|
Volumn 14, Issue 13, 2006, Pages 4393-4401
|
Synthesis of enantiopure Δ2-isoxazoline derivatives and evaluation of their affinity and efficacy profiles at human β-adrenergic receptor subtypes
|
Author keywords
2 Isoxazoline derivatives; Antagonist; Binding affinity; Efficacy; Human adrenergic receptor subtypes; Synthesis
|
Indexed keywords
3 ISOPROPENYL DERIVATIVE;
ALKENYL GROUP;
BETA 1 ADRENERGIC RECEPTOR;
BETA 2 ADRENERGIC RECEPTOR;
BETA 3 ADRENERGIC RECEPTOR;
BETA ADRENERGIC RECEPTOR;
DELTA 2 IDOXAZOLINE DERIVATIVE;
DELTA 2 ISOXAZOLIN 5 YL ETHANOLAMINE DERIVATIVE;
ISOXAZOLINE DERIVATIVE;
UNCLASSIFIED DRUG;
BETA ADRENERGIC RECEPTOR BLOCKING AGENT;
ISOXAZOLE DERIVATIVE;
ANIMAL CELL;
ARTICLE;
BINDING AFFINITY;
CONTROLLED STUDY;
CYCLOADDITION;
DRUG EFFICACY;
DRUG RECEPTOR BINDING;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENANTIOMER;
MOLECULAR RECOGNITION;
NONHUMAN;
PROTEIN EXPRESSION;
STEREOCHEMISTRY;
SUBSTITUTION REACTION;
ANIMAL;
CHEMISTRY;
CHO CELL;
CRICETULUS;
DRUG EFFECT;
HAMSTER;
HUMAN;
STEREOISOMERISM;
SYNTHESIS;
ADRENERGIC BETA-ANTAGONISTS;
ANIMALS;
CHO CELLS;
CRICETINAE;
CRICETULUS;
HUMANS;
ISOXAZOLES;
RECEPTORS, ADRENERGIC, BETA;
STEREOISOMERISM;
|
EID: 33646548291
PISSN: 09680896
EISSN: None
Source Type: Journal
DOI: 10.1016/j.bmc.2006.02.038 Document Type: Article |
Times cited : (16)
|
References (27)
|