AAAAAA

   
Results: 1-9 |
Results: 9
Human immunodeficiency virus type 1 central DNA flap: Dynamic terminal product of plus-strand displacement DNA synthesis catalyzed by reverse transcriptase assisted by nucleocapsid protein
Authors: Hameau, L Jeusset, J Lafosse, S Coulaud, D Delain, E Unge, T Restle, T Le Cam, E Mirambeau, G
Citation: L. Hameau et al., Human immunodeficiency virus type 1 central DNA flap: Dynamic terminal product of plus-strand displacement DNA synthesis catalyzed by reverse transcriptase assisted by nucleocapsid protein, J VIROLOGY, 75(7), 2001, pp. 3301-3313
Synthesis of novel, potent, diol-based HIV-1 protease inhibitors via intermolecular pinacol homocoupling of (2S)-2-benzyloxymethyl-4-phenylbutanal
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
Synthesis and comparative molecular field analysis (CoMFA) of symmetric and nonsymmetric cyclic sulfamide HIV-1 protease inhibitors
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
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
Monoclonal antibodies to native HIV type 1 reverse transcriptase and theirinteraction with enzymes from different subtypes
Authors: Rytting, AS Akerblom, L Albert, J Unge, T Bjorling, E Al-Khalili, L Gronowitz, JS Kallander, CFR
Citation: As. Rytting et al., Monoclonal antibodies to native HIV type 1 reverse transcriptase and theirinteraction with enzymes from different subtypes, AIDS RES H, 16(13), 2000, pp. 1281-1294
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
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
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
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: 1-9 |