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Dinitrobenzene-Mediated Production of Peroxynitrite by Neuronal Nitric Oxide Synthase

Chemical research in toxicology, 2002-07, Vol.15 (7), p.927-934

Miller, R. Timothy

2002

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Boc-CCK-4 derivatives containing side-chain ureas as potent and selective CCK-A receptor agonists

Journal of medicinal chemistry, 1991-09, Vol.34 (9), p.2837-2842

1991

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Tetrapeptide CCK-A Agonists: Effect of Backbone N-Methylations on in vitro and in vivo CCK Activity

Journal of medicinal chemistry, 1994-03, Vol.37 (5), p.630-635

1994

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Development of potent and selective CCK-A receptor agonists from Boc-CCK-4: tetrapeptides containing Lys(N.epsilon.)-amide residues

Journal of medicinal chemistry, 1992-05, Vol.35 (11), p.2007-2014

1992

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Enhanced robotic dissolution system with concurrent off-line analysis

Journal of pharmaceutical and biomedical analysis, 1993-10, Vol.11 (10), p.861-869

1993

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CCK-A-Selective Tetrapeptides Containing Lys(N.epsilon.)-Amide Residues: Favorable in vivo and in vitro Effects of N-Methylation at the Aspartyl Residue

Journal of medicinal chemistry, 1994-05, Vol.37 (11), p.1569-1571

1994

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Effects of Intracerebroventricular Administration of 5-(Glutathion-S-yl)-α-methyldopamine on Brain Dopamine, Serotonin, and Norepinephrine Concentrations in Male Sprague-Dawley Rats

Chemical research in toxicology, 1996-03, Vol.9 (2), p.457-465

1996

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Metabolism of 5-(Glutathion-S-yl)-.alpha.-methyldopamine following Intracerebroventricular Administration to Male Sprague-Dawley Rats

Chemical research in toxicology, 1995-07, Vol.8 (5), p.634-641

1995

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A Probe for Sequence-Dependent Nucleic Acid Dynamics

Journal of the American Chemical Society, 1995-09, Vol.117 (36), p.9377-9378

1995

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Novel Asp32-Replacement Tetrapeptide Analogs as Potent and Selective CCK-A Agonists

Journal of medicinal chemistry, 1994-05, Vol.37 (11), p.1562-1568

1994

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Interfacial analysis techniques

Current opinion in colloid & interface science, 2014-06, Vol.19 (3), p.175-175

2014

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A Study of the Conversion of Para-substituted Methylene-bis-arylamines and Trimeric Methylene-arylamines to Substituted 2-Aminobenzylarylamines

Journal of the American Chemical Society, 1938-08, Vol.60 (8), p.1738-1741

1938

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Bubble and Drop Interfaces

1, 2011

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Colloid and Interface Chemistry for Nanotechnology

1, 2014

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Toward the synthesis of a second-generation nitroxide spin probe for DNA dynamics studies: Modified oligonucleotides

Bioorganic & medicinal chemistry letters, 1994, Vol.4 (8)

1994

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Structure–Activity relationships of non-imidazole H 3 Receptor ligands. Part 2: binding preference for d-Amino acids motifs

Bioorganic & medicinal chemistry letters, 2002-08, Vol.12 (15), p.2035-2037

2002

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Structure–activity relationships of non-imidazole H 3 receptor ligands. Part 1

Bioorganic & medicinal chemistry letters, 2002-08, Vol.12 (15), p.2031-2034

2002

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Computational Methods for Complex Liquid-Fluid Interfaces

1, 2015

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Assay procedures for ascorbic acid 2-sulfate sulfohydrolase

Analytical biochemistry, 1977-05, Vol.79 (1), p.23-32

1977

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Structure–activity relationships of non-imidazole H 3 receptor ligands. Part 3: 5-Substituted 3-phenyl-1,2,4-oxadiazoles as potent antagonists

Bioorganic & medicinal chemistry letters, 2004-02, Vol.14 (3), p.673-676

2004

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Annual Reports in Organic Synthesis -- 1970

1, 1971

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Tetrapeptide CCK agonists : structure-activity studies on modification at the N-terminus

Journal of medicinal chemistry, 1994, Vol.37 (2), p.309-313

1994

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Toward the synthesis of a second-generation nitroxide spin probe for DNA dynamics studies

Bioorganic & medicinal chemistry letters, 1994-04, Vol.4 (8), p.981-986

1994

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trans-3-n-propyl-L-proline is a highly favorable, conformationally restricted replacement for methionine in the C-terminal tetrapeptide of cholecystokinin. Stereoselective synthesis of 3-allyl- and 3-n-propyul-L-proline derivatives from 4-hydroxy-L-proline

Journal of medicinal chemistry, 1991, Vol.34 (1), p.455-457

1991

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Drop and bubble shape analysis as a tool for dilational rheological studies of interfacial layers

Novel Methods to Study Interfacial Layers, 2001, Vol.11, p.439-483

2001

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Dinitrobenzene-Mediated Production of Peroxynitrite by Neuronal Nitric Oxide Synthase

Boc-CCK-4 derivatives containing side-chain ureas as potent and selective CCK-A receptor agonists

Tetrapeptide CCK-A Agonists: Effect of Backbone N-Methylations on in vitro and in vivo CCK Activity

Development of potent and selective CCK-A receptor agonists from Boc-CCK-4: tetrapeptides containing Lys(N.epsilon.)-amide residues

Enhanced robotic dissolution system with concurrent off-line analysis

CCK-A-Selective Tetrapeptides Containing Lys(N.epsilon.)-Amide Residues: Favorable in vivo and in vitro Effects of N-Methylation at the Aspartyl Residue

Effects of Intracerebroventricular Administration of 5-(Glutathion-S-yl)-α-methyldopamine on Brain Dopamine, Serotonin, and Norepinephrine Concentrations in Male Sprague-Dawley Rats

Metabolism of 5-(Glutathion-S-yl)-.alpha.-methyldopamine following Intracerebroventricular Administration to Male Sprague-Dawley Rats

A Probe for Sequence-Dependent Nucleic Acid Dynamics

Novel Asp32-Replacement Tetrapeptide Analogs as Potent and Selective CCK-A Agonists

Interfacial analysis techniques

A Study of the Conversion of Para-substituted Methylene-bis-arylamines and Trimeric Methylene-arylamines to Substituted 2-Aminobenzylarylamines

Bubble and Drop Interfaces

Colloid and Interface Chemistry for Nanotechnology

Toward the synthesis of a second-generation nitroxide spin probe for DNA dynamics studies: Modified oligonucleotides

Structure–Activity relationships of non-imidazole H 3 Receptor ligands. Part 2: binding preference for d-Amino acids motifs

Structure–activity relationships of non-imidazole H 3 receptor ligands. Part 1

Computational Methods for Complex Liquid-Fluid Interfaces

Assay procedures for ascorbic acid 2-sulfate sulfohydrolase

Structure–activity relationships of non-imidazole H 3 receptor ligands. Part 3: 5-Substituted 3-phenyl-1,2,4-oxadiazoles as potent antagonists

Annual Reports in Organic Synthesis -- 1970

Tetrapeptide CCK agonists : structure-activity studies on modification at the N-terminus

Toward the synthesis of a second-generation nitroxide spin probe for DNA dynamics studies

trans-3-n-propyl-L-proline is a highly favorable, conformationally restricted replacement for methionine in the C-terminal tetrapeptide of cholecystokinin. Stereoselective synthesis of 3-allyl- and 3-n-propyul-L-proline derivatives from 4-hydroxy-L-proline

Drop and bubble shape analysis as a tool for dilational rheological studies of interfacial layers

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