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NR2B selective NMDA receptor antagonists

Current pharmaceutical design, 2002-01, Vol.8 (10), p.845

2002

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3-Arylimino-2-indolones Are Potent and Selective Galanin GAL3 Receptor Antagonists

Journal of medicinal chemistry, 2006-06, Vol.49 (13), p.3757-3758

2006

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1-Aminoindanes as novel motif with potential atypical antipsychotic properties

Bioorganic & medicinal chemistry, 2008-01, Vol.18 (2), p.489-493

2008

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New Synthesis of Substituted Benzylamines. Novel Application of the Mitsunobu Reaction To Convert Substituted Benzyl Alcohols to Amines

Journal of organic chemistry, 1997-05, Vol.62 (11), p.3754-3757

1997

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Evolution of schizophrenia drugs: a focus on dopaminergic systems

Current opinion in investigational drugs (London, England : 2000), 2008-01, Vol.9 (1), p.37

2008

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Multi- and single-target agents for major psychiatric diseases: therapeutic opportunities and challenges

Current opinion in investigational drugs (London, England : 2000), 2008-01, Vol.9 (1), p.28

2008

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Subtype selective NMDA receptor antagonists: evaluation of some novel alkynyl analogues

Bioorganic & medicinal chemistry letters, 2004-03, Vol.14 (5), p.1213-1216

2004

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Novel Use of Substituted 1,4-Dihydrobenz[d][1,3]oxazin-2-ones in the Synthesis of Important Aminomethyl o-Nitroanilines

Journal of organic chemistry, 1997-12, Vol.62 (26), p.9331-9334

1997

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Design and Synthesis of Novel Quinoxaline-2,3-dione AMPA/GlyN Receptor Antagonists: Amino Acid Derivatives

Journal of medicinal chemistry, 1999-06, Vol.42 (12), p.2266-2271

1999

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AMPA receptor antagonists

Current medicinal chemistry, 2001-02, Vol.8 (2), p.155

2001

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ChemInform Abstract: A Simple Strategy for the Preparation of 6-Substituted 3H-Benzoxazol-2-ones and 3H-Benzothiazol-2-ones

ChemInform, 2012-04, Vol.43 (16), p.no-no

2012

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3-Arylimino-2-indolones Are Potent and Selective Galanin GAL 3 Receptor Antagonists

Journal of medicinal chemistry, 2006-06, Vol.49 (13), p.3757-3758

2006

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3-arylimino-2-indolones are potent and selective galanin GAL3receptor antagonists

Journal of medicinal chemistry, 2006, Vol.49 (13), p.3757-3758

2006

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AMPA receptor agonists, antagonists and modulators: their potential for clinical utility

Expert opinion on therapeutic patents, 1997-10, Vol.7 (10), p.1099-1114

1997

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Synthesis and biological evaluation of substituted 4-(OBz)phenylalanine derivatives as novel N-type calcium channel blockers

Bioorganic & medicinal chemistry letters, 1999-04, Vol.9 (8), p.1121-1126

1999

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Novel quenchers for solution phase parallel synthesis

Tetrahedron letters, 1998-03, Vol.39 (10), p.1121-1124

1998

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Synthesis of novel quinoxaline-5-carboxylic acid derivatives

Journal of heterocyclic chemistry, 1999-09, Vol.36 (5), p.1271-1277

1999

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Design and Synthesis of Novel Quinoxaline-2,3-dione AMPA/Gly N Receptor Antagonists: Amino Acid Derivatives

Journal of medicinal chemistry, 1999-06, Vol.42 (12), p.2266-2271

1999

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Synthesis of hydroxamic acids: [formula omitted] as a new catalyst for the deprotection of O-benzyl hydroxamates

Tetrahedron letters, 1995, Vol.36 (2), p.197-200

1995

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ChemInform Abstract: Synthesis of Novel Quinoxaline-5-carboxylic Acid Derivatives

ChemInform, 2000-04, Vol.31 (14), p.no-no

2000

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Subtype Selective NMDA Receptor Antagonists: Evaluation of Some Novel Alkynyl Analogues

ChemInform, 2004-06, Vol.35 (23), p.no-no

2004

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ChemInform Abstract: Synthesis and Biological Evaluation of Substituted 4-(OBz)Phenylalanine Derivatives as Novel N-Type Calcium Channel Blockers

ChemInform, 1999-08, Vol.30 (33), p.no-no

1999

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Phosphodiesterase 4 inhibition reduces lung fibrosis following targeted type II alveolar epithelial cell injury

Physiological reports, 2018-06, Vol.6 (12), p.e13753-n/a

2018

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Metabolism-Dependent Mutagenicity of a Compound Containing a Piperazinyl Indazole Motif: Role of a Novel P450-Mediated Metabolic Reaction Involving a Putative Oxaziridine Intermediate

Chemical research in toxicology, 2006-10, Vol.19 (10), p.1341-1350

2006

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Novel Selective Quinazoline Inhibitors of Endothelin Converting Enzyme-1

Biochemical and biophysical research communications, 1998-02, Vol.243 (1), p.184-190

1998

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NR2B selective NMDA receptor antagonists

3-Arylimino-2-indolones Are Potent and Selective Galanin GAL3 Receptor Antagonists

1-Aminoindanes as novel motif with potential atypical antipsychotic properties

New Synthesis of Substituted Benzylamines. Novel Application of the Mitsunobu Reaction To Convert Substituted Benzyl Alcohols to Amines

Evolution of schizophrenia drugs: a focus on dopaminergic systems

Multi- and single-target agents for major psychiatric diseases: therapeutic opportunities and challenges

Subtype selective NMDA receptor antagonists: evaluation of some novel alkynyl analogues

Novel Use of Substituted 1,4-Dihydrobenz[d][1,3]oxazin-2-ones in the Synthesis of Important Aminomethyl o-Nitroanilines

Design and Synthesis of Novel Quinoxaline-2,3-dione AMPA/GlyN Receptor Antagonists: Amino Acid Derivatives

AMPA receptor antagonists

ChemInform Abstract: A Simple Strategy for the Preparation of 6-Substituted 3H-Benzoxazol-2-ones and 3H-Benzothiazol-2-ones

3-Arylimino-2-indolones Are Potent and Selective Galanin GAL 3 Receptor Antagonists

3-arylimino-2-indolones are potent and selective galanin GAL3receptor antagonists

AMPA receptor agonists, antagonists and modulators: their potential for clinical utility

Synthesis and biological evaluation of substituted 4-(OBz)phenylalanine derivatives as novel N-type calcium channel blockers

Novel quenchers for solution phase parallel synthesis

Synthesis of novel quinoxaline-5-carboxylic acid derivatives

Design and Synthesis of Novel Quinoxaline-2,3-dione AMPA/Gly N Receptor Antagonists: Amino Acid Derivatives

Synthesis of hydroxamic acids: [formula omitted] as a new catalyst for the deprotection of O-benzyl hydroxamates

ChemInform Abstract: Synthesis of Novel Quinoxaline-5-carboxylic Acid Derivatives

Subtype Selective NMDA Receptor Antagonists: Evaluation of Some Novel Alkynyl Analogues

ChemInform Abstract: Synthesis and Biological Evaluation of Substituted 4-(OBz)Phenylalanine Derivatives as Novel N-Type Calcium Channel Blockers

Phosphodiesterase 4 inhibition reduces lung fibrosis following targeted type II alveolar epithelial cell injury

Metabolism-Dependent Mutagenicity of a Compound Containing a Piperazinyl Indazole Motif: Role of a Novel P450-Mediated Metabolic Reaction Involving a Putative Oxaziridine Intermediate

Novel Selective Quinazoline Inhibitors of Endothelin Converting Enzyme-1

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