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Results: 1-13 |
Results: 13

Authors: Golisade, A Herforth, C Wieking, K Kunick, C Link, A
Citation: A. Golisade et al., Biotin labelling of amines by polymer-assisted solution-phase synthesis, BIOORG MED, 11(13), 2001, pp. 1783-1786

Authors: Schultz, C Link, A Kunick, C
Citation: C. Schultz et al., Aryl rings are part of the darpone pharmacophore, ARCH PHARM, 334(5), 2001, pp. 163-166

Authors: Kunick, C Schultz, C Lemcke, T Zaharevitz, DW Gussio, R Jalluri, RK Sausville, EA Leost, M Meijer, L
Citation: C. Kunick et al., 2-substituted paullones: CDK1/cyclin B-inhibiting property and in vitro antiproliferative activity, BIOORG MED, 10(6), 2000, pp. 567-569

Authors: Gussio, R Zaharevitz, DW McGrath, CF Pattabiraman, N Kellogg, GE Schultz, C Link, A Kunick, C Leost, M Meijer, L Sausville, EA
Citation: R. Gussio et al., Structure-based design modifications of the paullone molecular scaffold for cyclin-dependent kinase inhibition, ANTI-CAN DR, 15(1), 2000, pp. 53-66

Authors: Leost, M Schultz, C Link, A Wu, YZ Biernat, J Mandelkow, EM Bibb, JA Snyder, GL Greengard, P Zaharevitz, DW Gussio, R Senderowicz, AM Sausville, EA Kunick, C Meijer, L
Citation: M. Leost et al., Paullones are potent inhibitors of glycogen synthase kinase-3 beta and cyclin-dependent kinase 5/p25, EUR J BIOCH, 267(19), 2000, pp. 5983-5994

Authors: Kunick, C
Citation: C. Kunick, Fused azepinones with antitumor activity, CUR PHARM D, 5(3), 1999, pp. 181-194

Authors: Sausville, EA Zaharevitz, D Gussio, R Meijer, L Louarn-Leost, M Kunick, C Schultz, R Lahusen, T Headlee, D Stinson, S Arbuck, SG Senderowicz, A
Citation: Ea. Sausville et al., Cyclin-dependent kinases: Initial approaches to exploit a novel therapeutic target, PHARM THERA, 82(2-3), 1999, pp. 285-292

Authors: Bleeker, C Kunick, C
Citation: C. Bleeker et C. Kunick, Naphthannelated azepinones: synthesis and antitumor activity, PHARMAZIE, 54(9), 1999, pp. 645-650

Authors: Link, A Zaharevitz, DW Kunick, C
Citation: A. Link et al., Antitumor pyrido[3,2-d][1]benzazepines: Synthesis and in vitro activity ofthiophene analogs, PHARMAZIE, 54(3), 1999, pp. 163-166

Authors: Van Calenbergh, S Link, A Kunick, C Herdewijn, P
Citation: S. Van Calenbergh et al., Exploration of the effect of sterically demanding 3 '-amino substitution of 3 '-deoxyadenosines towards inhibition of cyclin-dependent kinase 1 (vol 54, pg 727, 1999), PHARMAZIE, 54(12), 1999, pp. 892-892

Authors: Van Calenbergh, S Link, A Kunick, C Herdewijn, P
Citation: S. Van Calenbergh et al., Exploration of the effect of sterically demanding 3 '-amido substitution of 3 '-deoxyadenosines towards inhibition of cyclin-dependent kinase 1, PHARMAZIE, 54(10), 1999, pp. 727-729

Authors: Schultz, C Link, A Leost, M Zaharevitz, DW Gussio, R Sausville, EA Meijer, L Kunick, C
Citation: C. Schultz et al., Paullones, a series of cyclin-dependent kinase inhibitors: Synthesis, evaluation of CDK1/cyclin B inhibition, and in vitro antitumor activity, J MED CHEM, 42(15), 1999, pp. 2909-2919

Authors: Zaharevitz, DW Gussio, R Leost, M Senderowicz, AM Lahusen, T Kunick, C Meijer, L Sausville, EA
Citation: Dw. Zaharevitz et al., Discovery and initial characterization of the paullones, a novel class of small-molecule inhibitors of cyclin-dependent kinases, CANCER RES, 59(11), 1999, pp. 2566-2569
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