Synthesis and opioid activities of stereoisomers and other D-amino acid analogs of methionine-enkephalin
- 6 December 1976
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 73 (3) , 632-638
- https://doi.org/10.1016/0006-291x(76)90857-3
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- Conformation of Met5-enkephalin determined by high field PMR spectroscopyNature, 1976
- Preferential conformation of the endogenous opiate-like pentapeptide met-enkephalin in DMSO-d6 solution determined by high field 1H NMRBiochemical and Biophysical Research Communications, 1976
- Conformational energy analysis of the molecule, luteinizing hormone-releasing hormone. 2. Tetrapeptide and decapeptide analoguesJournal of the American Chemical Society, 1976
- Conformational energy analysis of the molecule, luteinizing hormone-releasing hormone. 1. Native decapeptideJournal of the American Chemical Society, 1976
- Biosynthetic origin and receptor conformation of methionine enkephalinNature, 1976
- Analogs of luteinizing hormone-releasing hormone with increased biological activity produced by D-amino acid substitutions in position 6Journal of Medicinal Chemistry, 1976
- Identification of two related pentapeptides from the brain with potent opiate agonist activityNature, 1975
- D-Trp8-somatostatin: An analog of somatostatin more potent than the native moleculeBiochemical and Biophysical Research Communications, 1975
- Synthesis and biological properties of [Leu-6]-LH-RH and [D-leu-6,desGly-NH210]-LH-RH ethylamideBiochemical and Biophysical Research Communications, 1974
- Synthetic analogs of the hypothalamic luteinizing hormone releasing factor with increased agonist or antatonist propertiesBiochemistry, 1973