Elizabeth Tinney

Biaryl ethers as novel non-nucleoside reverse transcriptase inhibitors with improved potency against key mutant viruses.

Kenneth D Anderson, M. Lai, J. Vacca, 2009, Journal of medicinal chemistry.

Biaryl ethers as potent allosteric inhibitors of reverse transcriptase and its key mutant viruses: aryl substituted pyrazole as a surrogate for the pyrazolopyridine motif.

Kenneth D Anderson, M. Lai, J. Vacca, 2010, Bioorganic & medicinal chemistry letters.

Discovery of platencin, a dual FabF and FabH inhibitor with in vivo antibiotic properties

Jun Wang, Olga Genilloud, Oscar Salazar, 2007, Proceedings of the National Academy of Sciences.

2-Aminobenzophenones as a novel class of bradykinin B1 receptor antagonists.

M. Bock, R. Freidinger, R. Chang, 2008, Journal of medicinal chemistry.

Substituted tetrahydroquinolines as potent allosteric inhibitors of reverse transcriptase and its key mutants.

Kenneth D Anderson, Youwei Yan, M. Lai, 2009, Bioorganic & Medicinal Chemistry Letters.