Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1366391 | Bioorganic & Medicinal Chemistry Letters | 2007 | 4 Pages |
Abstract
Diaryl imidazo[1,2-a]pyridine derivatives, such as 6a and 7i, have been synthesized and found to be potent inhibitors of parasite PKG activity. The most potent compounds are the 7-isopropylaminomethyl analog 6a and 2-isopropylamino analog 7i. These compounds are also fully active in in vivo assay as anticoccidial agents at 25 ppm in feed.
Graphical abstractDiaryl imidazo[1,2-a]pyridine derivatives bearing N-alkyl amino substituents have been synthesized and evaluated as highly potent Et-PKG inhibitor and efficacious anticoccidial agents.Figure optionsDownload full-size imageDownload as PowerPoint slide
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Gui-Bai Liang, Xiaoxia Qian, Dennis Feng, Michael Fisher, Christine M. Brown, Anne Gurnett, Penny Sue Leavitt, Paul A. Liberator, Andrew S. Misura, Tamas Tamas, Dennis M. Schmatz, Matthew Wyvratt, Tesfaye Biftu,