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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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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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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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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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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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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

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

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

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

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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