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Methods in Molecular Medicine|March 8, 2011
Synthesis of protected lactam-bridged dipeptidesD S Perlow, R M FreidingerScience (New York, N.Y.)|November 7, 1980
Bioactive conformation of luteinizing hormone-releasing hormone: evidence from a conformationally constrained analogR M Freidinger, D F Veber, D S Perlow, et al.International Journal of Peptide and Protein Research|February 1, 1984
Conformational modifications of cyclic hexapeptide somatostatin analogsR M Freidinger, D S Perlow, W C Randall, et al.Current Opinion in Chemical Biology|July 27, 1999
Nonpeptidic ligands for peptide and protein receptorsR M FreidingerTrends in Pharmacological Sciences|July 1, 1989
Non-peptide ligands for peptide receptorsR M FreidingerLife Sciences|April 2, 1984
A super active cyclic hexapeptide analog of somatostatinD F Veber, R Saperstein, R F Nutt, et al.Molecular Pharmacology|January 1, 1986
Conformationally constrained tachykinin analogs which are selective ligands for the eledoisin binding siteM A Cascieri, G G Chicchi, R M Freidinger, et al.Bioorganic & Medicinal Chemistry|September 1, 1994
Conformationally constrained o-tolylpiperazine camphorsulfonamide oxytocin antagonists. Structural modifications that provide high receptor affinity and suggest a bioactive conformationP D Williams, R G Ball, B V Clineschmidt, et al.Journal of Enzyme Inhibition|January 1, 1985
Interaction of mouse submaxillary gland renin with a statine-containing, subnanomolar, competitive inhibitorM Poe, D S Perlow, J BogerBioorganic & Medicinal Chemistry Letters|January 5, 1999
Nonpeptide oxytocin antagonists: potent, orally bioavailable analogs of L-371,257 containing a 1-R-(pyridyl)ethyl ether terminusM S Kuo, M G Bock, R M Freidinger, et al.Pageof 5