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pubmed-article:16953513pubmed:dateCreated2006-11-22lld:pubmed
pubmed-article:16953513pubmed:abstractTextPochonins A-F were recently characterized as six new members of the naturally occurring family of 14-membered resorcylic acid lactones. As there are a high number of ATPase and kinase inhibitors among natural resorcylic lactones, a library based on the pochonin scaffold, with five points of diversity, was prepared which includes diversity beyond that of the natural analogues. The library was synthesized by using solid-supported reagents amenable to automation. Testing the library for its inhibition against a panel of 24 kinases at 10 microM afforded a >14 % hit rate. These results demonstrate the potential of the resorcylides towards the inhibition of therapeutically relevant kinases.lld:pubmed
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pubmed-article:16953513pubmed:pagination8819-34lld:pubmed
pubmed-article:16953513pubmed:dateRevised2009-8-4lld:pubmed
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pubmed-article:16953513pubmed:year2006lld:pubmed
pubmed-article:16953513pubmed:articleTitleDiversity-oriented synthesis of pochonins and biological evaluation against a panel of kinases.lld:pubmed
pubmed-article:16953513pubmed:affiliationOrganic and Bioorganic Chemistry Laboratory, Institut de Science et Ingénierie Supramoléculaires, Université Louis Pasteur-CNRS, 8 allée Gaspard Monge, 67000 Strasbourg, France.lld:pubmed
pubmed-article:16953513pubmed:publicationTypeJournal Articlelld:pubmed
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pubmed-article:16953513pubmed:publicationTypeEvaluation Studieslld:pubmed