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Construction of sequence-selective peptide receptors from conformationally restricted eta- and theta- amino acids.
Ryan, K; Still, W C.
Affiliation
  • Ryan K; Department of Chemistry, Columbia University, New York, NY 10027, USA.
Bioorg Med Chem Lett ; 9(18): 2673-8, 1999 Sep 20.
Article in En | MEDLINE | ID: mdl-10509914
ABSTRACT
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.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Receptors, Peptide / Amino Acids Language: En Journal: Bioorg Med Chem Lett Journal subject: BIOQUIMICA / QUIMICA Year: 1999 Document type: Article Affiliation country: Estados Unidos
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Receptors, Peptide / Amino Acids Language: En Journal: Bioorg Med Chem Lett Journal subject: BIOQUIMICA / QUIMICA Year: 1999 Document type: Article Affiliation country: Estados Unidos