Synthesis and biological activity of oxytocin analogues containing conformationally-restricted residues in position 7

European Journal of Medicinal Chemistry

Volumn 42, Issue 6, 2007, Pages 799-806

  Fragiadaki, Maria ^a   Magafa, Vassiliki ^a   Borovicková, Lenka ^b   Slaninová, Jiřina ^b   Cordopatis, Paul ^a  

^a UNIVERSITY OF PATRAS   (Greece)

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

Author keywords

Aminoisobutyric acid; 1,2,3,4 Tetrahydroisoquinoline 3 carboxylic acid; Biological activity; l t Butylglycine; Oxytocin analogues; Pipecolic acid

Indexed keywords

OXYTOCIN DERIVATIVE;

ANIMAL TISSUE; ARTICLE; BINDING AFFINITY; CONFORMATION; DRUG MECHANISM; DRUG POTENCY; IN VITRO STUDY; NONHUMAN; RAT; RECEPTOR BINDING; SUBSTITUTION REACTION; SYNTHESIS;

AMINO ACID SEQUENCE; ANIMALS; FEMALE; HUMANS; OXYTOCIN; PROTEIN CONFORMATION; RATS; RECEPTORS, OXYTOCIN; STRUCTURE-ACTIVITY RELATIONSHIP; UTERINE CONTRACTION; VASOPRESSINS;

EID: 34249669778     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2006.12.016     Document Type: Article

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