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