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LXH254, a potent and selective ARAF-sparing inhibitor of BRAF and CRAF for the treatment of MAPK-driven tumors KA Monaco, S Delach, J Yuan, Y Mishina, P Fordjour, E Labrot, D McKay, ... Clinical cancer research 27 (7), 2061-2073, 2021 | 61 | 2021 |
Novel pyrazinone mono-amides as potent and reversible caspase-3 inhibitors Y Han, A Giroux, J Colucci, CI Bayly, DJ Mckay, S Roy, S Xanthoudakis, ... Bioorganic & medicinal chemistry letters 15 (4), 1173-1180, 2005 | 54 | 2005 |
β-Substituted cyclohexanecarboxamide: a nonpeptidic framework for the design of potent inhibitors of cathepsin K SN Crane, WC Black, JT Palmer, DE Davis, E Setti, J Robichaud, ... Journal of medicinal chemistry 49 (3), 1066-1079, 2006 | 47 | 2006 |
Discovery of novel aspartyl ketone dipeptides as potent and selective caspase-3 inhibitors Y Han, A Giroux, EL Grimm, R Aspiotis, S Francoeur, CI Bayly, DJ Mckay, ... Bioorganic & medicinal chemistry letters 14 (3), 805-808, 2004 | 45 | 2004 |
Could AlphaFold revolutionize chemical therapeutics? AB Tong, JD Burch, D McKay, C Bustamante, MA Crackower, H Wu Nature structural & molecular biology 28 (10), 771-772, 2021 | 43 | 2021 |
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