Suzanne S Stokes, Ph.D.
|1994-1999||Chemistry||University of Wisconsin, Madison, Madison, WI|
Area:Organic synthesis, medicinal chemistry
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|Murphy-Benenato K, Wang H, McGuire HM, et al. (2014) Identification through structure-based methods of a bacterial NAD(+)-dependent DNA ligase inhibitor that avoids known resistance mutations. Bioorganic & Medicinal Chemistry Letters. 24: 360-6|
|Uria-Nickelsen M, Neckermann G, Sriram S, et al. (2013) Novel topoisomerase inhibitors: microbiological characterisation and in vivo efficacy of pyrimidines. International Journal of Antimicrobial Agents. 41: 363-71|
|Stokes SS, Albert R, Buurman ET, et al. (2012) Inhibitors of the acetyltransferase domain of N-acetylglucosamine-1-phosphate-uridylyltransferase/glucosamine-1-phosphate-acetyltransferase (GlmU). Part 2: Optimization of physical properties leading to antibacterial aryl sulfonamides. Bioorganic & Medicinal Chemistry Letters. 22: 7019-23|
|Green OM, McKenzie AR, Shapiro AB, et al. (2012) Inhibitors of acetyltransferase domain of N-acetylglucosamine-1-phosphate-uridyltransferase/glucosamine-1-phosphate-acetyltransferase (GlmU). Part 1: Hit to lead evaluation of a novel arylsulfonamide series. Bioorganic & Medicinal Chemistry Letters. 22: 1510-9|
|Buurman ET, Andrews B, Gao N, et al. (2011) In vitro validation of acetyltransferase activity of GlmU as an antibacterial target in Haemophilus influenzae. The Journal of Biological Chemistry. 286: 40734-42|
|Raman P, Stokes SS, Angell YM, et al. (1998) Methods to Circumvent a Difficult Coupling in the Solid-Phase Synthesis of Cyclosporine Analogues. The Journal of Organic Chemistry. 63: 5734-5735|