Synthesis of an analogue of the substance P C-terminal hexapeptide with modification at the glutaminyl and methioninyl residues and increased activity in NK-2 receptor type: Structure-activity relationships
- 31 December 1992
- journal article
- Published by Elsevier in European Journal of Medicinal Chemistry
- Vol. 27 (9) , 949-954
- https://doi.org/10.1016/0223-5234(92)90027-x
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Application of carboxylic-phosphinic mixed anhydrides in the fragment peptide synthesis of protected analogues of substance PInternational Journal of Peptide and Protein Research, 2009
- Selectivity and specificity of new, non-peptide, quinuclidine antagonists of substance PBiochemical and Biophysical Research Communications, 1991
- Potent and highly selective neurokinin antagonistsJournal of Medicinal Chemistry, 1990
- Synthesis and biological activity of substance P C-terminal hexapeptide analogues: structure-activity studiesJournal of Medicinal Chemistry, 1986
- Application of diphenylphosphinic carboxylic mixed anhydrides to peptide synthesisJournal of the Chemical Society, Perkin Transactions 1, 1985
- Nomenclature and Symbolism for Amino Acids and PeptidesEuropean Journal of Biochemistry, 1984
- Structure-activity studies on the C-terminal amide of substance PJournal of Medicinal Chemistry, 1982
- Synthesis of peptides by the solid-phase method. 7. Substance P and analogsJournal of Medicinal Chemistry, 1982
- Synthesis of 6-(Nα-acetyl-lysyl)-11-norleucine-substance P-(6-11)-hexapeptide labelled with tritium on the phenylalanine residue in position 7Journal of Labelled Compounds and Radiopharmaceuticals, 1978
- Synthesis of substance P via its sulfoxide by the repetitive excess mixed anhydride (REMA) methodRecueil des Travaux Chimiques des Pays-Bas, 1978