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Total synthesis of (.+-.)-methyl shikimate and (.+-.)-3-phosphoshikimic acid

Journal of the American Chemical Society, 1984-12, Vol.106 (25), p.7854-7860

1984

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Nonsteroidal inhibitors of human type I steroid 5-.alpha.-reductase

Journal of medicinal chemistry, 1993-02, Vol.36 (3), p.421-423

1993

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3-Phenyl-4-hydroxyquinolin-2(1H)-ones: potent and selective antagonists at the strychnine-insensitive glycine site on the N-methyl-D-aspartate receptor complex

Journal of medicinal chemistry, 1992-09, Vol.35 (18), p.3423-3425

1992

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Synthesis and excitatory amino acid pharmacology of a series of heterocyclic-fused quinoxalinones and quinazolinones

Journal of medicinal chemistry, 1992-09, Vol.35 (18), p.3319-3324

1992

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5,7-Dichlorokynurenic acid, a potent and selective competitive antagonist of the glycine site on NMDA receptors

Neuroscience letters, 1990-11, Vol.120 (1), p.17-20

1990

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An enantioselective synthesis of D-(-)- and L-(+)-2-amino-3-phosphonopropanoic acid

Journal of organic chemistry, 1990-07, Vol.55 (14), p.4472-4474

1990

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Substituted 5-amino-4,5,6,7-tetrahydroindazoles as partial ergoline structures with dopaminergic activity

Journal of medicinal chemistry, 1989-10, Vol.32 (10), p.2388-2396

1989

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Stereoselectivity and mode of inhibition of phosphoinositide-coupled excitatory amino acid receptors by 2-amino-3-phosphonopropionic acid

Molecular pharmacology, 1990-08, Vol.38 (2), p.222-228

1990

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Synthesis and 5α-reductase inhibitory activity of 8-substituted benzo[ƒ]quinolinones derived from palladium mediated coupling reactions

Bioorganic & medicinal chemistry letters, 1998-02, Vol.8 (4), p.395-398

1998

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Structure-activity relationships of a series of glycine antagonists related to 5,7-dichlorokynurenic acid and 3-(2-carboxy-6-chloroindol-3-yl)acetic acid

Bioorganic & medicinal chemistry letters, 1993, Vol.3 (1), p.81-84

1993

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QSAR study of benzoquinolinones as inhibitors of human type 1 5-α-reductase

Bioorganic & medicinal chemistry letters, 1993-06, Vol.3 (6), p.1157-1162

1993

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LY191704: A Selective, Nonsteroidal Inhibitor of Human Steroid 5α- Reductase Type 1

Proceedings of the National Academy of Sciences - PNAS, 1993-06, Vol.90 (11), p.5277-5281

1993

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LY191704 inhibits type I steroid 5α-reductase in human scalp

The journal of clinical endocrinology and metabolism, 1996-06, Vol.81 (6), p.2055-2060

1996

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Creation of a Knowledge-Based System to Accelerate Drug Development

Drug information journal, 1999, Vol.33 (2), p.641-648

1999

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SYNTHESIS OF SHIKIMIC ACID AND 3-PHOSPHOSHIKIMIC ACID

MCQUAID, LORETTA AMES

1983

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Total synthesis of (.+-.)-methyl shikimate and (.+-.)-3-phosphoshikimic acid

Nonsteroidal inhibitors of human type I steroid 5-.alpha.-reductase

3-Phenyl-4-hydroxyquinolin-2(1H)-ones: potent and selective antagonists at the strychnine-insensitive glycine site on the N-methyl-D-aspartate receptor complex

Synthesis and excitatory amino acid pharmacology of a series of heterocyclic-fused quinoxalinones and quinazolinones

5,7-Dichlorokynurenic acid, a potent and selective competitive antagonist of the glycine site on NMDA receptors

An enantioselective synthesis of D-(-)- and L-(+)-2-amino-3-phosphonopropanoic acid

Substituted 5-amino-4,5,6,7-tetrahydroindazoles as partial ergoline structures with dopaminergic activity

Stereoselectivity and mode of inhibition of phosphoinositide-coupled excitatory amino acid receptors by 2-amino-3-phosphonopropionic acid

Synthesis and 5α-reductase inhibitory activity of 8-substituted benzo[ƒ]quinolinones derived from palladium mediated coupling reactions

Structure-activity relationships of a series of glycine antagonists related to 5,7-dichlorokynurenic acid and 3-(2-carboxy-6-chloroindol-3-yl)acetic acid

QSAR study of benzoquinolinones as inhibitors of human type 1 5-α-reductase

LY191704: A Selective, Nonsteroidal Inhibitor of Human Steroid 5α- Reductase Type 1

LY191704 inhibits type I steroid 5α-reductase in human scalp

Creation of a Knowledge-Based System to Accelerate Drug Development

SYNTHESIS OF SHIKIMIC ACID AND 3-PHOSPHOSHIKIMIC ACID

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