PMID

Data

Article Title

Organization

Quantitative structure-activity relationships (QSARs) of N-terminus fragments of NK1 tachykinin antagonists: a comparison of classical QSARs and three-dimensional QSARs from similarity matrices.

Cambridge University Forvie Site

Use of a dipeptide chemical library in the development of non-peptide tachykinin NK3 receptor selective antagonists.

Cambridge University Forvie Site

PD 176252--the first high affinity non-peptide gastrin-releasing peptide (BB2) receptor antagonist.

Cambridge University Forvie Site

Utilization of an intramolecular hydrogen bond to increase the CNS penetration of an NK(1) receptor antagonist.

Cambridge University Forvie Site