Search Results - "MCCLOSKEY, Timothy C"
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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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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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Effects of the CRF1 receptor antagonist, CP 154,526, in the separation-induced vocalization anxiolytic test in rat pups
Published in Neuropharmacology (01-07-2000)Get full text
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5-Aryl-3-(alkylthio)-4H-1,2,4-triazoles as selective antagonists of strychnine-induced convulsions and potential antispastic agents
Published in Journal of medicinal chemistry (01-01-1994)“…Selected examples from three series of isomeric (alkylthio)-1,2,4-triazoles were prepared and examined for anticonvulsant activity versus strychnine-,…”
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Preclinical characterization of MDL 27,192 as a potential broad spectrum anticonvulsant agent with neuroprotective properties
Published in Epilepsy research (01-04-1997)“…The compound 5-(4-chlorophenyl)-2,4-dihydro-4-ethyl-3H-1,2,4-triazol-3-one (MDL 27,192) was evaluated in a variety of rodent models to assess its…”
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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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5-HT modulation of auditory and visual sensorimotor gating: II. Effects of the 5-HT2A antagonist MDL 100,907 on disruption of sound and light prepulse inhibition produced by 5-HT agonists in Wistar rats
Published in Psychopharmacology (01-03-1996)“…Increasing evidence suggests an important role of 5-HT, and 5-HT2A receptors in particular, in the etiology and treatment of schizophrenia. The prepulse…”
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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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5-HT modulation of auditory and visual sensorimotor gating: I. Effects of 5-HT releasers on sound and light prepulse inhibition in Wistar rats
Published in Psychopharmacology (01-03-1996)“…Increasing evidence suggests an important role for serotonin (5-HT) neurons in the etiology and treatment of schizophrenia. The prepulse inhibition paradigm is…”
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Effects of the CRF 1 receptor antagonist, CP 154,526, in the separation-induced vocalization anxiolytic test in rat pups
Published in Neuropharmacology (2000)“…CRF 1 receptor antagonists have been proposed as novel pharmacological treatments for depression, anxiety and stress disorders. The primary goal of the present…”
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NMDA receptor complex antagonists have potential anxiolytic effects as measured with separation-induced ultrasonic vocalizations
Published in European journal of pharmacology (14-02-1991)“…Pre-weaning rat pups emit ultrasonic vocalizations when removed from the litter. These 'separation-induced vocalizations' (SIV) are suppressed by classical…”
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MDL 100,458 and MDL 102,288: two potent and selective glycine receptor antagonists with different functional profiles
Published in European journal of pharmacology (15-09-1995)“…Glycine receptor antagonists have been proposed to have multiple therapeutic applications, including the treatment of stroke, epilepsy, and anxiety. The…”
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Buspirone effects in an animal conflict procedure: comparison with diazepam and phenobarbital
Published in Pharmacology, biochemistry and behavior (01-05-1987)“…Buspirone has been introduced as a novel non-benzodiazepine anti-anxiety agent. The Conditioned Suppression of Drinking (CSD) paradigm is an "animal model" for…”
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Antagonism of the anti-conflict effects of phenobarbital, but not diazepam, by the A-1 adenosine agonistl-PIA
Published in Psychopharmacology (01-11-1990)Get full text
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Antagonism of the anti-conflict effects of phenobarbital, but not diazepam, by the A-1 adenosine agonist l-PIA
Published in Psychopharmacology (1990)“…The present study examined the effects of the anxiolytics diazepam and phenobarbital, the A-1 adenosine agonist N6-R-phenylisopropyladenosine (l-PIA), and the…”
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beta-Carboline and pentylenetetrazol effects on conflict behavior in the rat
Published in Pharmacology, biochemistry and behavior (01-08-1992)“…The beta-carbolines and the convulsant agent pentylenetetrazol (PTZ) have been reported as "anxiogenic" in several animal models for anxiety. The present study…”
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The effects of beta-antagonists and anxiolytics on conflict behavior in the rat
Published in Pharmacology, biochemistry and behavior (01-03-1989)“…The present studies were designed to evaluate the effects of beta-adrenoceptor antagonists and traditional anxiolytics (phenobarbital and diazepam), alone and…”
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MDL 27,531 reduces spontaneous hindlimb contractions in rats with chronic transections of the spinal cord
Published in Neuroscience letters (23-11-1992)“…Disrupted glycinergic inhibition in the brainstem and spinal cord may contribute to some of the alterations in reflex control seen in patients with spastic…”
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