Optically active aromatic amino acids. Part VI. Synthesis and properties of (Leu5)-enkephalin analogues containing O-methyl-L-tyrosine1 with ring substitution at position 3'

Journal of Peptide Science

Volumn 6, Issue 6, 2000, Pages 280-289

  Arnold, Zdzisaw S ^a   Schiller, Peter W ^b  

^a Laboratory of Materials and Consumer Packaging Testing   (Poland)

^b CLIN RESEARCH INSTITUTE OF MONTREAL   (Canada)

Author keywords

Leu5 enkephalin analogues; Biological activity; Guinea pig ileum assay; Mouse vas deferens assay; Peptide synthesis; Tyrosine analogues

Indexed keywords

AROMATIC AMINO ACID; HYDROXYL GROUP; LEUCINE ENKEPHALIN DERIVATIVE; LEUCINE ENKEPHALIN[1 O METHYLTYROSINE] DERIVATIVE; MU OPIATE RECEPTOR AGONIST; NALOXONE; NALTREXONE; OPIATE; UNCLASSIFIED DRUG;

ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DRUG ACTIVITY; DRUG STRUCTURE; DRUG SYNTHESIS; GUINEA PIG; ILEUM; MOUSE; NONHUMAN; OPTICAL ROTATION; PRIORITY JOURNAL; VAS DEFERENS;

AMINO ACIDS; ANIMALS; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; ELECTRONS; GUINEA PIGS; ILEUM; INHIBITORY CONCENTRATION 50; LEUCINE; MAGNETIC RESONANCE SPECTROSCOPY; MALE; METHYLTYROSINES; MICE; MODELS, CHEMICAL; ULTRAVIOLET RAYS; VAS DEFERENS;

CAVIA PORCELLUS; SUS SCROFA;

EID: 0033828942     PISSN: 10752617     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-1387(200006)6:6<280::AID-PSC252>3.0.CO;2-0     Document Type: Article

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