Structure-based design of 3-aryl-6-amino-triazolo[4,3-b]pyridazine inhibitors of Pim-1 kinase by Grey, Ron, Pierce, Albert C., Bemis, Guy W., Jacobs, Marc D., Moody, Cameron Stuver, Jajoo, Rahul, Mohal, Narinder, Green, Jeremy

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Kinase-likeness and Kinase-Privileged Fragments: Toward Virtual Polypharmacology by Aronov, Alex M, McClain, Brian, Moody, Cameron Stuver, Murcko, Mark A

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Design, synthesis and biological evaluation of potent NAD+-dependent DNA ligase inhibitors as potential antibacterial agents. Part II: 4-amino-pyrido[2,3-d]pyrimidin-5(8H)-ones by TIANSHENG WANG, DUNCAN, Leonard, CHARIFSON, Paul S, WENXIN GU, O'DOWD, Hardwin, YUNYI WEI, PEROLA, Emanuele, PARSONS, Jonathan, GROSS, Christian H, CAMERON STUVER MOODY, RYAN ARENDS, S. J

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Design, Synthesis, and Evaluation of a Novel Dual Fms-Like Tyrosine Kinase 3/Stem Cell Factor Receptor (FLT3/c-KIT) Inhibitor for the Treatment of Acute Myelogenous Leukemia by Davies, Robert J, Pierce, Albert C, Forster, Cornelia, Grey, Ron, Xu, Jinwang, Arnost, Michael, Choquette, Deborah, Galullo, Vincent, Tian, Shi-Kai, Henkel, Greg, Chen, Guanjing, Heidary, David K, Ma, Joanne, Stuver-Moody, Cameron, Namchuk, Mark

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4-(Benzimidazol-2-yl)-1,2,5-oxadiazol-3-ylamine derivatives: Potent and selective p70S6 kinase inhibitors by Bandarage, Upul, Hare, Brian, Parsons, Jonathan, Pham, Ly, Marhefka, Craig, Bemis, Guy, Tang, Qing, Moody, Cameron Stuver, Rodems, Steve, Shah, Sundeep, Adams, Chris, Bravo, Jose, Charonnet, Emmanuelle, Savic, Vladimir, Come, Jon H., Green, Jeremy

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Docking Study Yields Four Novel Inhibitors of the Protooncogene Pim-1 Kinase by Pierce, Albert C, Jacobs, Marc, Stuver-Moody, Cameron

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Characterization of pharmacological efficacy of VX-148, a new, potent immunosuppressive inosine 5'-monophosphate dehydrogenase inhibitor by Jain, Jugnu, Almquist, Susan J, Heiser, Angela D, Shlyakhter, Dina, Leon, Eduardo, Memmott, Christine, Moody, Cameron Stuver, Nimmesgern, Elmar, Decker, Caroline

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Multisystem Analysis of Mycobacterium tuberculosis Reveals Kinase-Dependent Remodeling of the Pathogen-Environment Interface by Carette, Xavier, Platig, John, Young, David C, Helmel, Michaela, Young, Albert T, Wang, Zhe, Potluri, Lakshmi-Prasad, Moody, Cameron Stuver, Zeng, Jumei, Prisic, Sladjana, Paulson, Joseph N, Muntel, Jan, Madduri, Ashoka V R, Velarde, Jorge, Mayfield, Jacob A, Locher, Christopher, Wang, Tiansheng, Quackenbush, John, Rhee, Kyu Y, Moody, D Branch, Steen, Hanno, Husson, Robert N

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Mtb PKNA/PKNB Dual Inhibition Provides Selectivity Advantages for Inhibitor Design To Minimize Host Kinase Interactions by Wang, Tiansheng, Bemis, Guy, Hanzelka, Brian, Zuccola, Harmon, Wynn, Michael, Moody, Cameron Stuver, Green, Jeremy, Locher, Christopher, Liu, Aixiang, Gao, Hongwu, Xu, Yuzhou, Wang, Shaohui, Wang, Jie, Bennani, Youssef L, Thomson, John A, Müh, Ute

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Design, synthesis and biological evaluation of potent NAD+-dependent DNA ligase inhibitors as potential antibacterial agents. Part 2: 4-Amino-pyrido[2,3-d]pyrimidin-5(8H)-ones by Wang, Tiansheng, Duncan, Leonard, Gu, Wenxin, O’Dowd, Hardwin, Wei, Yunyi, Perola, Emanuele, Parsons, Jonathan, Gross, Christian H., Moody, Cameron Stuver, Ryan Arends, S.J., Charifson, Paul S.

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Multisystem Analysis of italic toggle="yes">Mycobacterium tuberculosis /italic> Reveals Kinase-Dependent Remodeling of the Pathogen-Environment Interface by Xavier Carette, John Platig, David C. Young, Michaela Helmel, Albert T. Young, Zhe Wang, Lakshmi-Prasad Potluri, Cameron Stuver Moody, Jumei Zeng, Sladjana Prisic, Joseph N. Paulson, Jan Muntel, Ashoka V. R. Madduri, Jorge Velarde, Jacob A. Mayfield, Christopher Locher, Tiansheng Wang, John Quackenbush, Kyu Y. Rhee, D. Branch Moody, Hanno Steen, Robert N. Husson

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Characterization of Pharmacological Efficacy of VX-148, a New, Potent Immunosuppressive Inosine 5′-Monophosphate Dehydrogenase Inhibitor by Jugnu Jain, Susan J. Almquist, Angela D. Heiser, Dina Shlyakhter, Eduardo Leon, Christine Memmott, Cameron Stuver Moody, Elmar Nimmesgern, Caroline Decker

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