Rose Bengal analogs and vesicular glutamate transporters (VGLUTs)

Bioorganic and Medicinal Chemistry

Volumn 18, Issue 18, 2010, Pages 6922-6933

  Pietrancosta, Nicolas ^a   Kessler, Albane ^a,f   Favre Besse, Franck Cyril ^a   Triballeau, Nicolas ^a,g   Quentin, Thomas ^b,c,d   Giros, Bruno ^b,c,d,e   Mestikawy, Salah El ^b,c,d,e   Acher, Francine C ^a  

^a UNIVERSITÉ PARIS DESCARTES   (France)

^b CNRS   (France)

^c INSERM   (France)

^d SORBONNE UNIVERSITÉ   (France)

^e MCGILL UNIVERSITY   (Canada)

^f GSK   (Spain)

^g NONE   (France)

Author keywords

Active binding form; Fluorescein; Glutamate; Non competitive inhibitors; Pharmacophore model; Tautomers; VACHT; VGLUT; VMAT

Indexed keywords

ACETYLCHOLINE; CARBOXYLIC ACID; FLUORESCEIN; GLUTAMIC ACID; NEUROTRANSMITTER; ROSE BENGAL; VESICULAR ACETYLCHOLINE TRANSPORTER; VESICULAR GLUTAMATE TRANSPORTER; VESICULAR MONOAMINE TRANSPORTER;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CONCENTRATION RESPONSE; CONTROLLED STUDY; DRUG POTENCY; DRUG STRUCTURE; DRUG SYNTHESIS; MOUSE; NEUROTRANSMISSION; NONHUMAN; PHARMACOPHORE; RAT; SYNAPSE VESICLE;

ANIMALS; MODELS, CHEMICAL; MODELS, MOLECULAR; RATS; RATS, SPRAGUE-DAWLEY; ROSE BENGAL; STRUCTURE-ACTIVITY RELATIONSHIP; SYNAPTIC VESICLES; VESICULAR GLUTAMATE TRANSPORT PROTEINS;

EID: 77956338566     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2010.06.069     Document Type: Article

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