The design of a dipeptide library for screening at peptide receptor sites

The design of a dipeptide library for screening at peptide receptor sites Design of nonpeptidal ligands for a peptide receptor: cholecystokinin antagonists The chemical synthesis of large random peptide libraries and their use for the discovery of ligands for macromolecular acceptors Discovery of Nanomolar Ligands for 7-Transmembrane G-Protein-Coupled Receptors from a Diverse N-(Substituted)glycine Peptoid Library Structure−Activity Relationships of Bifunctional Peptides Based on Overlapping Pharmacophores at Opioid and Cholecystokinin Receptors Design and Synthesis of Novel Hydrazide-Linked Bifunctional Peptides as δ/μ Opioid Receptor Agonists and CCK-1/CCK-2 Receptor Antagonists Inhibitors of Tripeptidyl Peptidase II. 2. Generation of the First Novel Lead Inhibitor of Cholecystokinin-8-Inactivating Peptidase:  A Strategy for the Design of Peptidase Inhibitors From Hit to Lead. Combining Two Complementary Methods for Focused Library Design. Application to μ Opiate Ligands Synthesis and binding affinities of analogs of cholecystokinin-(30-33) as probes for central nervous system cholecystokinin receptors Methods for drug discovery: development of potent, selective, orally effective cholecystokinin antagonists