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Novel non-benzimidazole chk2 kinase inhibitors.
McClure, Kelly J; Huang, Liming; Arienti, Kristen L; Axe, Frank U; Brunmark, Anders; Blevitt, Jon; Breitenbucher, J Guy.
Afiliação
  • McClure KJ; Johnson and Johnson Pharmaceutical Research and Development, LLC, 3210 Merryfield Row, San Diego, CA 92121, USA. kmcclure@prdus.jnj.com
Bioorg Med Chem Lett ; 16(7): 1924-8, 2006 Apr 01.
Article em En | MEDLINE | ID: mdl-16442290
ABSTRACT
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.
Assuntos
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Base de dados: MEDLINE Assunto principal: Proteínas Serina-Treonina Quinases / Inibidores de Proteínas Quinases Idioma: En Ano de publicação: 2006 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Proteínas Serina-Treonina Quinases / Inibidores de Proteínas Quinases Idioma: En Ano de publicação: 2006 Tipo de documento: Article