Murine CXCR1 Is a Functional Receptor for GCP-2/CXCL6 and Interleukin-8/CXCL8 von Fan, Xuedong, Patera, Andriani C., Pong-Kennedy, Amy, Deno, Gregory, Gonsiorek, Waldemar, Manfra, Denise J., Vassileva, Galya, Zeng, Ming, Jackson, Craig, Sullivan, Lee, Sharif-Rodriguez, Wanda, Opdenakker, Ghislain, Van Damme, Jo, Hedrick, Joseph A., Lundell, Daniel, Lira, Sergio A., Hipkin, R. William

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Discovery and Characterization of Vicriviroc (SCH 417690), a CCR5 Antagonist with Potent Activity against Human Immunodeficiency Virus Type 1 von STRIZKI, Julie M, TREMBLAY, Cecile, TAGAT, Jayaram R, COX, Kathleen, PRIESTLEY, Tony, SOROTA, Steve, WEI HUANG, HIRSCH, Martin, REYES, Gregory R, BAROUDY, Bahige M, XU, Serena, WOJCIK, Lisa, WAGNER, Nicole, GONSIOREK, Waldemar, HIPKIN, R. William, CHOU, Chuan-Chu, PUGLIESE-SIVO, Catherine, YUSHI XIAO

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3,4-Diamino-2,5-thiadiazole-1-oxides as potent CXCR2/CXCR1 antagonists von Biju, Purakkattle, Taveras, Arthur, Yu, Younong, Zheng, Junying, Chao, Jianhua, Rindgen, Diane, Jakway, James, Hipkin, R. William, Fossetta, James, Fan, Xuedong, Fine, Jay, Qiu, Hongchen, Merritt, J. Robert, Baldwin, John J.

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Diaminocyclobutenediones as potent and orally bioavailable CXCR2 receptor antagonists: SAR in the phenolic amide region von Aki, Cynthia, Chao, Jianping, Ferreira, Johan A., Dwyer, Michael P., Yu, Younong, Chao, Jianhua, Merritt, Robert J., Lai, Gaifa, Wu, Minglang, Hipkin, R. William, Fan, Xuedong, Gonsiorek, Waldemar, Fosseta, James, Rindgen, Diane, Fine, Jay, Lundell, Daniel, Taveras, Arthur G., Biju, Purakkattle

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Synthesis and structure–activity relationships of heteroaryl substituted-3,4-diamino-3-cyclobut-3-ene-1,2-dione CXCR2/CXCR1 receptor antagonists von Yu, Younong, Dwyer, Michael P., Chao, Jianping, Aki, Cynthia, Chao, Jianhua, Purakkattle, Biju, Rindgen, Diane, Bond, Richard, Mayer-Ezel, Rosemary, Jakway, James, Qiu, Hongchen, Hipkin, R. William, Fossetta, James, Gonsiorek, Waldemar, Bian, Hong, Fan, Xuedong, Terminelli, Carol, Fine, Jay, Lundell, Daniel, Merritt, J. Robert, He, Zhenmin, Lai, Gaifa, Wu, Minglang, Taveras, Arthur

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Expansion of SAR studies on triaryl bis sulfone cannabinoid CB sub(2) receptor ligands von Tong, Ling, Shankar, B B, Chen, Lei, Rizvi, Razia, Kelly, Joseph, Gilbert, Eric, Huang, Chunli, Yang, De-Yi, Kozlowski, Joseph A, Shih, N-Y, Gonsiorek, W, Hipkin, RWilliam, Malikzay, Asra, Lunn, Charles A, Lundell, Daniel J

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Non-aromatic A-ring replacement in the triaryl bis-sulfone CB2 receptor inhibitors von Gilbert, Eric J., Zhou, Guowei, Wong, Michael K.C., Tong, Ling, Shankar, Bandarpalle B., Huang, Chunli, Kelly, Joseph, Lavey, Brian J., McCombie, Stuart W., Chen, Lei, Rizvi, Razia, Dong, Youhao, Shu, Youheng, Kozlowski, Joseph A., Shih, Neng-Yang, Hipkin, R. William, Gonsiorek, Waldemar, Malikzay, Asra, Lunn, Charles A., Favreau, Len, Lundell, Daniel J.

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Triaryl bis-sulfones as cannabinoid-2 receptor ligands: SAR studies von Shankar, Bandarpalle B., Lavey, Brian J., Zhou, Guowei, Spitler, James A., Tong, Ling, Rizvi, Razia, Yang, De-Yi, Wolin, Ronald, Kozlowski, Joseph A., Shih, Neng-Yang, Wu, Jie, Hipkin, R. William, Gonsiorek, Waldemar, Lunn, Charles A.

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