 (1H, d; J = 4.7 Hz), 4.36 (1H, m), 4.22 1H, dd; 7=8.16 Hz), 4.08 (1H, dd; 7 = 8.16 Hz), 1.94 (3H, s); 26, δ: 7.08 (1H, d; J = 16.5 Hz), 6.07 (1H, d; J = 16.5 Hz), 5.2 (1H, s), 4.36 (1H, m), 4.21 (1H, dd; J = 8.10 Hz), 4.07 (1H, dd; J = 8.10 Hz), 1.64 (3H, s); 29, δ: 7.68 (1H, s), 5.18 (1H, d; J = 4.5 Hz), 4.88 (1H, s), 4.35 (1H, m), 4.2 (1H, t), 4.08 (1H, dd), 3.97 (3H, s), 1.66 (3H, s).
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18
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0013514239
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12. Maiti, S. N.; Spevak, P.; Wong, R.; Reddy, N. A. V.; Micetich, R. G.; Ogawa, K. Heterocycles 1991, 32, 1505.
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19
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0000264975
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21
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0031023673
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15. Czajkowski, D. P.; Reddy, A. V. N.; Setti, E. L.; Phillips, O. A.; Micetich, R. G.; Kunugita, C.; Maiti, S. N. Bioorg. Med. Chem. Lett. 1997, 7, 11.
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Czajkowski, D.P.1
Reddy, A.V.N.2
Setti, E.L.3
Phillips, O.A.4
Micetich, R.G.5
Kunugita, C.6
Maiti, S.N.7
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23
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0013525345
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note
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17. Molecular modelling studies using MacroModel v6.0 showed that good binding ligands fit well in the enzyme active site and remained there during the molecular dynamics simulation. Details of the molecular modelling studies will be published elsewhere.
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