Synthesis of methylated phenylalanines via hydrogenolysis of corresponding 1,2,3,4‐tetrahydroisoquinoline‐3‐carboxylic acids: Synthesis and biological activity of oxytocin analogs with methylated phenylalanines in position 2

International Journal of Peptide and Protein Research

Volumn 43, Issue 1, 1994, Pages 62-68

  MAJER, PAVEL ^a   SLANINOVÁ, JIŘINA ^a   LEBL, MICHAL ^b  

^a INSTITUTE OF ORGANIC CHEMISTRY AND BIOCHEMISTRY   (Czech Republic)

^b Selectide Corporation   (United States)

Author keywords

hydrogenolysis of 1.2.3.1 tetrahydroisoquinolines; ortho methylated phenylalanines; oxytocin analogs; uterotonic inhibitors

Indexed keywords

OXYTOCIN; OXYTOCIN DERIVATIVE; PHENYLALANINE DERIVATIVE;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; INTRAUTERINE PRESSURE; METHYLATION; PEPTIDE SYNTHESIS; RAT;

AMINO ACID SEQUENCE; ANIMAL; COMPARATIVE STUDY; FEMALE; HYDROGEN; ISOQUINOLINES; METHYLATION; MOLECULAR SEQUENCE DATA; MOLECULAR STRUCTURE; OLIGOPEPTIDES; OXYTOCIN; PHENYLALANINE; PROTEIN CONFORMATION; RATS; RATS, WISTAR; STEREOISOMERISM; STRUCTURE-ACTIVITY RELATIONSHIP; SUPPORT, NON-U.S. GOV'T; UTERUS;

EID: 0027983033     PISSN: 03678377     EISSN: 13993011     Source Type: Journal    
DOI: 10.1111/j.1399-3011.1994.tb00376.x     Document Type: Article

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