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Pharmaceutical Research|June 25, 2025
First-in-Class Clinically Investigated Oral Factor D Inhibitors for the Treatment of Complement-Mediated DiseasesVenkat R Gadhachanda, Jason A Wiles, Steven D Podos, et al.Bioorganic & Medicinal Chemistry Letters|October 7, 2018
Ferrocene-based inhibitors of hepatitis C virus replication that target NS5A with low picomolar in vitro antiviral activityVenkat R Gadhachanda, Kyle J Eastman, Qiuping Wang, et al.Journal of Medicinal Chemistry|March 24, 2011
Exploration of the activity of 7-pyrrolidino-8-methoxyisothiazoloquinolones against methicillin-resistant Staphylococcus aureus (MRSA)Ha Young Kim, Jason A Wiles, Qiuping Wang, et al.Bioorganic & Medicinal Chemistry Letters|March 14, 2007
Small molecule inhibitors of E. coli primase, a novel bacterial targetAtul Agarwal, Shirley Louise-May, Jane A Thanassi, et al.Bioorganic & Medicinal Chemistry Letters|December 13, 2005
Biological evaluation of isothiazoloquinolones containing aromatic heterocycles at the 7-position: In vitro activity of a series of potent antibacterial agents that are effective against methicillin-resistant Staphylococcus aureusJason A Wiles, Yongsheng Song, Qiuping Wang, et al.Bioorganic & Medicinal Chemistry Letters|December 13, 2005
Isothiazoloquinolones containing functionalized aromatic hydrocarbons at the 7-position: synthesis and in vitro activity of a series of potent antibacterial agents with diminished cytotoxicity in human cellsJason A Wiles, Qiuping Wang, Edlaine Lucien, et al.Journal of Medicinal Chemistry|January 19, 2007
Isothiazoloquinolones with enhanced antistaphylococcal activities against multidrug-resistant strains: effects of structural modifications at the 6-, 7-, and 8-positionsQiuping Wang, Edlaine Lucien, Akihiro Hashimoto, et al.Pageof 2