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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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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 GAL3 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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AMPA receptor antagonists

Current medicinal chemistry, 2001-02, Vol.8 (2), p.155-170

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

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

2000

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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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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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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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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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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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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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Novel quenchers for solution phase parallel synthesis

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

1998

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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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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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NR2B selective NMDA receptor antagonists

Current pharmaceutical design, 2002-01, Vol.8 (10), p.845-855

2002

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

Synthetic communications, 2011-12, Vol.41 (23), p.3551-3555

2011

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

Synthetic communications, 2011-12, Vol.41 (23), p.3551-3555

2011

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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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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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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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1-Aminoindanes as novel motif with potential atypical antipsychotic properties

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

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

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

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

AMPA receptor antagonists

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

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

ChemInform Abstract: 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

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

Evolution of schizophrenia drugs: a focus on dopaminergic systems

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

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

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

Novel quenchers for solution phase parallel synthesis

Novel Selective Quinazoline Inhibitors of Endothelin Converting Enzyme-1

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

NR2B selective NMDA receptor antagonists

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

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

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

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

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

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

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