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Functional connection between posterior superior temporal gyrus and ventrolateral prefrontal cortex in human

Cerebral cortex (New York, N.Y. 1991), 2013-10, Vol.23 (10), p.2309-2321

2013

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Nonpeptide Angiotensin II Receptor Antagonists: The Next Generation in Antihypertensive Therapy

Journal of medicinal chemistry, 1996-02, Vol.39 (3), p.625-656

1996

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High-gamma band fronto-temporal coherence as a measure of functional connectivity in speech motor control

Neuroscience, 2015-10, Vol.305, p.15-25

2015

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Discovery of Potent Orally Active Thrombin Receptor (Protease Activated Receptor 1) Antagonists as Novel Antithrombotic Agents

Journal of medicinal chemistry, 2005-09, Vol.48 (19), p.5884-5887

2005

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Tetrahydroisoquinolines as MCH-R1 antagonists

Bioorganic & medicinal chemistry letters, 2006-09, Vol.16 (18), p.4917-4921

2006

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SCH-C (SCH 351125), An Orally Bioavailable, Small Molecule Antagonist of the Chemokine Receptor CCR5, is a Potent Inhibitor of HIV-1 Infection in vitro and in vivo

Proceedings of the National Academy of Sciences - PNAS, 2001-10, Vol.98 (22), p.12718-12723

2001

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Discovery of 4-[(Z)-(4-Bromophenyl)- (ethoxyimino)methyl]-1‘-[(2,4-dimethyl-3- pyridinyl)carbonyl]-4‘-methyl-1,4‘- bipiperidine N-Oxide (SCH 351125): An Orally Bioavailable Human CCR5 Antagonist for the Treatment of HIV Infection

Journal of medicinal chemistry, 2001-10, Vol.44 (21), p.3339-3342

2001

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Discovery of Orally Efficacious Melanin-Concentrating Hormone Receptor-1 Antagonists as Antiobesity Agents. Synthesis, SAR, and Biological Evaluation of Bicyclo[3.1.0]hexyl Ureas

Journal of medicinal chemistry, 2006-04, Vol.49 (7), p.2294-2310

2006

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Discovery of Bicycloalkyl Urea Melanin Concentrating Hormone Receptor Antagonists: Orally Efficacious Antiobesity Therapeutics

Journal of medicinal chemistry, 2005-04, Vol.48 (7), p.2274-2277

2005

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In vitro pharmacology of L-158,809, a new highly potent and selective angiotensin II receptor antagonist

The Journal of pharmacology and experimental therapeutics, 1992-07, Vol.262 (1), p.133

1992

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In vivo pharmacology of L-158,809, a new highly potent and selective nonpeptide angiotensin II receptor antagonist

The Journal of pharmacology and experimental therapeutics, 1992-07, Vol.262 (1), p.139

1992

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Synthesis, SAR, and Biological Evaluation of Oximino-Piperidino-Piperidine Amides. 1. Orally Bioavailable CCR5 Receptor Antagonists with Potent Anti-HIV Activity

Journal of medicinal chemistry, 2002-07, Vol.45 (14), p.3143-3160

2002

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Discovery of L-162,313: a nonpeptide that mimics the biological actions of angiotensin II

American journal of physiology. Regulatory, integrative and comparative physiology, 1995-03, Vol.268 (3), p.820-R823

1995

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Identification of peptide binding residues in the extracellular domains of the AT1 receptor

The Journal of biological chemistry, 1994-12, Vol.269 (49), p.30953-30959

1994

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Renin inhibitors

Pharmaceutical research, 1987-10, Vol.4 (5), p.364-374

GREENLEE, W. J

1987

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Effects of subtype-selective and balanced angiotensin II receptor antagonists in a porcine coronary artery model of vascular restenosis

Circulation (New York, N.Y.), 1996-03, Vol.93 (5), p.1009-1019

1996

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A new class of angiotensin-converting enzyme inhibitors

Nature (London), 1980-11, Vol.288 (5788), p.280-283

1980

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Nonpeptide angiotensin II antagonists derived from 1H-pyrazole-5-carboxylates and 4-aryl-1H-imidazole-5-carboxylates

Journal of medicinal chemistry, 1993-11, Vol.36 (23), p.3595-3605

1993

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5-Chloro-3-(phenylsulfonyl)indole-2-carboxamide: a novel, non-nucleoside inhibitor of HIV-1 reverse transcriptase

Journal of medicinal chemistry, 1993-04, Vol.36 (9), p.1291-1294

1993

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Renal protection by a dual ETA/ETB endothelin antagonist, L-754,142, after aortic cross-clamping in the dog

Journal of the American Society of Nephrology, 1997-07, Vol.8 (7), p.1061-1071

1997

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Design of a selective insulin receptor tyrosine kinase inhibitor and its effect on glucose uptake and metabolism in intact cells

Biochemistry (Easton), 1989-06, Vol.28 (13), p.5694-5701

1989

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Synthesis of .beta.,.gamma.-unsaturated amino acids by the Strecker reaction

Journal of organic chemistry, 1984-07, Vol.49 (14), p.2632-2634

Greenlee, W. J

1984

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(3-Amino-2-oxoalkyl)phosphonic acids and their analogs as novel inhibitors of D-alanine:D-alanine ligase

Journal of medicinal chemistry, 1989-08, Vol.32 (8), p.1886-1890

1989

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A nonpeptidic agonist ligand of the human C5a receptor: Synthesis, binding affinity optimization and functional characterization

Bioorganic & medicinal chemistry letters, 1997-01, Vol.7 (2), p.213-218

1997

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Design and synthesis of P2-P1'-linked macrocyclic human renin inhibitors

Journal of medicinal chemistry, 1991-09, Vol.34 (9), p.2692-2701

1991

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Functional connection between posterior superior temporal gyrus and ventrolateral prefrontal cortex in human

Nonpeptide Angiotensin II Receptor Antagonists: The Next Generation in Antihypertensive Therapy

High-gamma band fronto-temporal coherence as a measure of functional connectivity in speech motor control

Discovery of Potent Orally Active Thrombin Receptor (Protease Activated Receptor 1) Antagonists as Novel Antithrombotic Agents

Tetrahydroisoquinolines as MCH-R1 antagonists

SCH-C (SCH 351125), An Orally Bioavailable, Small Molecule Antagonist of the Chemokine Receptor CCR5, is a Potent Inhibitor of HIV-1 Infection in vitro and in vivo

Discovery of 4-[(Z)-(4-Bromophenyl)- (ethoxyimino)methyl]-1‘-[(2,4-dimethyl-3- pyridinyl)carbonyl]-4‘-methyl-1,4‘- bipiperidine N-Oxide (SCH 351125): An Orally Bioavailable Human CCR5 Antagonist for the Treatment of HIV Infection

Discovery of Orally Efficacious Melanin-Concentrating Hormone Receptor-1 Antagonists as Antiobesity Agents. Synthesis, SAR, and Biological Evaluation of Bicyclo[3.1.0]hexyl Ureas

Discovery of Bicycloalkyl Urea Melanin Concentrating Hormone Receptor Antagonists: Orally Efficacious Antiobesity Therapeutics

In vitro pharmacology of L-158,809, a new highly potent and selective angiotensin II receptor antagonist

In vivo pharmacology of L-158,809, a new highly potent and selective nonpeptide angiotensin II receptor antagonist

Synthesis, SAR, and Biological Evaluation of Oximino-Piperidino-Piperidine Amides. 1. Orally Bioavailable CCR5 Receptor Antagonists with Potent Anti-HIV Activity

Discovery of L-162,313: a nonpeptide that mimics the biological actions of angiotensin II

Identification of peptide binding residues in the extracellular domains of the AT1 receptor

Renin inhibitors

Effects of subtype-selective and balanced angiotensin II receptor antagonists in a porcine coronary artery model of vascular restenosis

A new class of angiotensin-converting enzyme inhibitors

Nonpeptide angiotensin II antagonists derived from 1H-pyrazole-5-carboxylates and 4-aryl-1H-imidazole-5-carboxylates

5-Chloro-3-(phenylsulfonyl)indole-2-carboxamide: a novel, non-nucleoside inhibitor of HIV-1 reverse transcriptase

Renal protection by a dual ETA/ETB endothelin antagonist, L-754,142, after aortic cross-clamping in the dog

Design of a selective insulin receptor tyrosine kinase inhibitor and its effect on glucose uptake and metabolism in intact cells

Synthesis of .beta.,.gamma.-unsaturated amino acids by the Strecker reaction

(3-Amino-2-oxoalkyl)phosphonic acids and their analogs as novel inhibitors of D-alanine:D-alanine ligase

A nonpeptidic agonist ligand of the human C5a receptor: Synthesis, binding affinity optimization and functional characterization

Design and synthesis of P2-P1'-linked macrocyclic human renin inhibitors

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