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Bioorganic & Medicinal Chemistry Letters|February 7, 2006
The SAR of 4-substituted (6,6-bicyclic) piperidine cathepsin S inhibitorsCheryl A Grice, Kevin Tays, Haripada Khatuya, et al.Scientific Reports|May 27, 2021
Preclinical and clinical characterization of the RORγt inhibitor JNJ-61803534Xiaohua Xue, Aimee De Leon-Tabaldo, Rosa Luna-Roman, et al.The Journal of Rheumatology|July 17, 2016
Toreforant, A Histamine H4 Receptor Antagonist, in Patients with Active Rheumatoid Arthritis Despite Methotrexate Therapy: Results of 2 Phase II StudiesRobin L Thurmond, Andrew Greenspan, Waldemar Radziszewski, et al.The Journal of Pharmacology and Experimental Therapeutics|January 15, 2004
A potent and selective histamine H4 receptor antagonist with anti-inflammatory propertiesRobin L Thurmond, Pragnya J Desai, Paul J Dunford, et al.Bioorganic & Medicinal Chemistry Letters|June 15, 2010
Diazinones as P2 replacements for pyrazole-based cathepsin S inhibitorsMichael K Ameriks, Scott D Bembenek, Matthew T Burdett, et al.European Journal of Pharmacology|May 22, 2020
Selective inhibition of peripheral cathepsin S reverses tactile allodynia following peripheral nerve injury in mouseWilliam A Eckert, John J M Wiener, Hui Cai, et al.Bioorganic & Medicinal Chemistry Letters|February 16, 2010
Discovery and SAR of novel pyrazole-based thioethers as cathepsin S inhibitors: part 1Alice Lee-Dutra, Danielle K Wiener, Kristen L Arienti, et al.Journal of Medicinal Chemistry|September 5, 2003
The first potent and selective non-imidazole human histamine H4 receptor antagonistsJill A Jablonowski, Cheryl A Grice, Wenying Chai, et al.Journal of Medicinal Chemistry|December 22, 2005
Preparation and biological evaluation of indole, benzimidazole, and thienopyrrole piperazine carboxamides: potent human histamine h(4) antagonistsJennifer D Venable, Hui Cai, Wenying Chai, et al.Pageof 8