Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10590939 | Bioorganic & Medicinal Chemistry Letters | 2014 | 6 Pages |
Abstract
A medicinal chemistry exploration of the human phosphodiesterase 4 (hPDE4) inhibitor cilomilast (1) was undertaken in order to identify inhibitors of phosphodiesterase B1 of Trypanosoma brucei (TbrPDEB1). T. brucei is the parasite which causes African sleeping sickness, a neglected tropical disease that affects thousands each year, and TbrPDEB1 has been shown to be an essential target of therapeutic relevance. Noting that 1 is a weak inhibitor of TbrPDEB1, we report the design and synthesis of analogs of this compound, culminating in 12b, a sub-micromolar inhibitor of TbrPDEB1 that shows modest inhibition of T. brucei proliferation.
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Authors
Emanuele Amata, Nicholas D. Bland, Charles T. Hoyt, Luca Settimo, Robert K. Campbell, Michael P. Pollastri,