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CoMFA, Synthesis, and Pharmacological Evaluation of (E)-3-(2-Carboxy-2-arylvinyl)-4,6-dichloro-1H-indole-2-carboxylic Acids: 3-[2-(3-Aminophenyl)-2-carboxyvinyl]-4,6-dichloro-1H-indole-2-carboxylic Acid, a Potent Selective Glycine-Site NMDA Receptor Antagonist

Journal of medicinal chemistry, 2005-02, Vol.48 (4), p.995-1018

2005

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3-(2-Carboxyindol-3-yl)propionic acid derivatives: antagonists of the strychnine-insensitive glycine receptor associated with the N-methyl-D-aspartate receptor complex

Journal of medicinal chemistry, 1990-11, Vol.33 (11), p.2944-2946

1990

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3-(2-Carboxyindol-3-yl)propionic acid-based antagonists of the NMDA (N-methyl-D-aspartic acid) receptor associated glycine binding site

Journal of medicinal chemistry, 1992-05, Vol.35 (10), p.1791-1799

1992

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CoMFA, Synthesis, and Pharmacological Evaluation of ( E )-3-(2-Carboxy-2-arylvinyl)-4,6-dichloro-1 H -indole-2-carboxylic Acids: 3-[2-(3-Aminophenyl)-2-carboxyvinyl]-4,6-dichloro-1 H -indole-2-carboxylic Acid, a Potent Selective Glycine-Site NMDA Receptor Antagonist

Journal of medicinal chemistry, 2005-02, Vol.48 (4), p.995-1018

2005

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CoMFA, synthesis, and pharmacological evaluation of (E)-3-(2-carboxy-2-arylvinyl)-4,6-dichloro-1H-indole-2-carboxylic acids: 3-[2-(3-Aminophenyl)-2-carboxyvinyl]-4,6-dichloro-1H-indole-2-carboxylic acid, a potent selective glycine-site NMDA receptor antagonis

Journal of medicinal chemistry, 2005, Vol.48 (4), p.995-1018

2005

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3-(2-Carboxyindol-3-yl)propionic acid-based antagonists of the N-methyl-D-aspartic acid receptor associated glycine binding site

Journal of medicinal chemistry, 1992-05, Vol.35 (10), p.1791-1799

1992

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Inhibition of steroid 5α-reductase by “inverted”, competitive inhibitors

Bioorganic & medicinal chemistry letters, 1994-03, Vol.4 (6), p.847-851

1994

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Synthesis of 3( [formula omitted])-phosphonoacetyl-2( [formula omitted])-piperidinecarboxylic acid, a conformationally-restricted glutamate antagonist

Bioorganic & medicinal chemistry letters, 1991, Vol.1 (9), p.441-444

1991

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Synthesis and biological activity of sulfoximine-modified myristic acid analogues

Bioorganic & medicinal chemistry letters, 1993-08, Vol.3 (8), p.1717-1722

1993

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Syntheses of [formula omitted]-2-fluoromethy- [formula omitted]-tyrosine and [formula omitted]-2-difluoromethyl- [formula omitted]-tyrosine as potential inhibitors of tyrosine hydroxylase

Tetrahedron letters, 1991-02, Vol.32 (7), p.887-890

1991

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Superagonist, Full Agonist, Partial Agonist, and Antagonist Actions of Arylguanidines at 5‑Hydroxytryptamine‑3 (5-HT3) Subunit A Receptors

ACS chemical neuroscience, 2016-11, Vol.7 (11), p.1565-1574

2016

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“Methylene Bridge” to 5‑HT3 Receptor Antagonists: Conformationally Constrained Phenylguanidines

ACS chemical neuroscience, 2019-03, Vol.10 (3), p.1380-1389

2019

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"Methylene Bridge" to 5-HT 3 Receptor Antagonists: Conformationally Constrained Phenylguanidines

ACS chemical neuroscience, 2019-03, Vol.10 (3), p.1380-1389

2019

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Theorizing the Americanist tradition

Theorizing the Americanist tradition, 1999, Vol.13.

1, 1999

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CoMFA, Synthesis, and Pharmacological Evaluation of (E)-3-(2-Carboxy-2-arylvinyl)-4,6-dichloro-1H-indole-2-carboxylic Acids: 3-[2-(3-Aminophenyl)-2-carboxyvinyl]-4,6-dichloro-1H-indole-2-carboxylic Acid, a Potent Selective Glycine-Site NMDA Receptor Antagonist

3-(2-Carboxyindol-3-yl)propionic acid derivatives: antagonists of the strychnine-insensitive glycine receptor associated with the N-methyl-D-aspartate receptor complex

3-(2-Carboxyindol-3-yl)propionic acid-based antagonists of the NMDA (N-methyl-D-aspartic acid) receptor associated glycine binding site

CoMFA, Synthesis, and Pharmacological Evaluation of ( E )-3-(2-Carboxy-2-arylvinyl)-4,6-dichloro-1 H -indole-2-carboxylic Acids: 3-[2-(3-Aminophenyl)-2-carboxyvinyl]-4,6-dichloro-1 H -indole-2-carboxylic Acid, a Potent Selective Glycine-Site NMDA Receptor Antagonist

CoMFA, synthesis, and pharmacological evaluation of (E)-3-(2-carboxy-2-arylvinyl)-4,6-dichloro-1H-indole-2-carboxylic acids: 3-[2-(3-Aminophenyl)-2-carboxyvinyl]-4,6-dichloro-1H-indole-2-carboxylic acid, a potent selective glycine-site NMDA receptor antagonis

3-(2-Carboxyindol-3-yl)propionic acid-based antagonists of the N-methyl-D-aspartic acid receptor associated glycine binding site

Inhibition of steroid 5α-reductase by “inverted”, competitive inhibitors

Synthesis of 3( [formula omitted])-phosphonoacetyl-2( [formula omitted])-piperidinecarboxylic acid, a conformationally-restricted glutamate antagonist

Synthesis and biological activity of sulfoximine-modified myristic acid analogues

Syntheses of [formula omitted]-2-fluoromethy- [formula omitted]-tyrosine and [formula omitted]-2-difluoromethyl- [formula omitted]-tyrosine as potential inhibitors of tyrosine hydroxylase

Superagonist, Full Agonist, Partial Agonist, and Antagonist Actions of Arylguanidines at 5‑Hydroxytryptamine‑3 (5-HT3) Subunit A Receptors

“Methylene Bridge” to 5‑HT3 Receptor Antagonists: Conformationally Constrained Phenylguanidines

"Methylene Bridge" to 5-HT 3 Receptor Antagonists: Conformationally Constrained Phenylguanidines

Theorizing the Americanist tradition

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