SB 209670, a Rationally Designed Potent Nonpeptide Endothelin Receptor Antagonist von Ohlstein, Eliot H., Nambi, Ponnal, Douglas, Stephen A., Edwards, Richard M., Gellai, Miklos, Lago, Amparo, Leer, Jack D., Cousins, Russell D., Gao, Aiming, Frazee, James S., Peishoff, Catherine E., Bean, John W., Eggleston, Drake S., Elshourbagy, Nabil A., Kumar, Chandrika, Lee, Jonathan A., Yue, Tian-Li, Louden, Calvert, Brooks, David P., Weinstock, Joseph, Feuerstein, Giora, Poste, George, Ruffolo, Robert R., Gleason, John G., Elliott, John D.

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Orally Active and Potent Inhibitors of γ-Aminobutyric Acid Uptake von Ali, Fadia E, Bondinell, William E, Dandridge, Penelope A, Frazee, James S, Garvey, Eleanor, Girard, Gerald R, Kaiser, Carl, Ku, Thomas W, Lafferty, John J, Moonsammy, George I, Oh, Hye-Ja, Rush, Julia A, Setler, Paulette E, Stringer, Orum D, Venslavsky, Joseph W, Volpe, Beth W, Yunger, Libby M, Zirkle, Charles L

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High-affinity leukotriene receptor antagonists. Synthesis and pharmacological characterization of 2-hydroxy-3-[(2-carboxyethyl)thio]-3-[2-(8-phenyloctyl)phenyl]propanoic acid von Gleason, John G, Hall, Ralph F, Perchonock, Carl D, Erhard, Karl F, Frazee, James S, Ku, Thomas W, Kondrad, Karen, McCarthy, Mary E, Mong, Seymour

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Substituted 1-benzylimidazole-2-thiols as potent and orally active inhibitors of dopamine .beta.-hydroxylase von Kruse, Lawrence I, Kaiser, Carl, DeWolf, Walter E, Frazee, James S, Erickson, Robert W, Ezekiel, Mildred, Ohlstein, Eliot H, Ruffolo, Robert R, Berkowitz, Barry A

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Some benzyl-substituted imidazoles, triazoles, tetrazoles, pyridinethiones, and structural relatives as multisubstrate inhibitors of dopamine .beta.-hydroxylase. 4. Structure-activ... von Kruse, Lawrence I, Kaiser, Carl, DeWolf, Walter E, Finkelstein, Joseph A, Frazee, James S, Hilbert, Eileen L, Ross, Stephen T, Flaim, Kathryn E, Sawyer, John L

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3-Phenyl-5-quinolinemethanol antimalarials von Makriyannis, Alexandros, Wilson, James W, Frazee, James S

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Synthesis and antiviral activity of a novel class of HIV-1 protease inhibitors containing a heterocyclic P 1′-P 2′ amide bond isostere von Thompson, Scott K., Eppley, Alecia M., Frazee, James S., Darcy, Michael G., Lum, Robert T., Tomaszek, Thaddeus A., Ivanoff, Lucinda A., Morris, Jane F., Sternberg, Edmund J., Lambert, Dennis M., Fernandez, Annabellee V., Petteway, Stephen R., Meek, Thomas D, Metcalf, Brian W., Gleason, John G.

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Adrenerigic agents. 7.1 Synthesis and beta-adrenergic agonist activity of several 2-pyridylethanolamines von Jen, T, Frazee, J S, Schwartz, M S, Kaiser, C

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Multisubstrate inhibitors of dopamine β-hydroxylase. II: Structure-activity relationships at the phenethylamine binding site von KRUSE, L. I, KAISER, C, EZEKIEL, M, OHLSTEIN, E. H, BERKOWITZ, B. A, DEWOLF, W. E. JR, FRAZEE, J. S, ROSS, S. T, WAWRO, J, WISE, M, FLAIM, K. E, SAWYER, J. L, ERICKSON, R. W

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Multisubstrate inhibitors of dopamine β-hydroxylase. I: Some 1-phenyl and 1-phenyl-bridged derivatives of imidazole-2-thione von KRUSE, L. I, KAISER, C, DEWOLF, W. E. JR, FRAZEE, J. S, GARVEY, E, HILBERT, E. L, FAULKNER, W. A, FLAIM, K. E, SAWYER, J. L, BERKOWITZ, B. A

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Adrenergic agents. 8.1 Synthesis and beta-adrenergic agonist activity of some 3-tert-butylamino-2-(substituted phenyl)-1-propanols von Jen, T, Frazee, J S, Schwartz, M S, Erhard, K F, Kaiser, C

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Adrenergic agents. 8. Synthesis and .beta.-adrenergic agonist activity of some 3-tert-butylamino-2-(substituted phenyl)-1-propanols von Jen, Timothy, Frazee, James S, Schwartz, Mark S, Erhard, Karl F, Kaiser, Carl, Colella, Donald F, Wardell, Joe R

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AUTOMATIC RANGEFINDER ELECTRONIC CIRCUITRY von FRAZEE J,US, MURPHY H,US

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Three Fatal Intoxications Due to Methylone von Pearson, Julia M., Hargraves, Tiffanie L., Hair, Laura S., Massucci, Charles J., Clinton Frazee, C., Garg, Uttam, Pietak, B. Robert

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