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Józef Oleksyszyn

Director/ Research Scientist
Chemistry
Wrocław University of Technology
Poland

Biography

Józef Oleksyszyn has recived his Ph.D. (1974-1977) and D.S. (doctor of sciences, habilitation, 1978-1986) from Faculty of Chemistry, Wrocław University of Technology. Currently he is professor of biochemistry at that place. Two postdoctoral scholarship. The first (1982-1984) at Department of Chemistry, Michigen University with prof. Arthur Ashe and the second one at Georgia Institute of Technology with prof. James C. Powers. During the period of 1990-2000 has been working in few biotechnology companies including CORTECH Inc., (Denver,CO), OsteoArthritis Inc., (Boston, MA) and DYAX (Boston, MA), at positions from research scientist to the Director of Chemical Sciences. One of the compounds, inhibitor of human neutrophil elastase, designed and synthesized by him went to the clinical trial (Cortech). He discovered an amidoalkylation reaction of trivalent phosphorus derivatives, named in literature sometimes “Oleksyszyn reaction”. In prof. Powers lab he discovered a new class of selective and potent, serine protease inhibitors – diaryl 1-aminoalkylphosphonates. In 2002 he returned to Wrocław Technology University, where he build-up the Division of Medicinal Chemistry and Microbiology that he has been headed during the period 2006-2011. His research resulted in more than 70 publications in reputed journals and more than 50 patents and patents applications, including 8 USA patents. His is a member of American Chemical Society. He has been serving as editorial member of several reputed journal like Journal Anti-cancer Agents in Medicinal Chemistry, American Journal of Cancer Prevention, Journal of Pharmacological & Biomedical Analysis, Cell Biology:Research & Therapy, and expert Revivers for several Journals.

Research Interest

His research interest include a new approaches for the anticancer therapies, enzyme inhibitors as a new drugs, including new antibacterial drugs, inhibitors of proteolytic enzymes as a new drug generation.

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