AAAAAA

   
Results: 1-12 |
Results: 12

Authors: Brun, V Legraverend, M Grierson, DS
Citation: V. Brun et al., Cyclin-dependent kinase (CDK) inhibitors: development of a general strategy for the construction of 2,6,9-trisubstituted purine libraries. Part I, TETRAHEDR L, 42(46), 2001, pp. 8161-8164

Authors: Brun, V Legraverend, M Grierson, DS
Citation: V. Brun et al., Cyclin-dependent kinase (CDK) inhibitors: development of a general strategy for the construction of 2,6,9-trisubstituted purine libraries. Part 2, TETRAHEDR L, 42(46), 2001, pp. 8165-8167

Authors: Brun, V Legraverend, M Grierson, DS
Citation: V. Brun et al., Cyclin-dependent kinase (CDK) inhibitors: development of a general strategy for the construction of 2,6,9-trisubstituted purine libraries. Part 3, TETRAHEDR L, 42(46), 2001, pp. 8169-8171

Authors: Janin, YL Huel, C Legraverend, M Aubertin, AM Bisagni, E
Citation: Yl. Janin et al., Syntheses of 4-benzylpyridones via nucleophilic aromatic substitutions, SYNTHESIS-S, (12), 2001, pp. 1806-1811

Authors: Legraverend, M Ludwig, O Leclerc, S Meijer, L
Citation: M. Legraverend et al., Synthesis of a new series of purine derivatives and their anti-cyclin-dependent kinase activities, J HETERO CH, 38(1), 2001, pp. 299-303

Authors: Legraverend, M Tunnah, P Noble, M Ducrot, P Ludwig, O Grierson, DS Leost, M Meijer, L Endicott, J
Citation: M. Legraverend et al., Cyclin-dependent kinase inhibition by new C-2 alkynylated purine derivatives and molecular structure of a CDK2-inhibitor complex, J MED CHEM, 43(7), 2000, pp. 1282-1292

Authors: Ducrot, P Legraverend, M Grierson, DS
Citation: P. Ducrot et al., 3D-QSAR CoMFA on cyclin-dependent kinase inhibitors, J MED CHEM, 43(22), 2000, pp. 4098-4108

Authors: Dolle, V Nguyen, CH Legraverend, M Aubertin, AM Kirn, A Andreola, ML Ventura, M Tarrago-Litvak, L Bisagni, E
Citation: V. Dolle et al., Synthesis and antiviral activity of 4-benzyl pyridinone derivatives as potent and selective non-nucleoside human immunodeficiency virus type 1 reverse transcriptase inhibitors, J MED CHEM, 43(21), 2000, pp. 3949-3962

Authors: Pontikis, R Dolle, V Guillaumel, J Dechaux, E Note, R Nguyen, CH Legraverend, M Bisagni, E Aubertin, AM Grierson, DS Monneret, C
Citation: R. Pontikis et al., Synthesis and evaluation of "AZT-HEPT", "AZT-pyridinone", and "ddC-HEPT" conjugates as inhibitors of HIV reverse transcriptase, J MED CHEM, 43(10), 2000, pp. 1927-1939

Authors: Legraverend, M Ludwig, O Bisagni, E Leclerc, S Meijer, L Giocanti, N Sadri, R Favaudon, V
Citation: M. Legraverend et al., Synthesis and in vitro evaluation of novel 2,6,9-trisubstituted purines acting as cyclin-dependent kinase inhibitors, BIO MED CH, 7(7), 1999, pp. 1281-1293

Authors: Ventura, M Tarrago-Litvak, L Dolle, V Nguyen, CH Legraverend, M Fleury, HJA Litvak, S
Citation: M. Ventura et al., Effect of nucleoside analogs and non-nucleoside inhibitors of HIV-1 reverse transcriptase on cell-free virions, ARCH VIROL, 144(3), 1999, pp. 513-523

Authors: Janin, YL Chiki, J Legraverend, M Huel, C Bisagni, E
Citation: Yl. Janin et al., On the methylation of 3-cyano-6-hydroxypyridine-2(1H)-ones, TETRAHEDRON, 55(44), 1999, pp. 12797-12804
Risultati: 1-12 |