Construction of sequence-selective peptide receptors from conformationally restricted eta- and theta-amino acids

DOI: 10.1016/S0960-894X(99)00463-1

Source and publish data:

Bioorganic and Medicinal Chemistry Letters p. 2673 - 2678 (1999)

Update date:2022-08-03

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Authors:

Ryan, Kevin

Still, W. Clark

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Article abstract of DOI:10.1016/S0960-894X(99)00463-1

Oligomeric chemoreceptors for tripeptides have been constructed from a set of novel eta- and theta-amino acids. Screening against an encoded combinatorial tripeptide library has revealed two new small molecule chemoreceptor motifs with highly sequence-selective binding properties.

Full text of DOI:10.1016/S0960-894X(99)00463-1

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