Metastin (KiSS-1) Mimetics Identified from Peptide Structure−Activity Relationship-Derived Pharmacophores and Directed Small Molecule Database Screening von Orsini, Michael J, Klein, Mark A, Beavers, Mary Pat, Connolly, Peter J, Middleton, Steven A, Mayo, Kevin H

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Antibody modeling assessment von Almagro, Juan C., Beavers, Mary Pat, Hernandez-Guzman, Francisco, Maier, Johannes, Shaulsky, Jodi, Butenhof, Kenneth, Labute, Paul, Thorsteinson, Nels, Kelly, Kenneth, Teplyakov, Alexey, Luo, Jinquan, Sweet, Raymond, Gilliland, Gary L.

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Identification and characterization of 3-substituted pyrazolyl esters as alternate substrates for cathepsin B: The confounding effects of DTT and cysteine in biological assays von Myers, Michael C., Napper, Andrew D., Motlekar, Nuzhat, Shah, Parag P., Chiu, Chun-Hao, Beavers, Mary Pat, Diamond, Scott L., Huryn, Donna M., Smith, Amos B.

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Small-molecule inhibitors of integrin α₂β₁ that prevent pathological thrombus formation via an allosteric mechanism von Miller, Meredith W, Basra, Sandeep, Kulp, Daniel W, Billings, Paul C, Choi, Sungwook, Beavers, Mary Pat, McCarty, Owen J.T, Zou, Zhiying, Kahn, Mark L, Bennett, Joel S, DeGrado, William F

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The Total Synthesis of Roquefortine C and a Rationale for the Thermodynamic Stability of Isoroquefortine C over Roquefortine C von Shangguan, Ning, Hehre, Warren J, Ohlinger, William S, Beavers, Mary Pat, Joullié, Madeleine M

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Kinetic Characterization and Molecular Docking of a Novel, Potent, and Selective Slow-Binding Inhibitor of Human Cathepsin L von Shah, Parag P, Myers, Michael C, Beavers, Mary Pat, Purvis, Jeremy E, Jing, Huiyan, Grieser, Heather J, Sharlow, Elizabeth R, Napper, Andrew D, Huryn, Donna M, Cooperman, Barry S, Smith, 3rd, Amos B, Diamond, Scott L

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Heteroaryl- O-glucosides as novel sodium glucose co-transporter 2 inhibitors. Part 1 von Zhang, Xiaoyan, Urbanski, Maud, Patel, Mona, Zeck, Roxanne E., Cox, Geoffrey G., Bian, Haiyan, Conway, Bruce R., Pat Beavers, Mary, Rybczynski, Philip J., Demarest, Keith T.

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The Nociceptin Pharmacophore Site for Opioid Receptor Binding Derived from the NMR Structure and Bioactivity Relationships von Orsini, Michael J, Nesmelova, Irina, Young, Helen C, Hargittai, Balazs, Beavers, Mary Pat, Liu, Jingchun, Connolly, Peter J, Middleton, Steven A, Mayo, Kevin H

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Synthesis and evaluation of 3-anilino-quinoxalinones as glycogen phosphorylase inhibitors von Dudash, Joseph, Zhang, Yongzheng, Moore, John B., Look, Richard, Liang, Yin, Beavers, Mary Pat, Conway, Bruce R., Rybczynski, Philip J., Demarest, Keith T.

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Synthesis and Discovery of Macrocyclic Polyoxygenated Bis-7-azaindolylmaleimides as a Novel Series of Potent and Highly Selective Glycogen Synthase Kinase-3β Inhibitors von Kuo, Gee-Hong, Prouty, Catherine, DeAngelis, Alan, Shen, Lan, O'Neill, David J, Shah, Chandra, Connolly, Peter J, Murray, William V, Conway, Bruce R, Cheung, Peter, Westover, Lori, Xu, Jun Z, Look, Richard A, Demarest, Keith T, Emanuel, Stuart, Middleton, Steven A, Jolliffe, Linda, Beavers, Mary Pat, Chen, Xin

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Molecular Docking of Cathepsin L Inhibitors in the Binding Site of Papain von Beavers, Mary Pat, Myers, Michael C, Shah, Parag P, Purvis, Jeremy E, Diamond, Scott L, Cooperman, Barry S, Huryn, Donna M, Smith, Amos B

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Structure-based combinatorial library design: methodologies and applications von Beavers, Mary Pat, Chen, Xin

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Nonpeptidic, Noncovalent Inhibitors of the Cysteine Protease Cathepsin S von Thurmond, Robin L, Beavers, Mary Pat, Cai, Hui, Meduna, Steven P, Gustin, Darin J, Sun, Siquan, Almond, Harold J, Karlsson, Lars, Edwards, James P

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Design, synthesis, and evaluation of inhibitors of cathepsin L: Exploiting a unique thiocarbazate chemotype von Myers, Michael C., Shah, Parag P., Beavers, Mary Pat, Napper, Andrew D., Diamond, Scott L., Smith, Amos B., Huryn, Donna M.

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Indole-glucosides as novel sodium glucose co-transporter 2 (SGLT2) inhibitors. Part 2 von Zhang, Xiaoyan, Urbanski, Maud, Patel, Mona, Cox, Geoffrey G., Zeck, Roxanne E., Bian, Haiyan, Conway, Bruce R., Beavers, Mary Pat, Rybczynski, Philip J., Demarest, Keith T.

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Molecular Docking of Cathepsin L Inhibitors in the Binding Site of Papain von Beavers, Mary Pat, Myers, Michael C, Shah, Parag P, Purvis, Jeremy E, Diamond, Scott L, Cooperman, Barry S, Huryn, Donna M, Smith, Amos B

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Small-molecule inhibitors of integrin [alpha]^sub 2^[beta]^sub 1^ that prevent pathological thrombus formation via an allosteric mechanism von Miller, Meredith W, Basra, Sandeep, Kulp, Daniel W, Billings, Paul C, Choi, Sungwook, Beavers, Mary Pat, McCarty, Owen J T, Zou, Zhiying, Kahn, Mark L, Bennett, Joel S, DeGrado, William F

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Small-molecule inhibitors of integrin α 2 β 1 that prevent pathological thrombus formation via an allosteric mechanism von Miller, Meredith W., Basra, Sandeep, Kulp, Daniel W., Billings, Paul C., Choi, Sungwook, Beavers, Mary Pat, McCarty, Owen J. T., Zou, Zhiying, Kahn, Mark L., Bennett, Joel S., DeGrado, William F.

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Small-molecule inhibitors of integrin α₂β₁ that prevent pathological thrombus formation via an allosteric mechanism von Miller, Meredith W, Basra, Sandeep, Kulp, Daniel W, Billings, Paul C, Choi, Sungwook, Beavers, Mary Pat, McCarty, Owen J.T, Zou, Zhiying, Kahn, Mark L, Bennett, Joel S, DeGrado, William F

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Synthesis and biological evaluation of novel macrocyclic bis-7-azaindolylmaleimides as potent and highly selective glycogen synthase kinase-3β (GSK-3β) inhibitors von SHEN, Lan, PROUTY, Catherine, DEMAREST, Keith T, KUO, Gee-Hong, CONWAY, Bruce R, WESTOVER, Lori, XU, Jun Z, LOOK, Richard A, XIN CHEN, BEAVERS, Mary Pat, ROBERTS, Jerry, MURRAY, William V

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