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0003111079
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Duff, K.C.1
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6
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84920340785
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Ph.D Thesis (1995)
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Kolocouris, A. Ph.D Thesis (1995).
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Kolocouris, A.1
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7
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0028129705
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Kolocouris, N.; Foscolos, G. B.; Kolocouris A.; Marakos, P.; Pouli, N.; Fytas, G.; Ikeda, S.; De Clercq, E. J. Med. Chem. 1994, 37, 2896-2902.
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Kolocouris, N.1
Foscolos, G.B.2
Kolocouris, A.3
Marakos, P.4
Pouli, N.5
Fytas, G.6
Ikeda, S.7
De Clercq, E.8
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8
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10144256510
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Kolocouris, N.; Kolocouris A.; Foscolos G. B.; Fytas, G.; Neyts, J.; Padalko, E.; Balzarini, J.; Snoeck, R.; Andrei, G.; De Clercq, E. J. Med. Chem. 1996, 39, 3307-3318.
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J. Med. Chem.
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Kolocouris, N.1
Kolocouris, A.2
Foscolos, G.B.3
Fytas, G.4
Neyts, J.5
Padalko, E.6
Balzarini, J.7
Snoeck, R.8
Andrei, G.9
De Clercq, E.10
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10
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85038060574
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note
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3, 75 MHz) δ 25.3 (4-C), 27.0 (5-C), 28.0, 28.1, 28.3, 28.7 (7′,5′,3′,1′-C), 30.8 (3-C), 32.2, 32.5 (4′,9′-C), 38.4 (6′-C), 39.1, 39.5 (8′,10′-C), 47.7 (6-C), 49.9 (2′-C), 56.0 (2-C). Spectra and elemental analysis of all the synthesized compounds were in accord with their structure.
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11
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0023917192
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Shigeta, S.; Konno, K.; Yokota, T.; Nakamura, K.; De Clercq, E. Antimicrob. Agents Chemother. 1998, 32, 906-911.
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Shigeta, S.1
Konno, K.2
Yokota, T.3
Nakamura, K.4
De Clercq, E.5
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14
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0033587175
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- orientation around C2-C2′ bond. Conformers A-D with an anti orientation around C2-C2′ bond were found to have the lowest energy content. For further details see
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- orientation around C2-C2′ bond. Conformers A-D with an anti orientation around C2-C2′ bond were found to have the lowest energy content. For further details see: Mavromoustakos, T.; Kolocouris, A.; Zervou, M.; Roumelioti, P.; Matsoukas, J. M.; Weisemann, R. J. Med. Chem. 1999, 42, 1714-1722.
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J. Med. Chem.
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Mavromoustakos, T.1
Kolocouris, A.2
Zervou, M.3
Roumelioti, P.4
Matsoukas, J.M.5
Weisemann, R.6
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15
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33845379406
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Calculations of the relative energies of conformations A-D were performed using MM2 calculations. These calculations give the most consistent results with experimental data for six-membered nitrogen heterocycles as describen by. The MM+ force field provided by the Hyperchem was used. This force field is an extension of MM2 force field
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Calculations of the relative energies of conformations A-D were performed using MM2 calculations. These calculations give the most consistent results with experimental data for six-membered nitrogen heterocycles as describen by Profeta, S.; Allinger, N. L. J. Am. Chem. Soc. 1985, 107, 1907-1918. The MM+ force field provided by the Hyperchem was used. This force field is an extension of MM2 force field.
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J. Am. Chem. Soc.
, vol.107
, pp. 1907-1918
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Profeta, S.1
Allinger, N.L.2
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16
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0030743225
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Fytas, G.; Stamatiou, G.; Foscolos, G. B.; Kolocouris, A.; Kolocouris, N.; Witvrouw, M.; Pannecouque, C.; De Clercq, E. Bioorg. Med. Chem. Lett., 1997, 1887-1890.
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(1997)
Bioorg. Med. Chem. Lett.
, pp. 1887-1890
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Fytas, G.1
Stamatiou, G.2
Foscolos, G.B.3
Kolocouris, A.4
Kolocouris, N.5
Witvrouw, M.6
Pannecouque, C.7
De Clercq, E.8
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