866785-24-2Relevant articles and documents
Camphor sulfonamide derivatives as novel, potent and selective CXCR3 antagonists
Wang, Yonghui,Busch-Petersen, Jakob,Wang, Feng,Kiesow, Terence J.,Graybill, Todd L.,Jin, Jian,Yang, Zheng,Foley, James J.,Hunsberger, Gerald E.,Schmidt, Dulcie B.,Sarau, Henry M.,Capper-Spudich, Elizabeth A.,Wu, Zining,Fisher, Laura S.,McQueney, Michael S.,Rivero, Ralph A.,Widdowson, Katherine L.
scheme or table, p. 114 - 118 (2009/04/16)
A series of N-arylpiperazine camphor sulfonamides was discovered as novel CXCR3 antagonists. The synthesis, structure-activity relationships, and optimization of the initial hit that resulted in the identification of potent and selective CXCR3 antagonists are described.
Aryl sulfonamide and sulfonyl compounds as modulators of PPAR and methods of treating metabolic disorders
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Page/Page column 51, (2010/02/14)
Aryl sulfonamide and sulfonyl compounds as modulators of peroxisome proliferator activated receptors, pharmaceutical compositions comprising the same, and methods of treating disease using the same are disclosed.