Search Results - "Baron, Bruce M"
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CoMFA, Synthesis, and Pharmacological Evaluation of (E)-3-(2-Carboxy-2-arylvinyl)-4,6-dichloro-1H-indole-2-carboxylic Acids: 3-[2-(3-Aminophenyl)-2-carboxyvinyl]-4,6-dichloro-1H-indole-2-carboxylic Acid, a Potent Selective Glycine-Site NMDA Receptor Antagonist
Published in Journal of medicinal chemistry (24-02-2005)“…(E)-3-(2-Carboxy-2-phenylvinyl)-4,6-dichloro-1H-indole-2-carboxylic acid, 1, is a potent and selective antagonist of the glycine site of the…”
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A novel adenylyl cyclase-activating serotonin receptor (5-HT7) implicated in the regulation of mammalian circadian rhythms
Published in Neuron (Cambridge, Mass.) (01-09-1993)“…We report the cloning and characterization of a novel serotonin receptor, designated as 5-HT7, which is coupled to the stimulation of adenylyl cyclase. 5-HT7…”
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Binding of 5H-Dibenzo[b,e][1,4]diazepine and Chiral 5H-Dibenzo[a,d]cycloheptene Analogs of Clozapine to Dopamine and Serotonin Receptors
Published in Journal of medicinal chemistry (01-08-1994)“…5H-Dibenzo[b,e][1,4]diazepine, dibenz[b,f]oxepin, and 5H-dibenzo[a,d]cycloheptene analogues of clozapine [8-chloro-11-(4-methylpiperazino)-5H-…”
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Two Members of a Distinct Subfamily of 5-Hydroxytryptamine Receptors Differentially Expressed in Rat Brain
Published in Proceedings of the National Academy of Sciences - PNAS (15-04-1993)“…We report two serotonin (5-hydroxytryptamine, 5-HT) receptors, MR22 and REC17, that belong to the G-protein-associated receptor superfamily. MR22 and REC17 are…”
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Pharmacological characterization of MDL 105,519, an NMDA receptor glycine site antagonist
Published in European journal of pharmacology (04-04-1997)“…MDL 105,519, ( E)-3-(2-phenyl-2-carboxyethenyl)-4,6-dichloro-1 H-indole-2-carboxylic acid, is a potent and selective inhibitor of [ 3H]glycine binding to the…”
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Binding of the radiolabeled glycine site antagonist [ 3H]MDL 105,519 to homomeric NMDA-NR1a receptors
Published in European journal of pharmacology (03-10-1996)“…We have characterized the binding of [ 3H]MDL 105,519 (( E)-3-(2-phenyl-2-carboxyethenyl)-4,6-dichloro-1 H-indole-2-carboxylic acid), a NMDA receptor glycine…”
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Chemical Development of MDL 103371: An N-Methyl-d-Aspartate-Type Glycine Receptor Antagonist for the Treatment of Stroke
Published in Organic process research & development (01-11-2000)“…MDL 103371 is a N-methyl-d-aspartate (NMDA)-type glycine receptor antagonist for the potential treatment of stroke. Evaluation of five different synthetic…”
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Development of a prototype reporter-based assay for the evaluation of gap junctional intercellular communication
Published in Biotechnology letters (01-10-2001)“…A new reporter-based assay for the evaluation of gap junctional intercellular communication (GJIC) is presented. This assay was applied to the study of…”
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The competitive NMDA antagonist MDL-100,453 reduces infarct size after experimental stroke
Published in Stroke (1970) (01-06-1994)“…The competitive N-methyl-D-aspartate antagonist MDL-100,453 was used to determine whether a neuroprotective effect is demonstrable when the drug is…”
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Enzyme-Activated Antagonists of the Strychnine-Insensitive Glycine/NMDA Receptor
Published in Journal of medicinal chemistry (01-02-1994)Get full text
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Binding of 5H-Dibenzo[a,d]cycloheptene and Dibenz[b,f]oxepin Analogs of Clozapine to Dopamine and Serotonin Receptors
Published in Journal of medicinal chemistry (01-02-1995)“…Series of 5,11-dicarbo- and 11-carbo-5-oxy-10-(1-alkyl-1,2,3,6-tetrahydro-4 pyridinyl) analogues and a 11-carbo-5-oxy-10-(1-methyl-4-piperidinyl) analogue of…”
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2,4-Dihydro-3H-1,2,4-triazol-3-ones as anticonvulsant agents
Published in Journal of medicinal chemistry (01-10-1990)Get full text
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The selectivity of MDL 74,721 in models of neurogenic versus vascular components of migraine
Published in European journal of pharmacology (08-10-1997)“…MDL 74,721 (R)-2-(N1,N1-dipropylamino)-8-methylaminosulfonylmethyl-1,2,3,4-te trahydronaphthalene, a sulfonamidotetralin, has been found to exhibit a…”
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(R)-4-Oxo-5-phosphononorvaline: a new competitive glutamate antagonist at the NMDA receptor complex
Published in Journal of medicinal chemistry (01-11-1990)Get full text
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Preclinical characterization of the potential of the putative atypical antipsychotic MDL 100,907 as a potent 5-HT2A antagonist with a favorable CNS safety profile
Published in The Journal of pharmacology and experimental therapeutics (01-05-1996)“…In preclinical studies, [R-(+)-alpha-(2,3-dimethoxyphenyl)-1-[2-(4-fluorophenyl)ethyl]-4- piperidinemethanol] [formula: see text] (MDL 100,907), a putative…”
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CoMFA, Synthesis, and Pharmacological Evaluation of ( E )-3-(2-Carboxy-2-arylvinyl)-4,6-dichloro-1 H -indole-2-carboxylic Acids: 3-[2-(3-Aminophenyl)-2-carboxyvinyl]-4,6-dichloro-1 H -indole-2-carboxylic Acid, a Potent Selective Glycine-Site NMDA Receptor Antagonist
Published in Journal of medicinal chemistry (01-02-2005)Get full text
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CoMFA, synthesis, and pharmacological evaluation of (E)-3-(2-carboxy-2-arylvinyl)-4,6-dichloro-1H-indole-2-carboxylic acids: 3-[2-(3-Aminophenyl)-2-carboxyvinyl]-4,6-dichloro-1H-indole-2-carboxylic acid, a potent selective glycine-site NMDA receptor antagonis
Published in Journal of medicinal chemistry (2005)Get full text
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