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Results: 1-11 |
Results: 11

Authors: Alterman, M Sjobom, H Safsten, P Markgren, PO Danielson, UH Hamalainen, M Lofas, S Hulten, J Classon, B Samuelsson, B Hallberg, A
Citation: M. Alterman et al., P1/P1 ' modified HIV protease inhibitors as tools in two new sensitive surface plasmon resonance biosensor screening assays, EUR J PH SC, 13(2), 2001, pp. 203-212

Authors: Muhlman, A Classon, B Hallberg, A Samuelsson, B
Citation: A. Muhlman et al., Synthesis of potent C-2-symmetric, diol-based HIV-1 protease inhibitors. Investigation of thioalkyl and thioaryl P1/P1 ' substituents, J MED CHEM, 44(21), 2001, pp. 3402-3406

Authors: Muhlman, A Lindberg, J Classon, B Unge, T Hallberg, A Samuelsson, B
Citation: A. Muhlman et al., Synthesis of novel, potent, diol-based HIV-1 protease inhibitors via intermolecular pinacol homocoupling of (2S)-2-benzyloxymethyl-4-phenylbutanal, J MED CHEM, 44(21), 2001, pp. 3407-3416

Authors: Schaal, W Karlsson, A Ahlsen, G Lindberg, J Andersson, HO Danielson, UH Classon, B Unge, T Samuelsson, B Hulten, J Hallberg, A Karlen, A
Citation: W. Schaal et al., Synthesis and comparative molecular field analysis (CoMFA) of symmetric and nonsymmetric cyclic sulfamide HIV-1 protease inhibitors, J MED CHEM, 44(2), 2001, pp. 155-169

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: Hamalainen, MD Markgren, PO Schaal, W Karlen, A Classon, B Vrang, L Samuelsson, B Hallberg, A Danielson, UH
Citation: Md. Hamalainen et al., Characterization of a set of HIV-1 protease inhibitors using binding kinetics data from a biosensor-based screen, J BIOMOL SC, 5(5), 2000, pp. 353-359

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: 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: Wachtmeister, J Muhlman, A Classon, B Samuelsson, B
Citation: J. Wachtmeister et al., Synthesis of 4-substituted carbocyclic 2,3-dideoxy-3-C-hydroxymethyl nucleoside analogues as potential anti-viral agents, TETRAHEDRON, 55(35), 1999, pp. 10761-10770

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
Risultati: 1-11 |