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Journal of Virology|March 31, 2006
Envelope conformational changes induced by human immunodeficiency virus type 1 attachment inhibitors prevent CD4 binding and downstream entry eventsHsu-Tso Ho, Li Fan, Beata Nowicka-Sans, et al.Bioorganic & Medicinal Chemistry Letters|September 5, 2020
Structure-based amelioration of PXR transactivation in a novel series of macrocyclic allosteric inhibitors of HIV-1 integrasePrasanna Sivaprakasam, Zhongyu Wang, Nicholas A Meanwell, et al.Antimicrobial Agents and Chemotherapy|May 2, 2012
In vitro antiviral characteristics of HIV-1 attachment inhibitor BMS-626529, the active component of the prodrug BMS-663068Beata Nowicka-Sans, Yi-Fei Gong, Brian McAuliffe, et al.Journal of Medicinal Chemistry|January 5, 2019
5,6,7,8-Tetrahydro-1,6-naphthyridine Derivatives as Potent HIV-1-Integrase-Allosteric-Site InhibitorsKevin M Peese, Christopher W Allard, Timothy Connolly, et al.Bioorganic & Medicinal Chemistry|May 23, 2022
Scaffold modifications to the 4-(4,4-dimethylpiperidinyl) 2,6-dimethylpyridinyl class of HIV-1 allosteric integrase inhibitorsKyle Parcella, Manoj Patel, Yong Tu, et al.ACS Medicinal Chemistry Letters|November 20, 2024
Invention of VH-937, a Potent HIV-1 Maturation Inhibitor with the Potential for Infrequent Oral Dosing in HumansSing-Yuen Sit, Yan Chen, Jie Chen, et al.ACS Medicinal Chemistry Letters|June 16, 2022
Discovery and Preclinical Profiling of GSK3839919, a Potent HIV-1 Allosteric Integrase InhibitorKyle Parcella, Tao Wang, Kyle Eastman, et al.Proceedings of the National Academy of Sciences of the United States of America|September 8, 2011
Inhibition of influenza virus replication via small molecules that induce the formation of higher-order nucleoprotein oligomersSamuel W Gerritz, Christopher Cianci, Sean Kim, et al.Pageof 2