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Novel Inhibitors of Cytokine-induced IκBα Phosphorylation and Endothelial Cell Adhesion Molecule Expression Show Anti-inflammatory Effects in Vivo

The Journal of biological chemistry, 1997-08, Vol.272 (34), p.21096-21103

1997

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Indanylacetic Acid Derivatives Carrying 4-Thiazolyl-phenoxy Tail Groups, a New Class of Potent PPAR α/γ/δ Pan Agonists: Synthesis, Structure−Activity Relationship, and In Vivo Efficacy

Journal of medicinal chemistry, 2007-03, Vol.50 (5), p.984-1000

2007

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A novel estrogen receptor ligand template

Bioorganic & medicinal chemistry letters, 2003-06, Vol.13 (11), p.1919-1922

2003

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1-Phenyl-5-pyrazolyl ureas: potent and selective p38 kinase inhibitors

Bioorganic & medicinal chemistry letters, 2000-09, Vol.10 (18), p.2051-2054

2000

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Discovery of a new class of p38 kinase inhibitors

Bioorganic & medicinal chemistry letters, 2000-09, Vol.10 (18), p.2047-2050

2000

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Bilin attachment sites in the alpha and beta subunits of B-phycoerythrin. Structural studies on a doubly peptide-linked phycoerythrobilin

The Journal of biological chemistry, 1984-05, Vol.259 (9), p.5481-5484

1984

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Phycobiliprotein-bilin linkage diversity. I. Structural studies on A- and D-ring-linked phycocyanobilins

The Journal of biological chemistry, 1986-05, Vol.261 (15), p.6790-6796

1986

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A-77636 : a potent and selective dopamine D1 receptor agonist with antiparkinsonian activity in marmosets

European journal of pharmacology, 1992-12, Vol.229 (2-3), p.203-209

1992

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Synthesis and pharmacological characterization of a potent, orally active p38 kinase inhibitor

Bioorganic & medicinal chemistry letters, 2002-06, Vol.12 (12), p.1559-1562

2002

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Photochemical Release of Amines by C,N-Bond Cleavage

Synlett, 2003, Vol.2003 (4), p.501-504

2003

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A68930: A Potent and Specific Agonist for the D-1 Dopamine Receptor

American journal of hypertension, 1990-06, Vol.3 (6-Pt-2), p.40S-42S

1990

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Bilin attachment sites in the alpha and beta subunits of B-phycoerythrin. Structural studies on the singly linked phycoerythrobilins

The Journal of biological chemistry, 1984-05, Vol.259 (9), p.5485-5489

1984

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Synthesis and dopaminergic activity of 3-substituted 1-(aminomethyl)-3,4-dihydro-5,6-dihydroxy-1H-2-benzopyrans: characterization of an auxiliary binding region in the D1 receptor

Journal of medicinal chemistry, 1991-08, Vol.34 (8), p.2561-2569

1991

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A68930: a potent agonist selective for the dopamine D1 receptor

European journal of pharmacology, 1991-06, Vol.199 (2), p.209-219

1991

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Novel inhibitors of cytokine-induced IkappaBalpha phosphorylation and endothelial cell adhesion molecule expression show anti-inflammatory effects in vivo

The Journal of biological chemistry, 1997-08, Vol.272 (34), p.21096-21103

1997

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(1R,3S)-1-(Aminomethyl)-3,4-dihydro-5,6-dihydroxy-3-phenyl-1H-2-benzopyran: a potent and selective D1 agonist

Journal of medicinal chemistry, 1990-11, Vol.33 (11), p.2948-2950

1990

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Synthesis and pharmacological evaluation of 1-(aminomethyl)-3,4-dihydro-5-hydroxy-1H-2-benzopyrans as dopamine D1 selective ligands

Journal of medicinal chemistry, 1991-10, Vol.34 (10), p.2946-2953

1991

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A68930 : a potent agonist specific for the dopamine D1 receptor

Neurochemistry international, 1992-03, Vol.20 (MAR), p.157S-160S

1992

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A-77636: A potent and selective dopamine D sub(1) receptor agonist with antiparkinsonian activity in marmosets

European journal of pharmacology, 1992-01, Vol.229 (2-3), p.203-209

1992

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(1R,3S)-1-(Aminomethyl)-3,4-dihydro-5,6-di-hydroxy-3-phenyl-1H-2-benzopyran : a potent and selective D1 agonist

Journal of medicinal chemistry, 1990, Vol.33 (11), p.2948-2950

1990

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A 77636, A DOPAMINE (DA) D-1 RECEPTOR AGONIST WITH EFFICACY IN THE MPTP MARMOSET MODEL OF PARKINSONISM

Clinical neuropharmacology, 1992, Vol.15, p.601

1992

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Preparation of an affinity chromatography matrix for the selective purification of the dopamine D2 receptor from bovine striatal membranes

Biochimica et biophysica acta, 1989-11, Vol.986 (2), p.271-280

1989

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A68930: A potent agonist selective for the dopamine D sub(1) receptor

European journal of pharmacology, 1991-01, Vol.199 (2), p.209-219

1991

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A68930 : a potent agonist selective for the dopamikne D1 receptor

European journal of pharmacology, 1991, Vol.199 (2), p.209-219

1991

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Relative stereochemistry of the A ring of plant bile pigments

Journal of the American Chemical Society, 1984-05, Vol.106 (9), p.2645-2651

1984

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Novel Inhibitors of Cytokine-induced IκBα Phosphorylation and Endothelial Cell Adhesion Molecule Expression Show Anti-inflammatory Effects in Vivo

Indanylacetic Acid Derivatives Carrying 4-Thiazolyl-phenoxy Tail Groups, a New Class of Potent PPAR α/γ/δ Pan Agonists: Synthesis, Structure−Activity Relationship, and In Vivo Efficacy

A novel estrogen receptor ligand template

1-Phenyl-5-pyrazolyl ureas: potent and selective p38 kinase inhibitors

Discovery of a new class of p38 kinase inhibitors

Bilin attachment sites in the alpha and beta subunits of B-phycoerythrin. Structural studies on a doubly peptide-linked phycoerythrobilin

Phycobiliprotein-bilin linkage diversity. I. Structural studies on A- and D-ring-linked phycocyanobilins

A-77636 : a potent and selective dopamine D1 receptor agonist with antiparkinsonian activity in marmosets

Synthesis and pharmacological characterization of a potent, orally active p38 kinase inhibitor

Photochemical Release of Amines by C,N-Bond Cleavage

A68930: A Potent and Specific Agonist for the D-1 Dopamine Receptor

Bilin attachment sites in the alpha and beta subunits of B-phycoerythrin. Structural studies on the singly linked phycoerythrobilins

Synthesis and dopaminergic activity of 3-substituted 1-(aminomethyl)-3,4-dihydro-5,6-dihydroxy-1H-2-benzopyrans: characterization of an auxiliary binding region in the D1 receptor

A68930: a potent agonist selective for the dopamine D1 receptor

Novel inhibitors of cytokine-induced IkappaBalpha phosphorylation and endothelial cell adhesion molecule expression show anti-inflammatory effects in vivo

(1R,3S)-1-(Aminomethyl)-3,4-dihydro-5,6-dihydroxy-3-phenyl-1H-2-benzopyran: a potent and selective D1 agonist

Synthesis and pharmacological evaluation of 1-(aminomethyl)-3,4-dihydro-5-hydroxy-1H-2-benzopyrans as dopamine D1 selective ligands

A68930 : a potent agonist specific for the dopamine D1 receptor

A-77636: A potent and selective dopamine D sub(1) receptor agonist with antiparkinsonian activity in marmosets

(1R,3S)-1-(Aminomethyl)-3,4-dihydro-5,6-di-hydroxy-3-phenyl-1H-2-benzopyran : a potent and selective D1 agonist

A 77636, A DOPAMINE (DA) D-1 RECEPTOR AGONIST WITH EFFICACY IN THE MPTP MARMOSET MODEL OF PARKINSONISM

Preparation of an affinity chromatography matrix for the selective purification of the dopamine D2 receptor from bovine striatal membranes

A68930: A potent agonist selective for the dopamine D sub(1) receptor

A68930 : a potent agonist selective for the dopamikne D1 receptor

Relative stereochemistry of the A ring of plant bile pigments

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