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Results: 1-7 |
Results: 7
Anti-HIV type 1 activity of 3 '-fluoro-3 '-deoxythymidine for several different multidrug-resistant mutants
Authors: Kim, EY Vrang, L Oberg, B Merigan, TC
Citation: Ey. Kim et al., Anti-HIV type 1 activity of 3 '-fluoro-3 '-deoxythymidine for several different multidrug-resistant mutants, AIDS RES H, 17(5), 2001, pp. 401-407
Design and synthesis of potent C-2-symmetric diol-based HIV-1 protease inhibitors: Effects of fluoro substitution
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
Characterization of a set of HIV-1 protease inhibitors using binding kinetics data from a biosensor-based screen
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
Bioisosteric modification of PETT-HIV-1 RT-inhibitors: Synthesis and biological evaluation
Authors: Hogberg, M Engelhardt, P Vrang, L Zhang, H
Citation: M. Hogberg et al., Bioisosteric modification of PETT-HIV-1 RT-inhibitors: Synthesis and biological evaluation, BIOORG MED, 10(3), 2000, pp. 265-268
Urea-PETT compounds as a new class of HIV-1 reverse transcriptase inhibitors. 3. Synthesis and further structure-activity relationship studies of PETT analogues. (vol 42, pg 4145, 1999)
Authors: Hogberg, M Sahlberg, C Engelhardt, P Noreen, R Kangasmetsa, J Johansson, NG Oberg, B Vrang, L Zhang, H Sahlberg, BL Unge, T Lovgren, S Fridborg, K Backbro, K
Citation: M. Hogberg et al., Urea-PETT compounds as a new class of HIV-1 reverse transcriptase inhibitors. 3. Synthesis and further structure-activity relationship studies of PETT analogues. (vol 42, pg 4145, 1999), J MED CHEM, 43(2), 2000, pp. 304-304
Urea-PETT compounds as a new class of HIV-1 reverse transcriptase inhibitors. 3. Synthesis and further structure-activity relationship studies of PETT analogues
Authors: Hogberg, M Sahlberg, C Engelhardt, P Noreen, R Kangasmetsa, J Johansson, NG Oberg, B Vrang, L Zhang, H Sahlberg, BL Unge, T Lovgren, S Fridborg, K Backbro, K
Citation: M. Hogberg et al., Urea-PETT compounds as a new class of HIV-1 reverse transcriptase inhibitors. 3. Synthesis and further structure-activity relationship studies of PETT analogues, J MED CHEM, 42(20), 1999, pp. 4150-4160
Design and fast synthesis of C-terminal duplicated potent C-2-symmetric P1/P1 '-modified HIV-1 protease inhibitors
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: 1-7 |