Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1375193 | Bioorganic & Medicinal Chemistry Letters | 2006 | 5 Pages |
In a recent paper, [Arienti, K. L.; Brunmark, A.; Axe, F. U.; McClure, K. M.; Lee, A.; Blevitt, J.; Neff, D. K.; Huang, L.; Crawford, S.; Chennagiri, R. P.; Karlsson, L.; Brietenbucher, J. G. J. Med. Chem.2005, 48, 1873], we described the discovery of a class of benzimidazole chk2 kinase inhibitors, exemplified by compound 1, which had radio-protective effects in human T-cells subjected to ionizing radiation. Here, a series of non-benzimidazole analogs intended to define the scope of the SAR about this new series of inhibitor, and allow for refinement of the binding model of these compounds to the chk2 kinase is described.
Graphical abstractA number of benzimidazole replacements were synthesized and examined to gain a greater understanding of the SAR around this novel series of chk2 kinase inhibitors.Figure optionsDownload full-size imageDownload as PowerPoint slide