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ACS Medicinal Chemistry Letters|February 14, 2012
Discovery of a Potent HIV Integrase Inhibitor that Leads to a Prodrug with Significant anti-HIV ActivityByung I Seo, Vinod R Uchil, Maurice Okello, et al.Antiviral Research|April 23, 2013
A novel anti-HIV active integrase inhibitor with a favorable in vitro cytochrome P450 and uridine 5'-diphospho-glucuronosyltransferase metabolism profileMaurice O Okello, Sanjay Mishra, Malik Nishonov, et al.Acta Crystallographica. Section C, Crystal Structure Communications|August 6, 2005
A non-natural dinucleotide containing an isomeric L-related deoxynucleoside: dinucleotide inhibitors of anti-HIV integrase activityM Gary Newton, Charles F Campana, Guo Chen Chi, et al.Bioorganic & Medicinal Chemistry|November 3, 2004
Synthesis and biological evaluation of 5R- and 5S-methyl substituted D- and L-configuration 1,3-dioxolane nucleoside analogsSanjib Bera, Leila Malik, Balkrishen Bhat, et al.Journal of Medicinal Chemistry|April 16, 2004
Structure-activity relationship of purine ribonucleosides for inhibition of hepatitis C virus RNA-dependent RNA polymeraseAnne B Eldrup, Charles R Allerson, C Frank Bennett, et al.Journal of Medicinal Chemistry|October 1, 2004
Structure-activity relationship of heterobase-modified 2'-C-methyl ribonucleosides as inhibitors of hepatitis C virus RNA replicationAnne B Eldrup, Marija Prhavc, Jennifer Brooks, et al.Pageof 5