The Journal of Organic Chemistry · 2006 · 54 citations · 16 references
PharmacyBiochemistryMedicinal ChemistryCombinatorial ChemistryDrug DesignDrug DiscoveryBioinorganic ChemistryChemical Library DesignCombinatorial SynthesisConjugation ReactionsDisulfide Bond FormationLigand BindingCombinatorial Library DesignCombinatorial Library SynthesisDisulfide Bond ChemistryDisulfide Exchange ChemistryDynamic Combinatorial LibrariesHigh-resolution Mass AnalysisHigh-resolution SpectrometryThiol-disulfide Exchange
A dynamic combinatorial library of thiocolchicine-podophyllotoxin derivatives based on the disulfide bond exchange reaction is described. The influence of a biological target on the composition of the reaction mixture has been demonstrated. Use of high-resolution ESI mass spectrometry to evaluate the composition of the mixture shows promise for the design of new large libraries. The biological evaluation demonstrates that formation of a divalent compound affords a new chemical entity whose biological activity is not merely the sum of the single ligands activities, thus reflecting a different interaction with the biological target.
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