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SSR180711, a Novel Selective α7 Nicotinic Receptor Partial Agonist: (1) Binding and Functional Profile

Neuropsychopharmacology (New York, N.Y.), 2006-10, Vol.32 (1), p.1-16

2006

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SSR180711, a Novel Selective 7 Nicotinic Receptor Partial Agonist: (1) Binding and Functional Profile

Neuropsychopharmacology (New York, N.Y.), 2007-01, Vol.32 (1), p.1-16

2007

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Inhibition by riluzole of electrophysiological responses mediated by rat kainate and NMDA receptors expressed in Xenopus oocytes

European journal of pharmacology, 1993-04, Vol.235 (2), p.283-289

1993

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RPR 119990, a novel alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid antagonist: synthesis, pharmacological properties, and activity in an animal model of amyotrophic lateral sclerosis

The Journal of pharmacology and experimental therapeutics, 2001-10, Vol.299 (1), p.314

2001

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9-Carboxymethyl-5H, 10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one-2-carbocylic acid (RPR117824): Selective anticonvulsive and neuroprotective AMPA antagonist

Bioorganic & medicinal chemistry, 2002-05, Vol.10 (5), p.1627-1637

2002

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From Perception to Consciousness: An Epistemic Vision of Evolutionary Processes

Leonardo (Oxford), 2004-01, Vol.37 (3), p.243-248

Debono, Marc-Williams

2004

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Synthesis and pharmacological properties of 5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one, a new competitive AMPA/KA receptor antagonist

Drug development research, 1999-11, Vol.48 (3), p.121-129

1999

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4,10-Dihydro-4-oxo-4H-imidazo[1,2-a]indeno[1,2-e]pyrazin-2-carboxylic acid derivatives: highly potent and selective AMPA receptors antagonists with in vivo activity

Bioorganic & medicinal chemistry letters, 2000-05, Vol.10 (10), p.1133

2000

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8-methylureido-10-amino-10-methyl-imidazo[1,2-a]indeno[1,2-e] pyrazine-4-ones : Highly in vivo potent and selective AMPA receptor antagonists

Bioorganic & medicinal chemistry, 2000-08, Vol.8 (8), p.2211-2217

2000

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Bioisosteres of 9-carboxymethyl-4-oxo-imidazo[1,2-a]indeno-[1,2-e]pyrazin-2-carboxylic acid derivatives. Progress towards selective, potent in vivo AMPA antagonists with longer durations of action

Bioorganic & medicinal chemistry letters, 2001-01, Vol.11 (2), p.127-132

2001

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8-Methylureido-4,5-dihydro-4-oxo-10H-imidazo[1,2-a]indeno-[1,2-e]pyrazines : Highly potent in vivo AMPA antagonists

Bioorganic & medicinal chemistry letters, 2000-03, Vol.10 (6), p.591-596

2000

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Synthesis and potent anticonvulsant activities of 4-oxo-imidazo[1,2- a]indeno[1,2- e]pyrazin-8- and -9-carboxylic (acetic) acid AMPA antagonists

Bioorganic & medicinal chemistry letters, 2000-12, Vol.10 (24), p.2749-2754

2000

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Synthesis of anticonvulsive AMPA antagonists: 4-Oxo-10-substituted-imidazo[1,2- a]indeno[1,2- e]pyrazin-2-carboxylic acid derivatives

Bioorganic & medicinal chemistry letters, 2001-05, Vol.11 (9), p.1205-1210

2001

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Acute coronary thrombolysis with recombinant human tissue-type plasminogen activator: Initial patency and influence of maintained infusion on reocclusion rate

The American journal of cardiology, 1987-08, Vol.60 (4), p.231-237

1987

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Recombinant tissue-type plasminogen activator and immediate angioplasty in acute myocardial infarction : one-year follow-up

Circulation (New York, N.Y.), 1992-07, Vol.86 (1), p.111-120

1992

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Reasons for the lack of benefit of immediate angioplasty during recombinant tissue plasminogen activator therapy for acute myocardial infarction: A regional wall motion analysis

Journal of the American College of Cardiology, 1991-01, Vol.17 (1), p.11-21

1991

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SSR180711, a Novel Selective α7 Nicotinic Receptor Partial Agonist: (1) Binding and Functional Profile

SSR180711, a novel selective alpha 7 nicotinic receptor partial agonist: (I) binding and functional profile

SSR180711, a Novel Selective 7 Nicotinic Receptor Partial Agonist: (1) Binding and Functional Profile

SSRI80711, a novel selective α7 nicotinic receptor partial agonist: (I) binding and functional profile

SSR180711, a novel selective alpha7 nicotinic receptor partial agonist: (1) binding and functional profile

Inhibition by riluzole of electrophysiological responses mediated by rat kainate and NMDA receptors expressed in Xenopus oocytes

RPR 119990, a novel alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid antagonist: synthesis, pharmacological properties, and activity in an animal model of amyotrophic lateral sclerosis

9-Carboxymethyl-5H, 10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one-2-carbocylic acid (RPR117824): Selective anticonvulsive and neuroprotective AMPA antagonist

From Perception to Consciousness: An Epistemic Vision of Evolutionary Processes

Synthesis and pharmacological properties of 5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one, a new competitive AMPA/KA receptor antagonist

4,10-Dihydro-4-oxo-4H-imidazo[1,2-a]indeno[1,2-e]pyrazin-2-carboxylic acid derivatives: highly potent and selective AMPA receptors antagonists with in vivo activity

8-methylureido-10-amino-10-methyl-imidazo[1,2-a]indeno[1,2-e] pyrazine-4-ones : Highly in vivo potent and selective AMPA receptor antagonists

Bioisosteres of 9-carboxymethyl-4-oxo-imidazo[1,2-a]indeno-[1,2-e]pyrazin-2-carboxylic acid derivatives. Progress towards selective, potent in vivo AMPA antagonists with longer durations of action

8-Methylureido-4,5-dihydro-4-oxo-10H-imidazo[1,2-a]indeno-[1,2-e]pyrazines : Highly potent in vivo AMPA antagonists

Synthesis and potent anticonvulsant activities of 4-oxo-imidazo[1,2- a]indeno[1,2- e]pyrazin-8- and -9-carboxylic (acetic) acid AMPA antagonists

Synthesis of anticonvulsive AMPA antagonists: 4-Oxo-10-substituted-imidazo[1,2- a]indeno[1,2- e]pyrazin-2-carboxylic acid derivatives

Acute coronary thrombolysis with recombinant human tissue-type plasminogen activator: Initial patency and influence of maintained infusion on reocclusion rate

Recombinant tissue-type plasminogen activator and immediate angioplasty in acute myocardial infarction : one-year follow-up

Reasons for the lack of benefit of immediate angioplasty during recombinant tissue plasminogen activator therapy for acute myocardial infarction: A regional wall motion analysis

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