| Literature DB >> 24900250 |
Marc Liniger1, Christian Neuhaus1, Tatjana Hofmann1, Luca Fransioli-Ignazio1, Michel Jordi1, Peter Drueckes2, Jörg Trappe2, Doriano Fabbro2, Karl-Heinz Altmann1.
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.Entities:
Keywords: Cancer; SAR; irreversible inhibitor; kinase inhibitor; natural product; resorcylic lactone (RL); stereoselective synthesis
Year: 2010 PMID: 24900250 PMCID: PMC4018056 DOI: 10.1021/ml1001807
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345