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Results: 1-14 |
Results: 14

Authors: Courcambeck, J Bihel, F De Michelis, C Quelever, G Kraus, JL
Citation: J. Courcambeck et al., Design of potential new HIV protease inhibitors: enantioconvergent synthesis of new pyrrolidin-3-ol, and pyrrolidin-3-one peptide conjugates, J CHEM S P1, (12), 2001, pp. 1421-1430

Authors: Petit, A Bihel, F da Costa, CA Pourquie, O Checler, F Kraus, JL
Citation: A. Petit et al., New protease inhibitors prevent gamma-secretase-mediated production of A beta 40/42 without affecting Notch cleavage, NAT CELL BI, 3(5), 2001, pp. 507-511

Authors: Vlieghe, P Bihel, F Clerc, T Pannecouque, C Witvrouw, M De Clercq, E Salles, JP Chermann, JC Kraus, JL
Citation: P. Vlieghe et al., New 3 '-azido-3 '-deoxythymidin-5 '-yl O-(omega-hydroxyalkyl) carbonate prodrugs: Synthesis and anti-HIV evaluation, J MED CHEM, 44(5), 2001, pp. 777-786

Authors: Vlieghe, P Clerc, T Pannecouque, C Witvrouw, M De Clercq, E Salles, JP Kraus, JL
Citation: P. Vlieghe et al., New 3 '-azido-3 '-deoxythymidin-5 '-yl O-(4-hydroxyalkyl or -alkenyl or -alkylepoxide) carbonate prodrugs: Synthesis and anti-HIV evaluation, J MED CHEM, 44(18), 2001, pp. 3014-3021

Authors: Mourier, N Camplo, M Della Bruna, GS Pellacini, F Ungheri, D Chermann, JC Kraus, JL
Citation: N. Mourier et al., Synthesis and anti-HIV evaluation of new 2 ',3 '-dideoxy-3 '-thiacytidine prodrugs, NUCLEOS NUC, 19(7), 2000, pp. 1057-1091

Authors: Hantz, O Kraus, JL Zoulim, F
Citation: O. Hantz et al., Design and evaluation of hepatitis B virus inhibitors, CUR PHARM D, 6(5), 2000, pp. 503-523

Authors: De Michelis, C Rocheblave, L Priem, G Chermann, JC Kraus, JL
Citation: C. De Michelis et al., New anti-HIV derivatives: Synthesis and antiviral evaluation, BIO MED CH, 8(6), 2000, pp. 1253-1262

Authors: Kraus, JL Bouygues, M Courcambeck, J Chermann, JC
Citation: Jl. Kraus et al., Use of proline bioisosteres in potential HIV protease inhibitors: Phenylalanine-2-thiophenoxy-3-pyrrolidinone: Synthesis and anti-HIV evaluation, BIOORG MED, 10(17), 2000, pp. 2023-2026

Authors: Priem, G Rocheblave, L De Michelis, C Courcambeck, J Kraus, JL
Citation: G. Priem et al., Synthesis and chemical reactivity of thiophenoxyphenylalanine bioisosteres, suitable synthons for the design of HIV protease inhibitors, J CHEM S P1, (5), 2000, pp. 819-824

Authors: Camplo, M Mourier, N Chermann, JC Kraus, JL
Citation: M. Camplo et al., Synthesis and biological evaluation of polyaminated 2 ',3 '-dideoxy-3 '-thiacytidine prodrugs, NUCLEOS NUC, 18(4-5), 1999, pp. 879-880

Authors: Dessolin, J Galea, P Vlieghe, P Chermann, JC Kraus, JL
Citation: J. Dessolin et al., New polyazamacrocycle-nucleoside conjugates : Synthesis, anti-HIV evaluation and interaction with CXCR-4 coreceptor, NUCLEOS NUC, 18(4-5), 1999, pp. 881-882

Authors: Medou, M Priem, G Rocheblave, L Pepe, G Meyer, M Chermann, JC Kraus, JL
Citation: M. Medou et al., Synthesis and anti-HIV activity of alpha-thiophenoxy-hydroxyethylamide derivatives, EUR J MED C, 34(7-8), 1999, pp. 625-638

Authors: Rocheblave, L Priem, G De Michelis, C Kraus, JL
Citation: L. Rocheblave et al., Potent HIV protease inhibitors containing a novel (2-phenylsulfanyl-1-hydroxyethyl)amide isostere, TETRAHEDR L, 40(22), 1999, pp. 4173-4176

Authors: Dessolin, J Galea, P Vlieghe, P Chermann, JC Kraus, JL
Citation: J. Dessolin et al., New Bicyclam-AZT conjugates: Design, synthesis, Anti-HIV evaluation, and their interaction with CXCR-4 coreceptor, J MED CHEM, 42(2), 1999, pp. 229-241
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