A highly active chemotactic peptide analog incorporating the unusual residue 1-aminocyclohexanecarboxylic acid at position 2
- 1 April 1985
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 128 (1), 339-344
- https://doi.org/10.1016/0006-291x(85)91684-5
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Cyclic tetrameric clusters of chemotactic peptides as superactive activators of lysozyme release from human neutrophilsBiochemical and Biophysical Research Communications, 1984
- Structural requirements for formyl homooligopeptide chemoattractantsBiochemistry, 1984
- Conformationally constrained chemotactic peptide analogs of high biological activityFEBS Letters, 1984
- The Stereochemistry of Peptides Containing α-Aminoisobutyric AciCritical Reviews in Biochemistry, 1984
- Formyl peptide chemoattractants: a model of the receptor on rabbit neutrophilsBiochemistry, 1982
- Further studies on the structural requirements for synthetic peptide chemoattractantsBiochemistry, 1980
- Nuclear magnetic resonance conformational studies on the chemotactic tripeptide formyl-L-methionyl-L-leucyl-L-phenylalanine. A small .beta. sheetBiochemistry, 1979
- The structure-activity relations of synthetic peptides as chemotactic factors and inducers of lysosomal secretion for neutrophils.The Journal of Experimental Medicine, 1976
- 1161. Peptides. Part XVIII. Derivatives of 1-aminocyclohexanecarboxylic acidJournal of the Chemical Society, 1965