Chemical synthesis of human β‐endorphin(1–27) analogs by peptide segment coupling
- 1 July 1991
- journal article
- Published by Wiley in International Journal of Peptide and Protein Research
- Vol. 38 (1), 70-78
- https://doi.org/10.1111/j.1399-3011.1991.tb01412.x
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Studies on opioid receptor selectivity of β-endorphin antagonistsInternational Journal of Peptide and Protein Research, 2009
- β‐Endorphin: peripheral opioid activity of homologues from six speciesInternational Journal of Peptide and Protein Research, 1987
- Chemical synthesis of α‐inhibin‐92 by the thiocarboxyl segment coupling methodInternational Journal of Peptide and Protein Research, 1986
- Synthesis of human pancreatic growth hormone‐releasing factor and two omission analogs by segment‐coupling method in aqueous solutionInternational Journal of Peptide and Protein Research, 1984
- β‐ENDORPHIN: SYNTHESIS AND RADIORECEPTOR BINDING ACTIVITY OF βh‐ENDORPHIN‐(1–27) AND ITS ANALOGSInternational Journal of Peptide and Protein Research, 1981
- The synthesis and opiate activity of β-endorphinBiochemical and Biophysical Research Communications, 1976
- An improved polystyrene support for solid phase peptide synthesisThe Journal of Organic Chemistry, 1976
- THE METHYLSULFONYLETHYLOXYCARBONYL GROUP, A NEW AND VERSATILE AMINO PROTECTIVE FUNCTIONInternational Journal of Peptide and Protein Research, 1975
- The monitoring of reactions in solid-phase peptide synthesis with picric acidAnalytica Chimica Acta, 1972
- Solid Phase Peptide Synthesis. I. The Synthesis of a TetrapeptideJournal of the American Chemical Society, 1963