| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1396174 | European Journal of Medicinal Chemistry | 2011 | 8 Pages |
A series of highly potent indole-3-glyoxylamide based antiprion agents was previously characterized, focusing on optimization of structure–activity relationship (SAR) at positions 1–3 of the indole system. New libraries interrogating the SAR at indole C-4 to C-7 now demonstrate that introducing electron-withdrawing substituents at C-6 may improve biological activity by up to an order of magnitude, and additionally confer higher metabolic stability. For the present screening libraries, both the degree of potency and trends in SAR were consistent across two cell line models of prion disease, and the large majority of compounds showed no evidence of toxic effects in zebrafish. The foregoing observations thus make the indole-3-glyoxylamides an attractive lead series for continuing development as potential therapeutic agents against prion disease.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Indole-3-glyoxylamides substituted at C-6 show markedly improved antiprion efficiency. ► Introducing substitution at positions 4, 5 or 7 was disfavored. ► Good correlation between activity in two cell line models of prion disease. ► C-6 substituted compounds had good metabolic stability and non-toxic in zebrafish.
