The orthosteric agonist 2-chloro-5-hydroxyphenylglycine activates mGluR5 and mGluR1 with similar efficacy and potency

BMC Pharmacology

Volumn 12, Issue , 2012, Pages

  Kammermeier, Paul J ^a  

^a UNIVERSITY OF ROCHESTER MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

2 CHLORO 5 HYDROXYPHENYLGLYCINE; COMPLEMENTARY DNA; ION CHANNEL; METABOTROPIC RECEPTOR 1; METABOTROPIC RECEPTOR 5;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BIOASSAY; CALCIUM CURRENT; CONTROLLED STUDY; DRUG EFFICACY; DRUG POTENCY; INHIBITION KINETICS; MALE; MODULATION; NONHUMAN; POTASSIUM CURRENT; PROTEIN EXPRESSION; RAT; SIGNAL TRANSDUCTION; SUPERIOR CERVICAL GANGLION; SYMPATHETIC NERVE CELL;

ANIMALS; CALCIUM; EXCITATORY AMINO ACID AGONISTS; GLYCINE; MALE; NEURONS; PHENYLACETATES; RATS; RATS, WISTAR; RECEPTORS, METABOTROPIC GLUTAMATE; SUPERIOR CERVICAL GANGLION;

EID: 84861476471     PISSN: None     EISSN: 14712210     Source Type: Journal    
DOI: 10.1186/1471-2210-12-6     Document Type: Article

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