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Kinase inhibition by deoxy analogues of the resorcylic lactone L-783277.
Liniger, Marc; Neuhaus, Christian; Hofmann, Tatjana; Fransioli-Ignazio, Luca; Jordi, Michel; Drueckes, Peter; Trappe, Jörg; Fabbro, Doriano; Altmann, Karl-Heinz.
Afiliação
  • Liniger M; Swiss Federal Institute of Technology (ETH) Zurich, Department of Chemistry and Applied Biosciences, Institute of Pharmaceutical Sciences, 8093 Zurich, Switzerland.
  • Neuhaus C; Swiss Federal Institute of Technology (ETH) Zurich, Department of Chemistry and Applied Biosciences, Institute of Pharmaceutical Sciences, 8093 Zurich, Switzerland.
  • Hofmann T; Swiss Federal Institute of Technology (ETH) Zurich, Department of Chemistry and Applied Biosciences, Institute of Pharmaceutical Sciences, 8093 Zurich, Switzerland.
  • Fransioli-Ignazio L; Swiss Federal Institute of Technology (ETH) Zurich, Department of Chemistry and Applied Biosciences, Institute of Pharmaceutical Sciences, 8093 Zurich, Switzerland.
  • Jordi M; Swiss Federal Institute of Technology (ETH) Zurich, Department of Chemistry and Applied Biosciences, Institute of Pharmaceutical Sciences, 8093 Zurich, Switzerland.
  • Drueckes P; Novartis Institute for Biomedical Research, Center for Proteomic Chemistry, Expertise Platform Kinases, 4002 Basel, Switzerland.
  • Trappe J; Novartis Institute for Biomedical Research, Center for Proteomic Chemistry, Expertise Platform Kinases, 4002 Basel, Switzerland.
  • Fabbro D; Novartis Institute for Biomedical Research, Center for Proteomic Chemistry, Expertise Platform Kinases, 4002 Basel, Switzerland.
  • Altmann KH; Swiss Federal Institute of Technology (ETH) Zurich, Department of Chemistry and Applied Biosciences, Institute of Pharmaceutical Sciences, 8093 Zurich, Switzerland.
ACS Med Chem Lett ; 2(1): 22-7, 2011 Jan 13.
Article em En | MEDLINE | ID: mdl-24900250
ABSTRACT
The natural product L-783277 is a resorcylic lactone type covalent kinase inhibitor. We have prepared the 5'-deoxy analogue of L-783277 (1) in a stereoselective fashion. Remarkably, this analogue retains almost the full kinase inhibitory potential of natural L-783277, with low nanomolar IC50 values against the most sensitive kinases, and it exhibits essentially the same selectivity profile (within the panel of 39 kinases investigated). In contrast, removal of both the 4'- and the 5'-hydroxyl groups leads to a more significant reduction in kinase inhibitory activity and so does a change in the geometry of the C7'-C8' double bond in 1 from Z to E. These findings offer new perspectives for the design of second generation resorcylic lactone-based kinase inhibitors.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2011 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2011 Tipo de documento: Article