The first potent nonpeptidic ligands for somatostatin, luteinizing hormone-
releasing hormone, glucagon and bradykinin receptors have been reported. No
npeptidic clinical candidates have been identified or are currently under s
tudy for substance P, bradykinin, endothelin, growth hormone secretagogue,
angiotensin, vasopressin, motilin and cholecystokinin. Design, screening, c
ombinatorial chemistry and classical medicinal chemistry all played importa
nt roles in these advances.