Katharine Winans

Katharine Winans

SENIOR LECTURER
Phone: (603) 862-2529
Office: Chemistry, Parsons Hall Rm S151C, Durham, NH 03824
Websites:

Courses Taught

  • CHEM 403: General Chemistry I Lab
  • CHEM 403/413: General Chemistry I
  • CHEM 403/414: General Chemistry Lab
  • CHEM 404/404H: General Chemistry II
  • CHEM 404/404H/415: General Chemistry II
  • CHEM 409: Chemistry and Society
  • CHEM 411: Intro Chem Life Sciences
  • CHEM 545: Organic Chemistry

Education

  • Ph.D., Chemistry, University of California - Berkeley
  • M.A., Creative Writing, University of Houston
  • B.A., Biology/Biological Sciences, Williams College

Selected Publications

  • Hang, H. C., Yu, C., Ten Hagen, K. G., Tian, E., Winans, K. A., Tabak, L. A., & Bertozzi, C. R. (2004). Small molecule inhibitors of mucin-type O-linked glycosylation from a uridine-based library. CHEMISTRY & BIOLOGY, 11(3), 337-345. doi:10.1016/j.chembiol.2004.02.023

  • Scherman, M. S., Winans, K. A., Stern, R. J., Jones, V., Bertozzi, C. R., & McNeil, M. R. (2003). Drug targeting Mycobacterium tuberculosis cell wall synthesis: Development of a microtiter plate-based screen for UDP-galactopyranose mutase and identification of an inhibitor from a uridine-based library. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 47(1), 378-382. doi:10.1128/AAC.47.1.378-382.2003

  • Yu, C., Hang, H. C., Winans, K. A., Ten Hagen, K. G., Tabak, L. A., & Bertozzi, C. R. (2002). Identification of polypeptidyl-N-acetyl-galactosaminyltransferase (ppGalNAcT) inhibitors from a uridine-based library. In GLYCOBIOLOGY Vol. 12 (pp. 664). Retrieved from https://www.webofscience.com/

  • Winans, K. A., & Bertozzi, C. R. (2002). An inhibitor of the human UDP-GlcNAc 4-epimerase identified from a uridine-based library: A strategy to inhibit O-linked glycosylation. CHEMISTRY & BIOLOGY, 9(1), 113-129. doi:10.1016/S1074-5521(02)00093-5

  • Armstrong, J. I., Ge, X., Verdugo, D. E., Winans, K. A., Leary, J. A., & Bertozzi, C. R. (2001). A library approach to the generation of bisubstrate analogue sulfotransferase inhibitors. ORGANIC LETTERS, 3(17), 2657-2660. doi:10.1021/ol0162217

  • Shin, Y., Winans, K. A., Backes, B. J., Kent, S. B. H., Ellman, J. A., & Bertozzi, C. R. (1999). Fmoc-based synthesis of peptide-(alpha)thioesters: Application to the total chemical synthesis of a glycoprotein by native chemical ligation. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 121(50), 11684-11689. doi:10.1021/ja992881j

  • Winans, K. A., King, D. S., Rao, V. R., & Bertozzi, C. R. (1999). A chemically synthesized version of the insect antibacterial glycopeptide, diptericin, disrupts bacterial membrane integrity. BIOCHEMISTRY, 38(36), 11700-11710. doi:10.1021/bi991247f

  • Winans, K. A., & Bertozzi, C. R. (1998). Inner space exploration: the chemical biologist's guide to the cell. CHEMISTRY & BIOLOGY, 5(12), R313-R315. doi:10.1016/S1074-5521(98)90658-5

  • Rodriguez, E. C., Winans, K. A., King, D. S., & Bertozzi, C. R. (1997). A strategy for the chemoselective synthesis of O-linked glycopeptides with native sugar-peptide linkages. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 119(41), 9905-9906. doi:10.1021/ja971633p

  • WINANS, K. A., & HASHIMOTO, C. (1995). VENTRALIZATION OF THE DROSOPHILA EMBRYO BY DELETION OF EXTRACELLULAR LEUCINE-RICH REPEATS IN THE TOLL PROTEIN. MOLECULAR BIOLOGY OF THE CELL, 6(5), 587-596. doi:10.1091/mbc.6.5.587

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  • Most Cited Publications