Nonsteroidal inhibitors of human type I steroid 5-.alpha.-reductase von Jones, Charles D, Audia, James E, Lawhorn, David E, McQuaid, Loretta A, Neubauer, Blake L, Pike, Andrew J, Pennington, Pamela A, Stamm, Nancy B, Toomey, Richard E, Hirsch, Kenneth S

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3-Phenyl-4-hydroxyquinolin-2(1H)-ones: potent and selective antagonists at the strychnine-insensitive glycine site on the N-methyl-D-aspartate receptor complex von McQuaid, Loretta A, Smith, Edward C. R, Lodge, David, Pralong, Etienne, Wikel, James H, Calligaro, David O, O'Malley, Patrick J

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Synthesis and excitatory amino acid pharmacology of a series of heterocyclic-fused quinoxalinones and quinazolinones von McQuaid, Loretta A, Smith, Edward C. R, South, Kimberly K, Mitch, Charles H, Schoepp, Darryle D, True, Rebecca A, Calligaro, David O, O'Malley, Patrick J, Lodge, David, Ornstein, Paul L

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Total synthesis of (.+-.)-methyl shikimate and (.+-.)-3-phosphoshikimic acid von Bartlett, Paul A, McQuaid, Loretta A

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An enantioselective synthesis of D-(-)- and L-(+)-2-amino-3-phosphonopropanoic acid von Smith, Edward C. R, McQuaid, Loretta A, Paschal, Jonathan W, DeHoniesto, Juel

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5,7-Dichlorokynurenic acid, a potent and selective competitive antagonist of the glycine site on NMDA receptors von McNamara, Dennis, Smith, Edward C.R., Calligaro, David O., O'Malley, Patrick J., McQuaid, Loretta A., Dingledine, Raymond

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Substituted 5-amino-4,5,6,7-tetrahydroindazoles as partial ergoline structures with dopaminergic activity von McQuaid, Loretta A, Latz, Jane E, Clemens, James A, Fuller, Ray W, Wong, David T, Mason, Norman R

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Stereoselectivity and mode of inhibition of phosphoinositide-coupled excitatory amino acid receptors by 2-amino-3-phosphonopropionic acid von SCHOEPP, D. D, JOHNSON, B. G, SMITH, E. C. R, MCQUAID, L. A

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LY191704: A Selective, Nonsteroidal Inhibitor of Human Steroid 5α- Reductase Type 1 von Hirsch, Kenneth S., Jones, Charles D., Audia, James E., Andersson, Stefan, McQuaid, Loretta, Stamm, Nancy B., Neubauer, Blake L., Pennington, Pam, Toomey, Richard E., Russell, David W.

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Synthesis and 5α-reductase inhibitory activity of 8-substituted benzo[ƒ]quinolinones derived from palladium mediated coupling reactions von Smith, Edward C.R., McQuaid, Loretta A., Goode, Robin L., McNulty, Ann M., Neubauer, Blake Lee, Rocco, Vincent P., Audia, James E.

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LY191704 inhibits type I steroid 5α-reductase in human scalp von NEUBAUER, B. L, GRAY, H. M, TINDALL, D. J, TOOMEY, R. E, YAO, R. C, AUDIA, J. E, HANKE, C. W, HIRSCH, K. S, HSIAO, K. C, JONES, C. D, KUMAR, M. V, LAWHORN, D. E, LINDZEY, J, MCQUAID, L

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Structure-activity relationships of a series of glycine antagonists related to 5,7-dichlorokynurenic acid and 3-(2-carboxy-6-chloroindol-3-yl)acetic acid von Smith, Edward C.R., McQuaid, Loretta A., Calligaro, David O., O'Malley, Patrick J.

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Creation of a Knowledge-Based System to Accelerate Drug Development von Hynes, Martin D., Getzin, Scott A., McQuaid, Loretta, Seward, Catherine M., Miller, Nicholas L., Field-Perez, Rebecca R.

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QSAR study of benzoquinolinones as inhibitors of human type 1 5-α-reductase von Wikel, James H., Bemis, Kerry G., Audia, James E., McQuaid, Loretta A., Jones, Charles D., Pennington, Pamela A., Lawhorn, David E., Hirsch, Kenneth R., Stamm, Nancy B.

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5 .ALPHA.-REDUCTASE INHIBITORS von MCQUAID, LORETTA AMES, NEUBAUER, BLAKE LEE, HAEHL, KEVIN LEE, WEPSIEC, JAMES PATRICK, ROCCO, VINCENT PATRICK, AUDIA, JAMES EDMUND, KRESS, THOMAS JOSEPH

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Benzo (f) quinolinones as 5-alpha-reductase inhibitors von MCQUAID, LORETTA AMES, WEIGEL, LELAND OTTO, HIRSCH, KENNETH STEVEN, JONES, CHARLES DAVID, LAWHORN, DAVID ERNEST, AUDIA, JAMES EDMUND

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5,6,7,8,9,10-hexahydro-8-hydroxy-5,8-dimethyl-5,9- methanobenzocyclooctan-11-one derivatives and process for preparing them von MCQUAID,LORETTA AMES, LAWHORN,DAVID ERNEST, JONES,CHARLES DAVID, WEIGEL,LELAND OTTO, HIRSCH,KENNETH STEVEN, AUDIA,JAMES EDMUND

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Benzo(f)quinolinone als 5-Alpha-reductase Inhibitoren von MCQUAID, LORETTA AMES, WEIGEL, LELAND OTTO, HIRSCH, KENNETH STEVEN, JONES, CHARLES DAVID, LAWHORN, DAVID ERNEST, AUDIA, JAMES EDMUND

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Benzo ÄFÜ quinolinnones von LAWHORN DAVID ERNEST, AUDIA JAMES EDMUND, JONES CHARLES DAVID, MCQUAID LORETTA AMES, HIRSCH KENNETH STEVEN

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Benzo(f)quinolinones as 5-alpha-reductase inhibitors von MCQUAID, LORETTA AMES, WEIGEL, LELAND OTTO, HIRSCH, KENNETH STEVEN, JONES, CHARLES DAVID, LAWHORN, DAVID ERNEST, AUDIA, JAMES EDMUND

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