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Parallel synthesis of an oligomeric imidazole-4,5-dicarboxamide library.

ABSTRACT: A library of oligomeric compounds was synthesized based on the imidazole-4,5-dicarboxylic acid scaffold along with amino acid esters and chiral diamines derived from amino acids. The final compounds incorporate nonpolar amino acids (Leu, Phe, Trp), polar amino acids (Ser, Asp, Arg), and neutral amino acids (Gly, Ala), and were designed to be useful in screening for inhibitors of protein-protein interactions. Many of the protected and deprotected oligomers show evidence of conformational isomers persistent at room temperature in aqueous solution. A total of 317 final oligomers, out of 441 targeted compounds, were obtained in high analytical purity and of sufficient quantity to submit them for high-throughput screening as part of the NIH Roadmap.

SUBMITTER: Xu Z

PROVIDER: S-EPMC2846700 | biostudies-literature | 2010 Mar

REPOSITORIES: biostudies-literature

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Parallel synthesis of an oligomeric imidazole-4,5-dicarboxamide library.

Xu Zhigang Z DiCesare John C JC Baures Paul W PW

Journal of combinatorial chemistry 20100301 2

A library of oligomeric compounds was synthesized based on the imidazole-4,5-dicarboxylic acid scaffold along with amino acid esters and chiral diamines derived from amino acids. The final compounds incorporate nonpolar amino acids (Leu, Phe, Trp), polar amino acids (Ser, Asp, Arg), and neutral amino acids (Gly, Ala), and were designed to be useful in screening for inhibitors of protein-protein interactions. Many of the protected and deprotected oligomers show evidence of conformational isomers ...[more]

PMID: 20170086

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