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• W2139548062 abstract "Topological templates disposing orthogonally protected reactive sites in defined spatial positions of a variable degree of flexibility can serve as a pool for the selective functionalization by groups thought to interact with an acceptor molecule. This strategy is exemplified by the chemo-selective ligation of amino-acid residues to a cyclic peptide as a structural motif (template-assembled side chains; TASK) applying the concept of combinatorial libraries. Binding assays to a monoclonal antibody allow for the delineation of a lead compound mimicking the structural features of a discontinuous epitope. The conceptually novel approach may serve as a tool in molecular recognition studies and in drug development." @default.
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• W2139548062 date "1995-01-01" @default.
• W2139548062 modified "2023-09-24" @default.
• W2139548062 title "Topological templates as tool in molecular recognition and peptide mimicry: Synthesis of a TASK library" @default.
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• W2139548062 doi "https://doi.org/10.1002/jmr.300080105" @default.
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