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The synthesis and structure–activity relationship of substituted N-phenyl anthranilic acid analogs as amyloid aggregation inhibitors

Bioorganic & medicinal chemistry letters, 2009-02, Vol.19 (3), p.654-657

2009

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2-Amino-4H-3,1-benzoxazin-4-ones as Inhibitors of C1r Serine Protease

Journal of medicinal chemistry, 1998-03, Vol.41 (7), p.1060-1067

1998

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Design and Synthesis of m1-Selective Muscarinic Agonists: (R)-(−)-(Z)-1-Azabicyclo[2.2.1]heptan-3-one, O-(3-(3‘-Methoxyphenyl)-2-propynyl)- oxime Maleate (CI-1017), a Functionally m1-Selective Muscarinic Agonist

Journal of medicinal chemistry, 1998-07, Vol.41 (14), p.2524-2536

1998

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The Discovery and Structure-Activity Relationships of 1,2,3,6-Tetrahydro-4-phenyl-1-[(arylcyclohexenyl)alkyl]pyridines. Dopamine Autoreceptor Agonists and Potential Antipsychotic Agents

Journal of medicinal chemistry, 1994-10, Vol.37 (21), p.3523-3533

1994

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4-(1,2,5,6-Tetrahydro-1-alkyl-3-pyridinyl)-2-thiazolamines: a novel class of compounds with central dopamine agonist properties

Journal of medicinal chemistry, 1990-01, Vol.33 (1), p.311-317

1990

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Kynurenic Acid Derivatives Inhibit the Binding of Nerve Growth Factor (NGF) to the Low-Affinity p75 NGF Receptor

Journal of medicinal chemistry, 1995-10, Vol.38 (22), p.4439-4445

1995

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Evaluation of the effects of the enantiomers of reduced haloperidol, azaperol, and related 4-amino-1-arylbutanols on dopamine and .sigma. receptors

Journal of medicinal chemistry, 1993-11, Vol.36 (24), p.3929-3936

1993

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Identification of a 3-Hydroxylated Tacrine Metabolite in Rat and Man: Metabolic Profiling Implications and Pharmacology

Journal of medicinal chemistry, 1996-07, Vol.39 (15), p.3014-3018

1996

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Dopamine autoreceptor agonists as potential antipsychotics. 3. 6-Propyl-4,5,5a,6,7,8-hexahydrothiazolo[4,5-f]quinolin-2-amine

Journal of medicinal chemistry, 1991-09, Vol.34 (9), p.2736-2746

1991

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Amnesia-reversal activity of a series of cyclic imides

Journal of medicinal chemistry, 1987-03, Vol.30 (3), p.498-503

1987

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Nitrones by heterolytic fragmentation of .gamma.-N-hydroxyamino sulfonates. Conversion of a decahydroquinoline to a perhydroazaazulene

Journal of organic chemistry, 1985-10, Vol.50 (20), p.3938-3940

1985

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Synthesis and evaluation of 2-aryl-4H-3,1-benzoxazin-4-ones as C1r serine protease inhibitors

Bioorganic & medicinal chemistry letters, 1996-03, Vol.6 (6), p.679-682

1996

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2-Amino-4 H -3,1-benzoxazin-4-ones as Inhibitors of C1r Serine Protease

Journal of medicinal chemistry, 1998-03, Vol.41 (7), p.1060-1067

1998

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Synthesis of the enantiomers of reduced haloperidol

Pharmaceutical research, 1991-08, Vol.8 (8), p.1002-1005

1991

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EFFICIENT SYNTHESIS OF EXO-1-AZABICYCLO[2.2.1]HEPTAN-3-OL

Organic preparations and procedures international, 1997-06, Vol.29 (3), p.330-335

1997

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Synthesis and pharmacological evaluation of the enantiomers of the dopamine autoreceptor agonist PD 135385

Bioorganic & medicinal chemistry letters, 1993-04, Vol.3 (4), p.639-644

1993

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Synthesis and dopaminergic activity of the enantiomers of 6-methyl-4,5a,6,7,8-hexahydrothiazolo[4,5-f]quinolin-2-amine (PD 128483)

Bioorganic & medicinal chemistry letters, 1991, Vol.1 (10), p.539-544

1991

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Novel 4,5,6,7-tetrahydrobenzothiazole dopamine agonists display very low stereoselectivity in their interaction with dopamine receptors

Bioorganic & medicinal chemistry letters, 1991, Vol.1 (4), p.189-192

1991

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The design and synthesis of sulfonamides as caspase-1 inhibitors

Bioorganic & medicinal chemistry letters, 2004-02, Vol.14 (3), p.809-812

2004

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The synthesis and structure–activity relationship of substituted N-phenyl anthranilic acid analogs as amyloid aggregation inhibitors

2-Amino-4H-3,1-benzoxazin-4-ones as Inhibitors of C1r Serine Protease

Design and Synthesis of m1-Selective Muscarinic Agonists: (R)-(−)-(Z)-1-Azabicyclo[2.2.1]heptan-3-one, O-(3-(3‘-Methoxyphenyl)-2-propynyl)- oxime Maleate (CI-1017), a Functionally m1-Selective Muscarinic Agonist

The Discovery and Structure-Activity Relationships of 1,2,3,6-Tetrahydro-4-phenyl-1-[(arylcyclohexenyl)alkyl]pyridines. Dopamine Autoreceptor Agonists and Potential Antipsychotic Agents

4-(1,2,5,6-Tetrahydro-1-alkyl-3-pyridinyl)-2-thiazolamines: a novel class of compounds with central dopamine agonist properties

Kynurenic Acid Derivatives Inhibit the Binding of Nerve Growth Factor (NGF) to the Low-Affinity p75 NGF Receptor

Evaluation of the effects of the enantiomers of reduced haloperidol, azaperol, and related 4-amino-1-arylbutanols on dopamine and .sigma. receptors

Identification of a 3-Hydroxylated Tacrine Metabolite in Rat and Man: Metabolic Profiling Implications and Pharmacology

Dopamine autoreceptor agonists as potential antipsychotics. 3. 6-Propyl-4,5,5a,6,7,8-hexahydrothiazolo[4,5-f]quinolin-2-amine

Amnesia-reversal activity of a series of cyclic imides

Nitrones by heterolytic fragmentation of .gamma.-N-hydroxyamino sulfonates. Conversion of a decahydroquinoline to a perhydroazaazulene

Synthesis and evaluation of 2-aryl-4H-3,1-benzoxazin-4-ones as C1r serine protease inhibitors

2-Amino-4 H -3,1-benzoxazin-4-ones as Inhibitors of C1r Serine Protease

Synthesis of the enantiomers of reduced haloperidol

EFFICIENT SYNTHESIS OF EXO-1-AZABICYCLO[2.2.1]HEPTAN-3-OL

Synthesis and pharmacological evaluation of the enantiomers of the dopamine autoreceptor agonist PD 135385

Synthesis and dopaminergic activity of the enantiomers of 6-methyl-4,5a,6,7,8-hexahydrothiazolo[4,5-f]quinolin-2-amine (PD 128483)

Novel 4,5,6,7-tetrahydrobenzothiazole dopamine agonists display very low stereoselectivity in their interaction with dopamine receptors

The design and synthesis of sulfonamides as caspase-1 inhibitors

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