Viracept (Nelfinavir Mesylate, AG1343):  A Potent, Orally Bioavailable Inhibitor of HIV-1 Protease von Kaldor, Stephen W, Kalish, Vincent J, Davies, Jay F, Shetty, Bhasker V, Fritz, James E, Appelt, Krzysztof, Burgess, Jeffrey A, Campanale, Kristina M, Chirgadze, Nickolay Y, Clawson, David K, Dressman, Bruce A, Hatch, Steven D, Khalil, Deborah A, Kosa, Maha B, Lubbehusen, Penny P, Muesing, Mark A, Patick, Amy K, Reich, Siegfried H, Su, Kenneth S, Tatlock, John H

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Crystal structures of human calcineurin and the human FKBP12–FK506–calcineurin complex von Kissinger, Charles R., Parge, Hans E., Knighton, Daniel R., Lewis, Cristina T., Pelletier, Laura A., Tempczyk, Anna, Kalish, Vincent J., Tucker, Kathleen D., Showalter, Richard E., Moomaw, Ellen W., Gastinel, Louis N., Habuka, Noriyuki, Chen, Xinghai, Maldonado, Fausto, Barker, John E., Bacquet, Russell, Villafranca, J. Ernest

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Synthesis of substituted 5[ H]phenanthridin-6-ones as potent poly(ADP-ribose)polymerase-1 (PARP1) inhibitors von Li, Jia-He, Serdyuk, Larisa, Ferraris, Dana V., Xiao, Ge, Tays, Kevin L., Kletzly, Paul W., Li, Weixing, Lautar, Susan, Zhang, Jie, Kalish, Vincent J.

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Synthesis and structure-activity relationships of acyclic .omega. chain conjugated diene analogs of enisoprost von Collins, P. W, Shone, R. L, Perkins, W. E, Gasiecki, A. F, Kalish, V. J, Kramer, S. W, Bianchi, R. G

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Structure-Based Design of Novel, Urea-Containing FKBP12 Inhibitors von Dragovich, Peter S, Barker, John E, French, Judy, Imbacuan, Michael, Kalish, Vincent J, Kissinger, Charles R, Knighton, Daniel R, Lewis, Cristina T, Moomaw, Ellen W, Parge, Hans E, Pelletier, Laura A. K, Prins, Thomas J, Showalter, Richard E, Tatlock, John H, Tucker, Kathleen D, Villafranca, J. Ernest

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Design and synthesis of poly(ADP-ribose) polymerase-1 (PARP-1) inhibitors. part 4: Biological evaluation of imidazobenzodiazepines as potent PARP-1 inhibitors for treatment of isch... von Ferraris, Dana, Ficco, Rica Pargas, Dain, David, Ginski, Mark, Lautar, Susan, Lee-Wisdom, Kathy, Liang, Shi, Lin, Qian, Lu, May X.-C, Morgan, Lisa, Thomas, Bert, Williams, Lawrence R, Zhang, Jie, Zhou, Yinong, Kalish, Vincent J

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Approaches to the total synthesis of the antitumor antibiotic echinosporin von Kinsella, Mary A, Kalish, Vincent J, Weinreb, Steven M

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Structure–activity relationships within a series of caspase inhibitors. Part 2: Heterocyclic warheads von Ullman, Brett R., Aja, Teresa, Chen, Ning, Diaz, Jose-Luis, Gu, Xin, Herrmann, Julia, Kalish, Vincent J., Karanewsky, Donald S., Kodandapani, Lalitha, Krebs, Joseph J., Linton, Steven D., Meduna, Steven P., Nalley, Kip, Robinson, Edward D., Roggo, Silvio P., Sayers, Robert O., Schmitz, Albert, Ternansky, Robert J., Tomaselli, Kevin J., Wu, Joe C.

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Structure-activity relationships within a series of caspase inhibitors: Effect of leaving group modifications von ULLMAN, Brett R, AJA, Teresa, ROGGO, Silvio P, SAYERS, Robert O, SCHMITZ, Albert, TERNANSKY, Robert J, TOMASELLI, Kevin J, WU, Joe C, DECKWERTH, Thomas L, DIAZ, Jose-Luis, HERRMANN, Julia, KALISH, Vincent J, KARANEWSKY, Donald S, MEDUNA, Steven P, NALLEY, Kip, ROBINSON, Edward D

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Acyl dipeptides as reversible caspase inhibitors. Part 2: Further optimization von LINTON, Steven D, KARANEWSKY, Donald S, WU, Joe C, PHAM, Brian, KODANDAPANI, Lalitha, SMIDT, Robert, DIAZ, Jose-Luis, FRITZ, Lawrence C, VON KROSIGK, U, ROGGO, Silvio, SCHMITZ, Albert, TOMASELLI, Kevin J, TERNANSKY, Robert J, NING CHEN, GUO, Xian, JAHANGIRI, Kathy G, KALISH, Vincent J, MEDUNA, Steven P, ROBINSON, Edward D, ULLMAN, Brett R

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Improved Procedure for the Reduction of N-Acyloxazolidinones von Penning, Thomas D., Djuric, Stevan W., Haack, Richard A., Kalish, Vincent J., Miyashiro, Julie M., Rowell, Bruce W., Yu, Stella S.

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Structure-based drug design of nonpeptidic P 2 substituents for HIV-1 protease inhibitors von Kalish, Vincent J., Tatlock, John H., Davies, Jay F., Kaldor, Stephen W., Dressman, Bruce A., Reich, Siegfried, Pino, Mark, Nyugen, Dzuy, Appelt, Krzysztof, Musick, Linda, Wu, Bor-wen

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Double cyclization of aminophosphonoacetate derived β- hydroxyacids to bicyclic β-lactams von Huang, Nai Z., Kalish, Vincent J., Miller, Marvin J.

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Crystal structures of human calcineurin and the human FKBP-12-FK506-calcineurin complex von KISSINGER, C. R, PARGE, H. E, GASTINEL, L. N, HABUKA, N, XINGHAI CHEN, MALDONADO, F, BARKER, J. E, BACQUET, R, VILLAFRANCA, J. E, KNIGHTON, D. R, LEWIS, C. T, PELLETIER, L. A, TEMPCZYK, A, KALISH, V. J, TUCKER, K. D, SHOWALTER, R. E, MOOMAW, E. W

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An Improved Procedure for the Synthesis of Prostaglandin Analogues von Kalish, Vincent J., Shone, Robert L., Kramer, Steven W., Collins, Paul W., Babiak, Kevin A., McLaughlin, Kathleen T., Ng, John S.

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Systematic review and meta-analysis of steatosis as a risk factor in major hepatic resection von de Meijer, V. E., Kalish, B. T., Puder, M., IJzermans, J. N. M.

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Characterization of Few-Layer 1T′ MoTe2 by Polarization-Resolved Second Harmonic Generation and Raman Scattering von Beams, Ryan, Cançado, Luiz Gustavo, Krylyuk, Sergiy, Kalish, Irina, Kalanyan, Berç, Singh, Arunima K, Choudhary, Kamal, Bruma, Alina, Vora, Patrick M, Tavazza, Francesca, Davydov, Albert V, Stranick, Stephan J

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Tuning of the transverse magneto-optical Kerr effect in magneto-plasmonic crystals von Pohl, M, Kreilkamp, L E, Belotelov, V I, Akimov, I A, Kalish, A N, Khokhlov, N E, Yallapragada, V J, Gopal, A V, Nur-E-Alam, M, Vasiliev, M, Yakovlev, D R, Alameh, K, Zvezdin, A K, Bayer, M

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Probing the Optical Properties and Strain-Tuning of Ultrathin Mo1–xWxTe2 von Aslan, Ozgur Burak, Datye, Isha M., Mleczko, Michal J., Cheung, Karen Sze, Krylyuk, Sergiy, Bruma, Alina, Kalish, Irina, Davydov, Albert V., Pop, Eric, Heinz, Tony F.

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Rapid Wafer-Scale Growth of Polycrystalline 2H-MoS2 by Pulsed Metal–Organic Chemical Vapor Deposition von Kalanyan, Berc, Kimes, William A, Beams, Ryan, Stranick, Stephan J, Garratt, Elias, Kalish, Irina, Davydov, Albert V, Kanjolia, Ravindra K, Maslar, James E

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