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High-Affinity Partial Agonist Imidazo[1,5-a]quinoxaline Amides, Carbamates, and Ureas at the γ-Aminobutyric Acid A/Benzodiazepine Receptor Complex

Journal of medicinal chemistry, 1996-01, Vol.39 (1), p.158-175

1996

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Azulenyl Nitrones: Colorimetric Detection of Oxyradical End Products and Neuroprotection in the Gerbil Transient Forebrain Ischemia/Reperfusion Model

Free radical biology & medicine, 1998-03, Vol.24 (5), p.738-744

1998

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Pharmacology of U-91356A, an agonist for the dopamine D2 receptor subtype

European journal of pharmacology, 1996-12, Vol.317 (1), p.29-38

1996

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Piperazine Imidazo[1,5-a]quinoxaline Ureas as High-Affinity GABAA Ligands of Dual Functionality

Journal of medicinal chemistry, 1999-04, Vol.42 (7), p.1123-1144

1999

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Two imidazoquinoxaline ligands for the benzodiazepine site sharing a second low affinity site on rat GABAA receptors but with the opposite functionality

British journal of pharmacology, 1998-04, Vol.123 (8), p.1490-1494

1998

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Dopaminergic and serotonergic activities of imidazoquinolinones and related compounds

Journal of medicinal chemistry, 1992-03, Vol.35 (6), p.1076-1092

1992

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3-Phenyl-Substituted Imidazo[1,5-a]quinoxalin-4-ones and Imidazo[1,5-a]quinoxaline Ureas That Have High Affinity at the GABAA/Benzodiazepine Receptor Complex

Journal of medicinal chemistry, 1996-09, Vol.39 (19), p.3820-3836

1996

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3-Phenyl-Substituted Imidazo[1,5- a ]quinoxalin-4-ones and Imidazo[1,5- a ]quinoxaline Ureas That Have High Affinity at the GABA A /Benzodiazepine Receptor Complex

Journal of medicinal chemistry, 1996-09, Vol.39 (19), p.3820-3836

1996

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Centrally acting serotonergic agents. Synthesis and structure-activity relationships of C-1- or C-3-substituted derivatives of 8-hydroxy-2-(di-n-propylamino)tetralin

Journal of medicinal chemistry, 1993-03, Vol.36 (6), p.671-682

1993

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Regioselective and stereoselective syntheses of 1,2,3-triaminocyclohexane derivatives

Journal of organic chemistry, 1993-07, Vol.58 (15), p.4043-4048

1993

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Piperazine Imidazo[1,5- a ]quinoxaline Ureas as High-Affinity GABA A Ligands of Dual Functionality

Journal of medicinal chemistry, 1999-04, Vol.42 (7), p.1123-1144

1999

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Naphtho and benzo analogs of the .kappa. opioid agonist trans-(.+-.)-3,4-dichloro-N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl]benzeneacetamide

Journal of medicinal chemistry, 1991-06, Vol.34 (6), p.1891-1896

1991

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Pharmacological characterization of U-101387, a dopamine D4 receptor selective antagonist

The Journal of pharmacology and experimental therapeutics, 1996-12, Vol.279 (3), p.1392

1996

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Synthetic Studies towards A trans-3,4-Diamine Derivative of Piperidine Mimicking Buspirone

Heterocycles, 1994-12, Vol.39 (1), p.163

1994

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Effects of Lazaroids And A Peroxynitrite Scavenger In A Cell Model Of Peroxynitrite Toxicity

Free radical biology & medicine, 1997, Vol.22 (1), p.223-228

1997

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4-Amino-4-arylcyclohexanones and their derivatives: a novel class of analgesics. 2. Modification of the carbonyl function

Journal of medicinal chemistry, 1981-04, Vol.24 (4), p.404-408

1981

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4-(p-Bromophenyl)-4-(dimethylamino)-1-phenethylcyclohexanol, an extremely potent representative of a new analgesic series

Journal of medicinal chemistry, 1979-10, Vol.22 (10), p.1157-1158

1979

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8-Chloro-1-methyl-6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepines with substituents at C-4

Journal of medicinal chemistry, 1980-06, Vol.23 (6), p.643-647

1980

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Pharmacology of U-91356A, an agonist for the dopamine D 2 receptor subtype

European journal of pharmacology, 1996-12, Vol.317 (1), p.29-38

1996

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Two imidazoquinoxaline ligands for the benzodiazepine site sharing a second low affinity site on rat GABA(A) receptors but with the opposite functionality

British journal of pharmacology, 1998-04, Vol.123 (8), p.1490-1494

1998

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The use of salicylate hydroxylation to detect hydroxyl radical generation in ischemic and traumatic brain injury : reversal by tirilazad mesylate (U-74006F)

Molecular and chemical neuropathology, 1993-10, Vol.20 (2), p.147-162

1993

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Comparison of pyrrolidinyl and piperidinyl benzamides for their anticonvulsant activity and inhibitory action on sodium channel

British journal of pharmacology, 1992-05, Vol.106 (1), p.49-54

1992

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Differential affinity of dihydroimidazoquinoxalines and diimidazoquinazolines to the α1β2γ2 and α6β2γ2 subtypes of cloned GABAA receptors

British journal of pharmacology, 1993-10, Vol.110 (2), p.677-680

1993

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Triazolobenzodiazepines: A new class of stimulators of tissue-type plasminogen activator synthesis in human endothelial cells

Biochemical pharmacology, 1993-07, Vol.46 (1), p.61-67

1993

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Inhibition of cyclic flow variations and reocclusion after thrombolysis in dogs by a novel antagonist of platelet-activating factor

Journal of the American College of Cardiology, 1991-12, Vol.18 (7), p.1804-1810

1991

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High-Affinity Partial Agonist Imidazo[1,5-a]quinoxaline Amides, Carbamates, and Ureas at the γ-Aminobutyric Acid A/Benzodiazepine Receptor Complex

Azulenyl Nitrones: Colorimetric Detection of Oxyradical End Products and Neuroprotection in the Gerbil Transient Forebrain Ischemia/Reperfusion Model

Pharmacology of U-91356A, an agonist for the dopamine D2 receptor subtype

Piperazine Imidazo[1,5-a]quinoxaline Ureas as High-Affinity GABAA Ligands of Dual Functionality

Two imidazoquinoxaline ligands for the benzodiazepine site sharing a second low affinity site on rat GABAA receptors but with the opposite functionality

Dopaminergic and serotonergic activities of imidazoquinolinones and related compounds

3-Phenyl-Substituted Imidazo[1,5-a]quinoxalin-4-ones and Imidazo[1,5-a]quinoxaline Ureas That Have High Affinity at the GABAA/Benzodiazepine Receptor Complex

3-Phenyl-Substituted Imidazo[1,5- a ]quinoxalin-4-ones and Imidazo[1,5- a ]quinoxaline Ureas That Have High Affinity at the GABA A /Benzodiazepine Receptor Complex

Centrally acting serotonergic agents. Synthesis and structure-activity relationships of C-1- or C-3-substituted derivatives of 8-hydroxy-2-(di-n-propylamino)tetralin

Regioselective and stereoselective syntheses of 1,2,3-triaminocyclohexane derivatives

Piperazine Imidazo[1,5- a ]quinoxaline Ureas as High-Affinity GABA A Ligands of Dual Functionality

Naphtho and benzo analogs of the .kappa. opioid agonist trans-(.+-.)-3,4-dichloro-N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl]benzeneacetamide

Pharmacological characterization of U-101387, a dopamine D4 receptor selective antagonist

Synthetic Studies towards A trans-3,4-Diamine Derivative of Piperidine Mimicking Buspirone

Effects of Lazaroids And A Peroxynitrite Scavenger In A Cell Model Of Peroxynitrite Toxicity

4-Amino-4-arylcyclohexanones and their derivatives: a novel class of analgesics. 2. Modification of the carbonyl function

4-(p-Bromophenyl)-4-(dimethylamino)-1-phenethylcyclohexanol, an extremely potent representative of a new analgesic series

8-Chloro-1-methyl-6-phenyl-4H-s-triazolo[4,3-a][1,4]benzodiazepines with substituents at C-4

Pharmacology of U-91356A, an agonist for the dopamine D 2 receptor subtype

Two imidazoquinoxaline ligands for the benzodiazepine site sharing a second low affinity site on rat GABA(A) receptors but with the opposite functionality

The use of salicylate hydroxylation to detect hydroxyl radical generation in ischemic and traumatic brain injury : reversal by tirilazad mesylate (U-74006F)

Comparison of pyrrolidinyl and piperidinyl benzamides for their anticonvulsant activity and inhibitory action on sodium channel

Differential affinity of dihydroimidazoquinoxalines and diimidazoquinazolines to the α1β2γ2 and α6β2γ2 subtypes of cloned GABAA receptors

Triazolobenzodiazepines: A new class of stimulators of tissue-type plasminogen activator synthesis in human endothelial cells

Inhibition of cyclic flow variations and reocclusion after thrombolysis in dogs by a novel antagonist of platelet-activating factor

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