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Biochemical and behavioural characterization of EMPA, a novel high‐affinity, selective antagonist for the OX2 receptor

British journal of pharmacology, 2009-04, Vol.156 (8), p.1326-1341

2009

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Biochemical and behavioural characterization of EMPA, a novel high‐affinity, selective antagonist for the OX 2 receptor

British journal of pharmacology, 2009-04, Vol.156 (8), p.1326-1341

2009

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Combinatorial Synthesis of 5-Aryl-[1,2,4]-triazolo-[1,5-a]-pyridine Derivatives as Potential Inhibitors of the Adenosine 2A Receptor

Synlett, 2001, Vol.2001 (12), p.1917-1920

Nettekoven, Matthias

2001

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Discovery of potent and selective histamine H3 receptor inverse agonists based on the 3,4-dihydro-2H-pyrazino[1,2-a]indol-1-one scaffold

Bioorganic & medicinal chemistry letters, 2010-10, Vol.20 (19), p.5713-5717

2010

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A combinatorial approach towards 2-acyl-3-amino-indole derivatives

Tetrahedron letters, 2000-10, Vol.41 (43), p.8251-8254

Nettekoven, Matthias

2000

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Combinatorial synthesis of libraries of indole derivatives

Bioorganic & medicinal chemistry letters, 2001-08, Vol.11 (16), p.2169-2171

Nettekoven, Matthias

2001

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Novel and potent NPY5 receptor antagonists derived from virtual screening and iterative parallel chemistry design

Bioorganic & medicinal chemistry letters, 2005-03, Vol.15 (6), p.1599-1603

2005

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Lead generation--enhancing the success of drug discovery by investing in the hit to lead process

Combinatorial chemistry & high throughput screening, 2003-02, Vol.6 (1), p.51-66

2003

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Comparison of inhibitory activity of isomeric triazolopyridine derivatives towards adenosine receptor subtypes or do similar structures reveal similar bioactivities?

Bioorganic & medicinal chemistry letters, 2004-06, Vol.14 (12), p.3307-3312

2004

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The Development of a Practical and Reliable Large-Scale Synthesis of 2,6-Diamino-4-bromopyridine

Organic process research & development, 2003-01, Vol.7 (1), p.38-43

2003

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Discovery of potent and selective histamine H 3 receptor inverse agonists based on the 3,4-dihydro-2 H-pyrazino[1,2- a]indol-1-one scaffold

Bioorganic & medicinal chemistry letters, 2010, Vol.20 (19), p.5713-5717

2010

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Accelerating drug discovery by integrative implementation of laboratory automation in the work flow

Current medicinal chemistry, 2002-12, Vol.9 (23), p.2179-2190

2002

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Synthetic Access to 2-Amido-5-aryl-8-methoxy-triazolopyridine and 2-Amido-5-morpholino-8-methoxy-triazolopyridine Derivatives as Potential Inhibitors of the Adenosine Receptor Subtypes

Synthesis (Stuttgart), 2003-01, Vol.2003 (11)

2003

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The phytopathogenic fungus Cladosporium fulvum is not sensitive to the chitinase and β-1,3-glucanase defence proteins of its host, tomato

Physiological and molecular plant pathology, 1995, Vol.46 (1), p.45-59

1995

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Isomeric thiazole derivatives as ligands for the neuropeptide Y5 receptor

Bioorganic & medicinal chemistry letters, 2005-07, Vol.15 (14), p.3446-3449

2005

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Parallel iterative solution-phase synthesis of 5-amino-1-aryl-[1,2,4]triazolo[1,5- a]pyridine-7-carboxylic acid amide derivatives

Tetrahedron letters, 2003-02, Vol.44 (8), p.1675-1678

2003

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Lead Generation: Sowing the Seeds for Future Success

Chimia, 2004-09, Vol.58 (9), p.588

2004

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NTMS Facial Mapping: Mental Muscle superior to Orbicularis Oris Muscle: A Technical Note

Klinische Neurophysiologie, 2012-03, Vol.43 (1)

2012

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NEW POLYETHYLENE GLYCOL POLYMERS AS KETAL PROTECTING GROUPS - A POLYMER SUPPORTED APPROACH TO SYMMETRICALLY SUBSTITUTED SPIROKETALS

Synthetic communications, 2001-01, Vol.31 (19), p.2965-2977

2001

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Biochemical and behavioural characterization of EMPA, a novel high-affinity, selective antagonist for the OX(2) receptor

British journal of pharmacology, 2009-04, Vol.156 (8), p.1326

2009

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Synthesis of enantiomerically pure 4-alkylsubstituted tryptophan derivatives by a combination of organometallic reactions with enantioselective enzymatic transformations

Tetrahedron letters, 1995, Vol.36 (9), p.1428-1428

1995

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A panel data analysis: research and development spillover

Economics letters, 1999-07, Vol.64 (1), p.37-41

1999

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Ligand-Based Combinatorial Design of Selective Purinergic Receptor (A2A) Antagonists Using Self-Organizing Maps

Journal of combinatorial chemistry, 2003-05, Vol.5 (3), p.233-237

2003

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Test-retest reliability of primary motor cortex mapping: Neuronavigated transcranial magnetic brain stimulation versus functional MRI

Klinische Neurophysiologie, 2012, Vol.43 (1)

2012

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The importance of latency correction for navigated TMS mapping, especially of the face and tongue area: A Technical Note

Klinische Neurophysiologie, 2012, Vol.43 (1)

2012

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Biochemical and behavioural characterization of EMPA, a novel high‐affinity, selective antagonist for the OX2 receptor

Biochemical and behavioural characterization of EMPA, a novel high‐affinity, selective antagonist for the OX 2 receptor

Combinatorial Synthesis of 5-Aryl-[1,2,4]-triazolo-[1,5-a]-pyridine Derivatives as Potential Inhibitors of the Adenosine 2A Receptor

Discovery of potent and selective histamine H3 receptor inverse agonists based on the 3,4-dihydro-2H-pyrazino[1,2-a]indol-1-one scaffold

A combinatorial approach towards 2-acyl-3-amino-indole derivatives

Combinatorial synthesis of libraries of indole derivatives

Novel and potent NPY5 receptor antagonists derived from virtual screening and iterative parallel chemistry design

Lead generation--enhancing the success of drug discovery by investing in the hit to lead process

Comparison of inhibitory activity of isomeric triazolopyridine derivatives towards adenosine receptor subtypes or do similar structures reveal similar bioactivities?

The Development of a Practical and Reliable Large-Scale Synthesis of 2,6-Diamino-4-bromopyridine

Discovery of potent and selective histamine H 3 receptor inverse agonists based on the 3,4-dihydro-2 H-pyrazino[1,2- a]indol-1-one scaffold

Accelerating drug discovery by integrative implementation of laboratory automation in the work flow

Synthetic Access to 2-Amido-5-aryl-8-methoxy-triazolopyridine and 2-Amido-5-morpholino-8-methoxy-triazolopyridine Derivatives as Potential Inhibitors of the Adenosine Receptor Subtypes

The phytopathogenic fungus Cladosporium fulvum is not sensitive to the chitinase and β-1,3-glucanase defence proteins of its host, tomato

Isomeric thiazole derivatives as ligands for the neuropeptide Y5 receptor

Parallel iterative solution-phase synthesis of 5-amino-1-aryl-[1,2,4]triazolo[1,5- a]pyridine-7-carboxylic acid amide derivatives

Lead Generation: Sowing the Seeds for Future Success

NTMS Facial Mapping: Mental Muscle superior to Orbicularis Oris Muscle: A Technical Note

NEW POLYETHYLENE GLYCOL POLYMERS AS KETAL PROTECTING GROUPS - A POLYMER SUPPORTED APPROACH TO SYMMETRICALLY SUBSTITUTED SPIROKETALS

Biochemical and behavioural characterization of EMPA, a novel high-affinity, selective antagonist for the OX(2) receptor

Synthesis of enantiomerically pure 4-alkylsubstituted tryptophan derivatives by a combination of organometallic reactions with enantioselective enzymatic transformations

A panel data analysis: research and development spillover

Ligand-Based Combinatorial Design of Selective Purinergic Receptor (A2A) Antagonists Using Self-Organizing Maps

Test-retest reliability of primary motor cortex mapping: Neuronavigated transcranial magnetic brain stimulation versus functional MRI

The importance of latency correction for navigated TMS mapping, especially of the face and tongue area: A Technical Note

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