Cyclic urea derivatives as potent NK1 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 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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Novel histamine H3 receptor antagonists based on the 4-[(1H-imidazol-4-yl)methyl]piperidine scaffold von VACCARO, Wayne D, SHER, Rosy, WILLIAMS, Shirley M, WU, Ren-Long, SHE, H. Susan, RIVELLI, Maria A, MUTTER, Jennifer C, CORBOZ, Michel R, HEY, John A, FAVREAU, Leonard, BERLIN, Michael, SHIH, Neng-Yang, ASLANIAN, Robert, SCHWERDT, John H, MCCORMICK, Kevin D, PIWINSKI, John J, WEST, Robert E, ANTHES, John C

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Novel histamine H 3 receptor antagonists based on the 4-[(1 H-imidazol-4-yl)methyl]piperidine scaffold von Vaccaro, Wayne D., Sher, Rosy, Berlin, Michael, Shih, Neng-Yang, Aslanian, Robert, Schwerdt, John H., McCormick, Kevin D., Piwinski, John J., West, Robert E., Anthes, John C., Williams, Shirley M., Wu, Ren-Long, She, H. Susan, Rivelli, Maria A., Mutter, Jennifer C., Corboz, Michel R., Hey, John A., Favreau, Leonard

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Cyclic urea derivatives as potent NK sub(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 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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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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Enantiomerization of an atropisomeric drug von Friary, Richard J., Spangler, Michael, Osterman, Rebecca, Schulman, Lara, Schwerdt, John H.

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Oxidative cleavage of a tricyclic pyridone to a bicyclic lactam-dione von Friary, Richard J., Schwerdt, John H.

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Intramolecular transaminations of enaminones: a synthesis of fused, polycyclic, N-aryl pyridones von Friary, Richard J., Seidl, Vera, Schwerdt, John H., Cohen, Marvin P., Hou, Donald, Nafissi, Mehdi

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Intermolecular transaminations of enaminones: a synthesis of fused, polycyclic, N-aryl pyridones von Friary, Richard J., Seidl, Vera, Schwerdt, John H., Chan, Tze-Ming, Cohen, Marvin P., Conklin, Edward R., Duelfer, Timothy, Hou, Donald, Nafissi, Mehdi, Runkle, Robert L., Tahbaz, Pirouz, Tiberi, Robert L., Mc Phail, Andrew T.

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INHIBITORS OF DIACYLGLYCEROL ACYLTRANSFERASE von LEE, JOE, F, TING, PAULINE, C, CAPLEN, MARY ANN, KUANG, RONGZE, CAO, JIANHUA, KIM, JAE-HUN, CHAN, TIN-YAU, SCHWERDT, JOHN, H, ASLANIAN, ROBERT, G, WU, HEPING, KIM, HYUNJIN, KIM, DAVID, WON-SHIK, ZORN, NICOLAS

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SUBSTITUTED 2-QUINOLYL-OXAZOLES USEFUL AS PDE4 INHIBITORS von GU, DANLIN, CHEN, XIAO, HUANG, YING, BLYTHIN, DAVID, SHIH, NENG-YANG, XIAO, LI, SCHWERDT, JOHN H, KUANG, RONGZE, WONG, SHINGUN, TING, PAULINE C, CAO, JIANHUA, SHUE, HO-JANE

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Substituted 2-quinolyl-oxazoles useful as PDE4 inhibitors von GU, DANLIN, SCHWERDT, JOHN, H, CHEN, XIAO, HUANG, YING, BLYTHIN, DAVID, SHIH, NENG-YANG, XIAO, LI, TING, PAULINE, C, KUANG, RONGZE, WONG, SHINGUN, CAO, JIANHUA, SHUE, HO-JANE

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Substituted 2-quinolyl-oxazoles useful as PDE4 inhibitors von GU, DANLIN, HUANG, YING, CHEN, XIAO, BLYTHIN, DAVID, SHIH, NENG-YANG, XIAO, LI, SCHWERDT, JOHN H, KUANG, RONGZE, WONG, SHINGUN, TING, PAULINE C, CAO, JIANHUA, SHUE, HO-JANE

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INHIBITORS OF DIACYLGLYCEROL ACYLTRANSFERASE von LEE, JOE, F, TING, PAULINE, C, CAPLEN, MARY ANN, KUANG, RONGZE, CAO, JIANHUA, KIM, JAE-HUN, CHAN, TIN-YAU, SCHWERDT, JOHN, H, ASLANIAN, ROBERT, G, WU, HEPING, KIM, HYUNJIN, KIM, DAVID, WON-SHIK, ZORN, NICOLAS

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INHIBITORS OF DIACYLGLYCEROL ACYLTRANSFERASE von SCHWERDT, JOHN, H, LEE, JOE, F, ASLANIAN, ROBERT, G, WU, HEPING, TING, PAULINE, C, CAPLEN, MARY ANN, KIM, HYUNJIN, KUANG, RONGZE, KIM, DAVID, WON-SHIK, ZHOU, GANG, ZORN, NICOLAS, CAO, JIANHUA

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Substituted 2-quinolyl-oxazoles useful as PDE4 inhibitors von GU, DANLIN, CHEN, XIAO, HUANG, YING, BLYTHIN, DAVID, SHIH, NENG-YANG, XIAO, LI, SCHWERDT, JOHN H, KUANG, RONGZE, WONG, SHINGUN, TING, PAULINE C, CAO, JIANHUA, SHUE, HO-JANE

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Substituted 2-quinolyl-oxazoles useful as PDE4 inhibitors von SHUE HO-JANE,CHEN XIAO,SHIH NENG-YANG,CAO JIANHUA,HUANG YING,KUANG RONGZE,BLYTHIN DAVID,GU DANLIN,SCHWERDT JOHN H.,TING PAULINE C.,WONG SHINGUN,XIAO LI

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