| Literature DB >> 8064796 |
R N Zuckermann1, E J Martin, D C Spellmeyer, G B Stauber, K R Shoemaker, J M Kerr, G M Figliozzi, D A Goff, M A Siani, R J Simon.
Abstract
Screening a diverse, combinatorial library of ca. 5000 synthetic dimer and trimer N-(substituted)glycine "peptides" yielded novel, high-affinity ligands for 7-transmembrane G-protein-coupled receptors. The peptoid library was efficiently assembled using readily available chemical building blocks. The choice of side chains was biased to resemble known ligands to 7-transmembrane G-protein-coupled receptors. All peptides were screened in solution-phase, competitive radioligand-binding assays. Peptoid trimer CHIR 2279 binds to the alpha 1-adrenergic receptor with a Ki of 5 nM, and trimer CHIR 4531 binds to the mu-opiate receptor with a Ki of 6 nM. This represents the first example of the discovery of high-affinity receptor ligands from a combinatorial library of non-natural chemical entities.Entities:
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Year: 1994 PMID: 8064796 DOI: 10.1021/jm00043a007
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446