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Volumn 45, Issue 17, 2002, Pages 3805-3808
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Characterization of orally active nonpeptide vasopressin V2 receptor agonist. Synthesis and biological evaluation of both the (5R)- and (5S)-enantioisomers of 2-[1-(2-chloro-4-pyrrolidin-1-yl-benzoyl)- 2,3,4,5-tetrahydro-1H-1-benzazepin-5-yl]-N-isopropylacetamide
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Author keywords
[No Author keywords available]
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Indexed keywords
2 [1 (2 CHLORO 4 PYRROLIDIN 1 YLBENZOYL) 2,3,4,5 TETRAHYDRO 1H 1 BENZAZEPIN 5 YL] N ISOPROPYLACETAMIDE;
BENZAZEPINE DERIVATIVE;
CYCLIC AMP;
HORMONE RECEPTOR STIMULATING AGENT;
UNCLASSIFIED DRUG;
VASOPRESSIN V2 RECEPTOR;
ANIMAL EXPERIMENT;
ANTIDIURESIS;
ARTICLE;
BINDING AFFINITY;
COMPARATIVE STUDY;
CONTROLLED STUDY;
DOSE RESPONSE;
DRUG POTENCY;
DRUG SYNTHESIS;
ENANTIOMER;
FEMALE;
HUMAN;
HUMAN CELL;
IN VIVO STUDY;
ISOMER;
NONHUMAN;
RAT;
RAT STRAIN;
X RAY CRYSTALLOGRAPHY;
ADMINISTRATION, ORAL;
ANIMALS;
CRYSTALLOGRAPHY, X-RAY;
CYCLIC AMP;
HELA CELLS;
HUMANS;
RADIOLIGAND ASSAY;
RATS;
RATS, BRATTLEBORO;
RECEPTORS, VASOPRESSIN;
STEREOISOMERISM;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 0037103346
PISSN: 00222623
EISSN: None
Source Type: Journal
DOI: 10.1021/jm020133q Document Type: Article |
Times cited : (50)
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References (21)
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