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Determination of physiological, taxonomic, and molecular characteristics of a cultivable arsenic-resistant bacterial community

Environmental science and pollution research international, 2015-09, Vol.22 (18), p.13753-13763

2015

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Synthesis of enantiomerically pure ethylenediamines from chiral sulfinimines: a new twist to the Strecker reaction

Tetrahedron, 2001-10, Vol.57 (42), p.8861-8866

2001

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Structure−Activity Relationships in a Series of 2(1H)-Quinolones Bearing Different Acidic Function in the 3-Position: 6,7-Dichloro-2(1H)-oxoquinoline-3-phosphonic Acid, a New Potent and Selective AMPA/Kainate Antagonist with Neuroprotective Properties

Journal of medicinal chemistry, 1996-01, Vol.39 (1), p.197-206

1996

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Potential Antidepressants Displayed Combined α2-Adrenoceptor Antagonist and Monoamine Uptake Inhibitor Properties

Journal of medicinal chemistry, 2001-03, Vol.44 (5), p.787-805

2001

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D-cycloserine, a positive modulator of the N-methyl-D-aspartate receptor, enhances performance of learning tasks in rats

Pharmacology, biochemistry and behavior, 1989-11, Vol.34 (3), p.649-653

1989

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Novel RGD-like molecules based on the tyrosine template design, synthesis, and biological evaluation on isolated integrins alpha(V)beta/alpha(IIb)beta(3) and in cellular adhesion tests

2004-10

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αvβ3 Integrin-Targeting Arg-Gly-Asp (RGD) Peptidomimetics Containing Oligoethylene Glycol (OEG) Spacers

Journal of medicinal chemistry, 2009-11, Vol.52 (22), p.7029-7043

2009

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Unsuspected Diversity of Arsenite-Oxidizing Bacteria as Revealed by Widespread Distribution of the aoxB Gene in Prokaryotes

Applied and Environmental Microbiology, 2011-07, Vol.77 (13), p.4685-4692

2011

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Inhibition of amine oxidase activity by derivatives that recognize imidazoline I2 sites

The Journal of pharmacology and experimental therapeutics, 1995-02, Vol.272 (2), p.681

1995

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In vivo analysis of adrenergic and serotoninergic constrictions of the rabbit saphenous vein

European journal of pharmacology, 2000-11, Vol.408 (3), p.277-288

2000

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Role of thromboxane TP and angiotensin AT1 receptors in lipopolysaccharide-induced arterial dysfunction in the rabbit: an in vivo study

European journal of pharmacology, 2010-05, Vol.634 (1-3), p.113-120

2010

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Assessment of Anti-Migraine Potential of a Novel α-Adrenoceptor Agonist S19014: Effects on Porcine Carotid and Regional Haemodynamics and Human Coronary Artery

Cephalalgia, 2004-06, Vol.24 (6), p.425-438

2004

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Design, synthesis and structure-activity relationships of novel strychnine-insensitive glycine receptor ligands

Bioorganic & medicinal chemistry letters, 1999-05, Vol.9 (10), p.1409-1414

1999

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Enantioselective synthesis of a pyrrolo-benzothiadiazine derivative S 18986, a new AMPA receptor positive modulator

Bioorganic & medicinal chemistry letters, 1996-12, Vol.6 (24), p.3003-3008

1996

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Potential antidepressants displayed combined alpha(2)-adrenoceptor antagonist and monoamine uptake inhibitor properties

Journal of medicinal chemistry, 2001-03, Vol.44 (5), p.787-805

2001

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Synthesis and biological evaluation of cyclopropyl analogs of 2-amino-5-phosphonopentanoic acid

Journal of medicinal chemistry, 1991-01, Vol.34 (1), p.161-168

1991

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Novel indole-2-carboxylates as ligands for the strychnine-insensitive N-methyl-D-aspartate-linked glycine receptor

Journal of medicinal chemistry, 1991-04, Vol.34 (4), p.1283-1292

1991

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Design, synthesis, and structure-activity Relationships of a new series of .alpha.-adrenergic agonists: spiro[(1,3-diazacycylpent-1-ent)-5,2'-(1',2',3',4'-tetrahydronaphthalene)]

Journal of medicinal chemistry, 1995-09, Vol.38 (20), p.4056-4069

1995

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Recording of the saphenous vein compliance by an ultrasonic echo‐tracking device in the dog: effects of S 18149

British journal of pharmacology, 1997-12, Vol.122 (7), p.1361-1366

1997

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[3H]‐idazoxan binding to rabbit cerebral cortex recognises multiple imidazoline I2‐type receptors: pharmacological characterization and relationship to monoamine oxidase

British journal of pharmacology, 1993-07, Vol.109 (3), p.625-631

1993

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Milacemide, a glycine prodrug, enhances performance of learning tasks in normal and amnestic rodents

Pharmacology, biochemistry and behavior, 1989-12, Vol.34 (4), p.823-828

1989

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S28 NMDA RECEPTORS AND COGNITION: THE GLYCINE B CO-AGONIST SITE AS A TARGET FOR IMPROVING COGNITIVE PERFORMANCE IN SCHIZOPHRENIA?

Behavioural pharmacology, 2005-09, Vol.16 (Supplement 1), p.S9

2005

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Structure-activity relationships in a series of 3-sulfonylamino-2-(1 H)-quinolones, as new AMPA/Kainate and glycine antagonists

Bioorganic & medicinal chemistry, 1995-02, Vol.3 (2), p.129-141

1995

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The synthesis of novel melphalan derivatives as potential antineoplastic agents

European journal of medicinal chemistry, 1997, Vol.32 (4), p.343-349

1997

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A comparative study of the reversal by different α2‐adrenoceptor antagonists of the central sympatho‐inhibitory effect of clonidine

British journal of pharmacology, 1996-02, Vol.117 (3), p.587-593

1996

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Determination of physiological, taxonomic, and molecular characteristics of a cultivable arsenic-resistant bacterial community

Synthesis of enantiomerically pure ethylenediamines from chiral sulfinimines: a new twist to the Strecker reaction

Structure−Activity Relationships in a Series of 2(1H)-Quinolones Bearing Different Acidic Function in the 3-Position: 6,7-Dichloro-2(1H)-oxoquinoline-3-phosphonic Acid, a New Potent and Selective AMPA/Kainate Antagonist with Neuroprotective Properties

Potential Antidepressants Displayed Combined α2-Adrenoceptor Antagonist and Monoamine Uptake Inhibitor Properties

D-cycloserine, a positive modulator of the N-methyl-D-aspartate receptor, enhances performance of learning tasks in rats

Novel RGD-like molecules based on the tyrosine template design, synthesis, and biological evaluation on isolated integrins alpha(V)beta/alpha(IIb)beta(3) and in cellular adhesion tests

αvβ3 Integrin-Targeting Arg-Gly-Asp (RGD) Peptidomimetics Containing Oligoethylene Glycol (OEG) Spacers

Unsuspected Diversity of Arsenite-Oxidizing Bacteria as Revealed by Widespread Distribution of the aoxB Gene in Prokaryotes

Inhibition of amine oxidase activity by derivatives that recognize imidazoline I2 sites

In vivo analysis of adrenergic and serotoninergic constrictions of the rabbit saphenous vein

Role of thromboxane TP and angiotensin AT1 receptors in lipopolysaccharide-induced arterial dysfunction in the rabbit: an in vivo study

Assessment of Anti-Migraine Potential of a Novel α-Adrenoceptor Agonist S19014: Effects on Porcine Carotid and Regional Haemodynamics and Human Coronary Artery

Design, synthesis and structure-activity relationships of novel strychnine-insensitive glycine receptor ligands

Enantioselective synthesis of a pyrrolo-benzothiadiazine derivative S 18986, a new AMPA receptor positive modulator

Potential antidepressants displayed combined alpha(2)-adrenoceptor antagonist and monoamine uptake inhibitor properties

Synthesis and biological evaluation of cyclopropyl analogs of 2-amino-5-phosphonopentanoic acid

Novel indole-2-carboxylates as ligands for the strychnine-insensitive N-methyl-D-aspartate-linked glycine receptor

Design, synthesis, and structure-activity Relationships of a new series of .alpha.-adrenergic agonists: spiro[(1,3-diazacycylpent-1-ent)-5,2'-(1',2',3',4'-tetrahydronaphthalene)]

Recording of the saphenous vein compliance by an ultrasonic echo‐tracking device in the dog: effects of S 18149

[3H]‐idazoxan binding to rabbit cerebral cortex recognises multiple imidazoline I2‐type receptors: pharmacological characterization and relationship to monoamine oxidase

Milacemide, a glycine prodrug, enhances performance of learning tasks in normal and amnestic rodents

S28 NMDA RECEPTORS AND COGNITION: THE GLYCINE B CO-AGONIST SITE AS A TARGET FOR IMPROVING COGNITIVE PERFORMANCE IN SCHIZOPHRENIA?

Structure-activity relationships in a series of 3-sulfonylamino-2-(1 H)-quinolones, as new AMPA/Kainate and glycine antagonists

The synthesis of novel melphalan derivatives as potential antineoplastic agents

A comparative study of the reversal by different α2‐adrenoceptor antagonists of the central sympatho‐inhibitory effect of clonidine

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