Cyclic urea derivatives as potent NK1 selective antagonists von SHUE, Ho-Jane, XIAO CHEN, PIWINSKI, John J, DUFFY, Ruth A, LACHOWICZ, Jean E, COFFIN, Vicki L, FEI LIU, NOMEIR, Amin A, MORGAN, Cynthia A, VARTY, Geoffrey B, SHIH, Neng-Yang, BLYTHIN, David J, PALIWAL, Sunil, LING LIN, DANLIN GU, SCHWERDT, John H, SHAH, Sapna, REICHARD, Gregory A

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Synthesis of Racemic cis- and trans-3-Phenylazetidine-2-Carboxylic Acids as Conformationally Restricted Analogs of Phenylalanine von Blythin, David J, Green, Michael J, Lauzon, Mary Jane R, Shue, Ho-Jane

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Anti-allergy agents. 3. Angular tricyclic ether derivatives of the 1,8-naphthyridin-2(1H)-one ring system von Blythin, David J., Shue, Ho-Jane, Carlon, Emilie, Spitler, James, Kreutner, William

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Synthesis and NK1/NK2 Binding Activities of a Series of Diacyl-Substituted 2-Arylpiperazines von Blythin, David J., Chen, Xiao, Piwinski, John J., Shih, Neng-Yang, Shue, Ho-Jane, Anthes, John C., McPhail, Andrew T.

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Cyclic urea derivatives as potent NK 1 selective antagonists. Part II: Effects of fluoro and benzylic methyl substitutions von Shue, Ho-Jane, Chen, Xiao, Schwerdt, John H., Paliwal, Sunil, Blythin, David J., Lin, Ling, Gu, Danlin, Wang, Cheng, Reichard, Gregory A., Wang, Hongwu, Piwinski, John J., Duffy, Ruth A., Lachowicz, Jean E., Coffin, Vicki L., Nomeir, Amin A., Morgan, Cynthia A., Varty, Geoffrey B., Shih, Neng-Yang

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Cyclic urea derivatives as potent NK1 selective aantagonists. Part II: Effects of fluoro and benzylic methyl substitutions von SHUE, Ho-Jane, XIAO CHEN, PIWINSKI, John J, DULLY, Ruth A, LACHOWICZ, Jean E, COFFIN, Vicki L, NOMEIR, Amin A, MORGAN, Cynthia A, VARTY, Geoffrey B, SHIH, Neng-Yang, SCHWERDT, John H, PALIWAL, Sunil, BLYTHIN, David J, LING LIN, DANLIN GU, CHENG WANG, REICHARD, Gregory A, HONGWU WANG

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A new method for labelling 11β-hydroxy steroids: Synthesis of 18-2H-corticosteroids von Green, Michael J., Shue, Ho-Jane, Bartner, Peter, Morton, James B., Youngstrom, Richard E., Meinwald, Jerrold

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Cyclic urea derivatives as potent NK 1 selective antagonists von Shue, Ho-Jane, Chen, Xiao, Shih, Neng-Yang, Blythin, David J., Paliwal, Sunil, Lin, Ling, Gu, Danlin, Schwerdt, John H., Shah, Sapna, Reichard, Gregory A., Piwinski, John J., Duffy, Ruth A., Lachowicz, Jean E., Coffin, Vicki L., Liu, Fei, Nomeir, Amin A., Morgan, Cynthia A., Varty, Geoffrey B.

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Synthesis and NK 1/NK 2 binding activities of a series of diacyl-substituted 2-arylpiperazines von Blythin, David J., Chen, Xiao, Piwinski, John J., Shih, Neng-Yang, Shue, Ho-Jane, Anthes, John C., McPhail, Andrew T.

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Steroid spiro[2·4]heptan-4-ones: Products of the reaction between diphenylcyclopropylsulfonium ylide and steroid 4,6-diene-3-ones von Green, Michael J., Shue, Ho-Jane, McPhail, Andrew T., Miller, Richard W.

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Synthesis and structure-activity relationships in a novel series of topically active corticosteroids von Green, Michael J., Berkenkopf, Joseph, Fernandez, Xiomara, Monahan, Margaret, Shue, Ho-Jane, Tiberi, Robert L., Lutsky, Barry N.

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Forskolin: a convenient degradation to 14,15-dinor-8,13-epoxy-1α,6β,7β,9α-tetrahydroxylabd-12-en-11-one 7-acetate 1,9-carbonate via β-elimination of an aldoxime von SAKSENA, A. K, GREEN, M. J, SHUE, H.-J, WONG, J. K

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Recent advances in the structure-activity relationships of substituted corticosteroids von Green, Michael J., Bisarya, Satish C., Herzog, Hershel L., Rausser, Richard, Shapiro, Elliot L., Shue, Ho-Jane, Sutton, Betty, Tiberi, Robert L., Monahan, Margaret, Collins, Elliott J.

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A study of 3-amino-N-hydroxypropanesulfonamide derivatives as potential GABAB agonists and their fragmentation to 3-aminopropanesulfinic acid von Ho-Jane Shue, Xiao Chen, Blythin, David J., Carruthers, Nicholas I., Spitler, James M., Shing-Chun Wong, Chapman, Richard W., Rizzo, Charles, West, Robert, She, Hoyan S.

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Substituted morpholine-2S-acetic acid derivatives: Sch 50911 and related compounds as novel GABAB antagonists von Blythin, David J., Kuo, Shen-Chun, Shue, Ho-Jane, McPhail, Andrew T., Chapman, Richard W., Kreutner, William, Rizzo, Charles, She, Hoyan S., West, Robert

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Synthesis and resolution of β-(aminomethyl)-4-chlorobenzeneethanesulfinic acid a potent gaba B receptor ligand von Carruthers, Nicholas I., Spitler, James M., Shing-Chun Wong, Blythin, David J., Xiao Chen, Ho-Jane Shue, Mittelman, Stanley

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A study of 3-amino-N-hydroxypropanesulfonamide derivatives as potential GABA B agonists and their fragmentation to 3-aminopropanesulfinic acid von Ho-Jane Shue, Xiao Chen, Blythin, David J., Carruthers, Nicholas I., Spitler, James M., Shing-Chun Wong, Chapman, Richard W., Rizzo, Charles, West, Robert, She, Hoyan S.

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Maleate, tosylate, fumarate and oxalate salts of 5-(1-(S)-amino-2-hydroxyethyl)-N-[(2,4-difluorophenyl)-methy]-2-[8-methoxy-2-(triflouromethy)-5-quinoline]-4-oxazolecarboxamide and... von Chen, Xiaoming, Chen, Xiao, Yin, Jianguo, Fu, Xiaoyong, Blythin, David J, Kuang, Rongze, Shue, Ho-Jane, Trzaska, Scott, Tang, Chee-Wah, Liotta, Vincenzo, Shabani, Zaher

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Synthesis and NK 1 /NK 2 Binding Activities of a Series of Diacyl‐Substituted 2‐Arylpiperazines von Blythin, David J., Chen, Xiao, Piwinski, John J., Shih, Neng‐Yang, Shue, Ho‐Jane, Anthes, John C., McPhail, Andrew T.

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SELECTIVE NEUROKININ ANTAGONISTS von Shue, Ho-Jane, Shih, Neng-Yang, Reichard, Gregory, Paliwal, Sunil, Blythin, David, Piwinski, John, Xiao, Dong, Chen, Xiao

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