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To automate or not to automate: this is the question

Journal of structural and functional genomics, 2010-09, Vol.11 (3), p.211-221

2010

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Novel AMPA receptor potentiators LY392098 and LY404187: effects on recombinant human AMPA receptors in vitro

Neuropharmacology, 2001-06, Vol.40 (8), p.976-983

2001

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Identification of the First trans-(3R,4R)- Dimethyl-4-(3-hydroxyphenyl)piperidine Derivative To Possess Highly Potent and Selective Opioid κ Receptor Antagonist Activity

Journal of medicinal chemistry, 2001-08, Vol.44 (17), p.2687-2690

2001

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Synthesis and Evaluation of a Series of Novel 2-[(4-Chlorophenoxy)methyl]- benzimidazoles as Selective Neuropeptide Y Y1 Receptor Antagonists

Journal of medicinal chemistry, 1998-07, Vol.41 (15), p.2709-2719

1998

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The stimulus properties of LSD in C57BL/6 mice

Pharmacology, biochemistry and behavior, 2005-08, Vol.81 (4), p.830-837

2005

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Biarylpropylsulfonamides as Novel, Potent Potentiators of 2-Amino-3- (5-methyl-3-hydroxyisoxazol-4-yl)- propanoic Acid (AMPA) Receptors

Journal of medicinal chemistry, 2000-11, Vol.43 (23), p.4354-4358

2000

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Structure-activity relationship of a series of diaminoalkyl substituted benzimidazole as neuropeptide Y Y1 receptor antagonists

Bioorganic & medicinal chemistry letters, 1999-03, Vol.9 (5), p.647-652

1999

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Enteric (Typhoid) Fever in Travelers

Clinical infectious diseases, 2005-11, Vol.41 (10), p.1467-1472

2005

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Potent and Selective 1,2,3-Trisubstituted Indole NPY Y-1 Antagonists

Journal of medicinal chemistry, 1997-11, Vol.40 (23), p.3712-3714

1997

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In vivo myocardial protection from ischemia/reperfusion injury by the peroxisome proliferator-activated receptor-γ agonist rosiglitazone

Circulation (New York, N.Y.), 2001-11, Vol.104 (21), p.2588-2594

2001

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Selective opioid receptor agonists and antagonists: research tools and potential therapeutic agents

Journal of medicinal chemistry, 1990-03, Vol.33 (3), p.895-902

1990

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Identification of an Opioid κ Receptor Subtype-Selective N-Substituent for (+)-(3R,4R)-Dimethyl-4-(3-hydroxyphenyl)piperidine

Journal of medicinal chemistry, 1998-12, Vol.41 (26), p.5188-5197

1998

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Use of beta-funaltrexamine to determine mu opioid receptor involvement in the analgesic activity of various opioid ligands

The Journal of pharmacology and experimental therapeutics, 1987-05, Vol.241 (2), p.374

1987

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Crystal structure of 6-(4-difluoromethoxy-3-methoxyphenyl)-3(2H)- pyridazinone, C12H10F2N2O3

Zeitschrift für Kristallographie. New crystal structures, 2006-09, Vol.221 (3), p.359-360

2006

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Investigation of the N-Substituent Conformation Governing Potency and μ Receptor Subtype-Selectivity in (+)-(3R,4R)-Dimethyl-4-(3-hydroxyphenyl)- piperidine Opioid Antagonists

Journal of medicinal chemistry, 1998-05, Vol.41 (11), p.1980-1990

1998

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Clinical Features of Scrub Typhus

Clinical infectious diseases, 2006-05, Vol.42 (10), p.1505-1506

2006

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Molecular structure and pharmacological characterization of humEAA2, a novel human kainate receptor subunit

Molecular pharmacology, 1992-07, Vol.42 (1), p.10-15

1992

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Anticonvulsant effects of phencyclidine-like drugs: relation to N-methyl- d-aspartic acid antagonism

Brain research, 1988-06, Vol.454 (1), p.368-372

1988

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Synthesis of a Series of Aryl Kainic Acid Analogs and Evaluation in Cells Stably Expressing the Kainate Receptor humGluR6

Journal of medicinal chemistry, 1996-09, Vol.39 (19), p.3617-3624

1996

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N-methyl-D-aspartic acid-induced lethality in mice: selective antagonism by phencyclidine-like drugs

Brain research, 1988-05, Vol.448 (1), p.115-120

1988

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Experimental and ab initio studies of the gas-phase basicities of polyglycines

Journal of the American Chemical Society, 1993-11, Vol.115 (23), p.10812-10822

1993

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What is an Intensive Care Unit (ICU): A Report of the Task Force of the World Federation of Societies of Intensive and Critical Care Medicine

Journal of critical care, 2017-02, Vol.37, p.270-276

2017

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Structure-activity relationships of a series of benzothiophene-derived NPY Y1 antagonists: Optimization of the C-2 side chain

Bioorganic & medicinal chemistry letters, 1999-02, Vol.9 (3), p.475-480

1999

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Molecular Cloning, Expression, and Pharmacological Characterization of humEAA1, a Human Kainate Receptor Subunit

Journal of neurochemistry, 1994-01, Vol.62 (1), p.1-9

1994

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To automate or not to automate: this is the question

Novel AMPA receptor potentiators LY392098 and LY404187: effects on recombinant human AMPA receptors in vitro

Identification of the First trans-(3R,4R)- Dimethyl-4-(3-hydroxyphenyl)piperidine Derivative To Possess Highly Potent and Selective Opioid κ Receptor Antagonist Activity

Synthesis and Evaluation of a Series of Novel 2-[(4-Chlorophenoxy)methyl]- benzimidazoles as Selective Neuropeptide Y Y1 Receptor Antagonists

The stimulus properties of LSD in C57BL/6 mice

Biarylpropylsulfonamides as Novel, Potent Potentiators of 2-Amino-3- (5-methyl-3-hydroxyisoxazol-4-yl)- propanoic Acid (AMPA) Receptors

Structure-activity relationship of a series of diaminoalkyl substituted benzimidazole as neuropeptide Y Y1 receptor antagonists

Enteric (Typhoid) Fever in Travelers

Potent and Selective 1,2,3-Trisubstituted Indole NPY Y-1 Antagonists

In vivo myocardial protection from ischemia/reperfusion injury by the peroxisome proliferator-activated receptor-γ agonist rosiglitazone

Selective opioid receptor agonists and antagonists: research tools and potential therapeutic agents

Identification of an Opioid κ Receptor Subtype-Selective N-Substituent for (+)-(3R,4R)-Dimethyl-4-(3-hydroxyphenyl)piperidine

Use of beta-funaltrexamine to determine mu opioid receptor involvement in the analgesic activity of various opioid ligands

Crystal structure of 6-(4-difluoromethoxy-3-methoxyphenyl)-3(2H)- pyridazinone, C12H10F2N2O3

Investigation of the N-Substituent Conformation Governing Potency and μ Receptor Subtype-Selectivity in (+)-(3R,4R)-Dimethyl-4-(3-hydroxyphenyl)- piperidine Opioid Antagonists

Clinical Features of Scrub Typhus

Diffuse interstitial fibrosis assessed by cardiac magnetic resonance is associated with dispersion of ventricular repolarization in patients with hypertrophic cardiomyopathy

Molecular structure and pharmacological characterization of humEAA2, a novel human kainate receptor subunit

Anticonvulsant effects of phencyclidine-like drugs: relation to N-methyl- d-aspartic acid antagonism

Synthesis of a Series of Aryl Kainic Acid Analogs and Evaluation in Cells Stably Expressing the Kainate Receptor humGluR6

N-methyl-D-aspartic acid-induced lethality in mice: selective antagonism by phencyclidine-like drugs

Experimental and ab initio studies of the gas-phase basicities of polyglycines

What is an Intensive Care Unit (ICU): A Report of the Task Force of the World Federation of Societies of Intensive and Critical Care Medicine

Structure-activity relationships of a series of benzothiophene-derived NPY Y1 antagonists: Optimization of the C-2 side chain

Molecular Cloning, Expression, and Pharmacological Characterization of humEAA1, a Human Kainate Receptor Subunit

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