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Bioorganic & Medicinal Chemistry Letters|April 23, 2013
Conformation constraint of anilides enabling the discovery of tricyclic lactams as potent MK2 non-ATP competitive inhibitorsDong Xiao, Anandan Palani, Xianhai Huang, et al.Bioorganic & Medicinal Chemistry Letters|September 18, 2010
Discovery of a series of potent, orally active α,α-disubstituted piperidine NK(1) antagonistsDong Xiao, Cheng Wang, Anandan Palani, et al.Bioorganic & Medicinal Chemistry Letters|December 28, 2010
Discovery of a series of potent arylthiadiazole H(3) antagonistsDong Xiao, Anandan Palani, Michael Sofolarides, et al.Journal of Medicinal Chemistry|April 2, 2005
Discovery of bicycloalkyl urea melanin concentrating hormone receptor antagonists: orally efficacious antiobesity therapeuticsMark D McBriar, Henry Guzik, Ruo Xu, et al.Journal of Medicinal Chemistry|August 14, 2020
Generation of Leads for γ-Secretase ModulationMihirbaran Mandal, Alexei Buevich, John P Caldwell, et al.Bioorganic & Medicinal Chemistry Letters|January 4, 2011
Discovery of fused 5,6-bicyclic heterocycles as γ-secretase modulatorsJun Qin, Pawan Dhondi, Xianhai Huang, et al.Journal of Medicinal Chemistry|July 22, 2005
Biaryl ureas as potent and orally efficacious melanin concentrating hormone receptor 1 antagonists for the treatment of obesityAnandan Palani, Sherry Shapiro, Mark D McBriar, et al.Bioorganic & Medicinal Chemistry Letters|February 5, 2003
Piperazine-based CCR5 antagonists as HIV-1 inhibitors. III: synthesis, antiviral and pharmacokinetic profiles of symmetrical heteroaryl carboxamidesStuart W McCombie, Jayaram R Tagat, Susan F Vice, et al.The Journal of Organic Chemistry|February 16, 2002
Synthesis of mono- and difluoronaphthoic acidsJayaram R Tagat, Stuart W McCombie, Dennis V Nazareno, et al.Virology|February 24, 2006
Interaction of small molecule inhibitors of HIV-1 entry with CCR5Christoph Seibert, Weiwen Ying, Svetlana Gavrilov, et al.Pageof 7