Discovery of a Novel 2,6-Disubstituted Glucosamine Series of Potent and Selective Hexokinase 2 Inhibitors von Lin, Hong, Zeng, Jin, Xie, Ren, Schulz, Mark J, Tedesco, Rosanna, Qu, Junya, Erhard, Karl F, Mack, James F, Raha, Kaushik, Rendina, Alan R, Szewczuk, Lawrence M, Kratz, Patricia M, Jurewicz, Anthony J, Cecconie, Ted, Martens, Stan, McDevitt, Patrick J, Martin, John D, Chen, Stephenie B, Jiang, Yong, Nickels, Leng, Schwartz, Benjamin J, Smallwood, Angela, Zhao, Baoguang, Campobasso, Nino, Qian, Yanqiu, Briand, Jacques, Rominger, Cynthia M, Oleykowski, Catherine, Hardwicke, Mary Ann, Luengo, Juan I

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Structural Basis for Chk1 Inhibition by UCN-01 von Zhao, Baoguang, Bower, Michael J, McDevitt, Patrick J, Zhao, Huizhen, Davis, Stephen T, Johanson, Kyung O, Green, Susan M, Concha, Nestor O, Zhou, Bin-Bing S

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Measuring the performance of green investment portfolios for zero-carbon environment: a comparative analysis of digital finance and asset-backed securities von Lei, Yaokai, Bao, Yujing, Zhao, Baoguang

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Design and synthesis of orally bioavailable serum and glucocorticoid-regulated kinase 1 (SGK1) inhibitors von Hammond, Marlys, Washburn, David G., Hoang, Tram H., Manns, Sharada, Frazee, James S., Nakamura, Hiroko, Patterson, Jaclyn R., Trizna, Walter, Wu, Charlene, Azzarano, Leonard M., Nagilla, Rakesh, Nord, Melanie, Trejo, Rebecca, Head, Martha S., Zhao, Baoguang, Smallwood, Angela M., Hightower, Kendra, Laping, Nicholas J., Schnackenberg, Christine G., Thompson, Scott K.

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Inhibition of Chk1 by the G2 DNA damage checkpoint inhibitor isogranulatimide von Jiang, Xiuxian, Zhao, Baoguang, Britton, Robert, Lim, Lynette Y, Leong, Dan, Sanghera, Jasbinder S, Zhou, Bin-Bing S, Piers, Edward, Andersen, Raymond J, Roberge, Michel

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Nurturing knowledge absorption in the organizations: examining the role of transformational leadership, learning climate, and proactive personality von Lei, YaoKai, Zhao, BaoGuang, An, LiJie

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Design, synthesis and selection of DNA-encoded small-molecule libraries von Morgan, Barry A, Clark, Matthew A, Acharya, Raksha A, Arico-Muendel, Christopher C, Belyanskaya, Svetlana L, Benjamin, Dennis R, Carlson, Neil R, Centrella, Paolo A, Chiu, Cynthia H, Creaser, Steffen P, Cuozzo, John W, Davie, Christopher P, Ding, Yun, Franklin, G Joseph, Franzen, Kurt D, Gefter, Malcolm L, Hale, Steven P, Hansen, Nils J V, Israel, David I, Jiang, Jinwei, Kavarana, Malcolm J, Kelley, Michael S, Kollmann, Christopher S, Li, Fan, Lind, Kenneth, Mataruse, Sibongile, Medeiros, Patricia F, Messer, Jeffrey A, Myers, Paul, O'Keefe, Heather, Oliff, Matthew C, Rise, Cecil E, Satz, Alexander L, Skinner, Steven R, Svendsen, Jennifer L, Tang, Lujia, van Vloten, Kurt, Wagner, Richard W, Yao, Gang, Zhao, Baoguang

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N-Phenyl- N-purin-6-yl ureas: The design and synthesis of p38α MAP kinase inhibitors von Wan, Zehong, Boehm, Jeffrey C., Bower, Michael J., Kassis, Shouki, Lee, John C., Zhao, Baoguang, Adams, Jerry L.

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Modulation of kinase‐inhibitor interactions by auxiliary protein binding: Crystallography studies on Aurora A interactions with VX‐680 and with TPX2 von Zhao, Baoguang, Smallwood, Angela, Yang, Jingsong, Koretke, Kristin, Nurse, Kelvin, Calamari, Amy, Kirkpatrick, Robert B., Lai, Zhihong

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Cyclic Ketone Inhibitors of the Cysteine Protease Cathepsin K von Marquis, Robert W, Ru, Yu, Zeng, Jin, Trout, Robert E. Lee, LoCastro, Stephen M, Gribble, Andrew D, Witherington, Jason, Fenwick, Ashley E, Garnier, Benedicte, Tomaszek, Thaddeus, Tew, David, Hemling, Mark E, Quinn, Chad J, Smith, Ward W, Zhao, Baoguang, McQueney, Michael S, Janson, Cheryl A, D'Alessio, Karla, Veber, Daniel F

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Use of Papain as a Model for the Structure-Based Design of Cathepsin K Inhibitors:  Crystal Structures of Two Papain−Inhibitor Complexes Demonstrate Binding to S‘-Subsites von LaLonde, Judith M, Zhao, Baoguang, Smith, Ward W, Janson, Cheryl A, DesJarlais, Renee L, Tomaszek, Thaddeus A, Carr, Thomas J, Thompson, Scott K, Oh, Hye-Ja, Yamashita, Dennis S, Veber, Daniel F, Abdel-Meguid, Sherin S

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Conformationally Constrained 1,3-Diamino Ketones:  A Series of Potent Inhibitors of the Cysteine Protease Cathepsin K von Marquis, Robert W, Yamashita, Dennis S, Ru, Yu, LoCastro, Stephen M, Oh, Hye-Ja, Erhard, Karl F, DesJarlais, Renee L, Head, Martha S, Smith, Ward W, Zhao, Baoguang, Janson, Cheryl A, Abdel-Meguid, Sherin S, Tomaszek, Thaddeus A, Levy, Mark A, Veber, Daniel F

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The Amino-Acid Substituents of Dipeptide Substrates of Cathepsin C Can Determine the Rate-Limiting Steps of Catalysis von Rubach, Jon K, Cui, Guanglei, Schneck, Jessica L, Taylor, Amy N, Zhao, Baoguang, Smallwood, Angela, Nevins, Neysa, Wisnoski, David, Thrall, Sara H, Meek, Thomas D

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Inhibition of human immunodeficiency virus-1 protease by a C2-symmetric phosphinate. Synthesis and crystallographic analysis von Abdel-Meguid, Sherin S, Zhao, Baoguang, Murthy, Krishna H. M, Winborne, Evon, Choi, Joong Kwon, DesJarlais, Renee L, Minnich, Michael D, Culp, Jeffrey S, Debouck, Christine

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Human Immunodeficiency Virus Protease Ligand Specificity Conferred by Residues Outside of the Active Site Cavity von Hoog, Susan S, Towler, Eric M, Zhao, Baoguang, Doyle, Michael L, Debouck, Christine, Abdel-Meguid, Sherin S

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Rational Design, Synthesis, and Crystallographic Analysis of a Hydroxyethylene-Based HIV-1 Protease Inhibitor Containing a Heterocyclic P1'-P2' Amide Bond Isostere von Thompson, Scott K, Murthy, Krishna H. M, Zhao, Baoguang, Winborne, Evon, Green, David W, Fisher, Seth M, DesJarlais, Renee L, Tomaszek, Thaddeus A. Jr, Meek, Thomas D

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Crystal structure of the kinase domain of serum and glucocorticoid‐regulated kinase 1 in complex with AMP–PNP von Zhao, Baoguang, Lehr, Ruth, Smallwood, Angela M., Ho, Thau F., Maley, Kathleen, Randall, Tanya, Head, Martha S., Koretke, Kristin K., Schnackenberg, Christine G.

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Structure-Based Design of Cathepsin K Inhibitors Containing a Benzyloxy-Substituted Benzoyl Peptidomimetic von Thompson, Scott K, Smith, Ward W, Zhao, Baoguang, Halbert, Stacie M, Tomaszek, Thaddeus A, Tew, David G, Levy, Mark A, Janson, Cheryl A, D‘Alessio, Karla J, McQueney, Michael S, Kurdyla, Jeff, Jones, Christopher S, DesJarlais, Renee L, Abdel-Meguid, Sherin S, Veber, Daniel F

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Discovery of Novel Cyanamide-Based Inhibitors of Cathepsin C von Lainé, Dramane, Palovich, Michael, McCleland, Brent, Petitjean, Emilie, Delhom, Isabelle, Xie, Haibo, Deng, Jianghe, Lin, Guoliang, Davis, Roderick, Jolit, Anais, Nevins, Neysa, Zhao, Baoguang, Villa, Jim, Schneck, Jessica, McDevitt, Patrick, Midgett, Robert, Kmett, Casey, Umbrecht, Sandra, Peck, Brian, Davis, Alicia Bacon, Bettoun, David

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A Check on Rational Drug Design: Crystal Structure of a Complex of Human Immunodeficiency Virus Type 1 Protease with a Novel .gamma.-Turn Mimetic Inhibitor von Hoog, Susan S, Zhao, Baoguang, Winborne, Evon, Fisher, Seth, Green, David W, DesJarlais, Renee L, Newlander, Kenneth A, Callahan, James F, Abdel-Meguid, Sherin S, Moore, Michael L, Huffman, William F

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