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Mol Divers ; 1(2): 109-12, 1996 Feb.
Article in English | MEDLINE | ID: mdl-9237199

ABSTRACT

A strategy for high-throughput evaluation of combinatorial compound libraries is reported, which circumvents the necessity to test complex mixtures. The method is based on a new combination of protecting groups, solid-phase linker and tags. The bulk of the library first undergoes a binding assay with the components grafted on beads. A selection of beads carrying strong ligands is stripped from the labelled target and distributed into microvessels. The ligands are cleaved and rinsed into microeluates. Subsequently, a more detailed characterization with a functional assay in solution determines the best performers, which are identified through the peptidic tag left behind on the corresponding mother bead.


Subject(s)
Directed Molecular Evolution/methods , Peptide Library , Chemistry, Organic , Drug Design , Drug Evaluation, Preclinical , Humans , In Vitro Techniques , Ligands , Molecular Structure , Oligopeptides/chemical synthesis , Oligopeptides/chemistry , Oligopeptides/pharmacology , Organic Chemistry Phenomena , Solutions , Thrombin/antagonists & inhibitors
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