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Results: 1-6 |
Results: 6

Authors: Pyring, D Lindberg, J Rosenquist, A Zuccarello, G Kvarnstrom, I Zhang, H Vrang, L Unge, T Classon, B Hallberg, A Samuelsson, B
Citation: D. Pyring et al., Design and synthesis of potent C-2-symmetric diol-based HIV-1 protease inhibitors: Effects of fluoro substitution, J MED CHEM, 44(19), 2001, pp. 3083-3091

Authors: Wachtmeister, J Muhlman, A Classon, B Kvarnstrom, I Hallberg, A Samuelsson, B
Citation: J. Wachtmeister et al., Impact of the central hydroxyl groups on the activity of symmetrical HIV-1protease inhibitors derived from L-mannaric acid, TETRAHEDRON, 56(20), 2000, pp. 3219-3225

Authors: Noteberg, D Branalt, J Kvarnstrom, I Linschoten, M Musil, D Nystrom, JE Zuccarello, G Samuelsson, B
Citation: D. Noteberg et al., New proline mimetics: Synthesis of thrombin inhibitors incorporating cyclopentane- and cyclopentenedicarboxylic acid templates in the P2 position. Binding conformation investigated by X-ray crystallography, J MED CHEM, 43(9), 2000, pp. 1705-1713

Authors: Oscarsson, K Classon, B Kvarnstrom, I Hallberg, A Samuelsson, B
Citation: K. Oscarsson et al., Solid phase assisted synthesis of HIV-1 protease inhibitors. Expedient entry to unsymmetrical substitution of a C-2 symmetric template, CAN J CHEM, 78(6), 2000, pp. 829-837

Authors: Hulten, J Andersson, HO Schaal, W Danielson, HU Classon, B Kvarnstrom, I Karlen, A Unge, T Samuelsson, B Hallberg, A
Citation: J. Hulten et al., Inhibitors of the C-2-symmetric HIV-1 protease: Nonsymmetric binding of a symmetric cyclic sulfamide with ketoxime groups in the P2/P2 ' side chains, J MED CHEM, 42(20), 1999, pp. 4054-4061

Authors: Alterman, M Andersson, HO Garg, N Ahlsen, G Lovgren, S Classon, B Danielson, UH Kvarnstrom, I Vrang, L Unge, T Samuelsson, B Hallberg, A
Citation: M. Alterman et al., Design and fast synthesis of C-terminal duplicated potent C-2-symmetric P1/P1 '-modified HIV-1 protease inhibitors, J MED CHEM, 42(19), 1999, pp. 3835-3844
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