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New Inhibitors of Angiogenesis with Antitumor Activity in Vivo

Journal of medicinal chemistry, 2015-05, Vol.58 (9), p.3757-3766

2015

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Structure–Activity Relationship of a New Series of Reversible Dual Monoacylglycerol Lipase/Fatty Acid Amide Hydrolase Inhibitors

Journal of medicinal chemistry, 2012-01, Vol.55 (2), p.824-836

2012

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Inside Cover: A Reversible and Selective Inhibitor of Monoacylglycerol Lipase Ameliorates Multiple Sclerosis (Angew. Chem. Int. Ed. 50/2014)

Angewandte Chemie (International ed.), 2014-12, Vol.53 (50), p.13624-13624

International ed. in English, 2014

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Development of Endocannabinoid-Based Chemical Probes for the Study of Cannabinoid Receptors

Journal of medicinal chemistry, 2011-07, Vol.54 (14), p.5265-5269

2011

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Design, Synthesis and Biological Evaluation of Novel Arachidonic Acid Derivatives as Highly Potent and Selective Endocannabinoid Transporter Inhibitors

Journal of medicinal chemistry, 2001-12, Vol.44 (26), p.4505-4508

2001

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2-Arachidonoylglycerol Reduces Proteoglycans and Enhances Remyelination in a Progressive Model of Demyelination

The Journal of neuroscience, 2017-08, Vol.37 (35), p.8385-8398

2017

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Astroglial monoacylglycerol lipase controls mutant huntingtin-induced damage of striatal neurons

Neuropharmacology, 2019-05, Vol.150, p.134-144

2019

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Development of Non-Peptide Ligands of Growth Factor Receptor-Bound Protein 2-Src Homology 2 Domain Using Molecular Modeling and NMR Spectroscopy

Journal of medicinal chemistry, 2011-02, Vol.54 (4), p.1096-1100

2011

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Development of Molecular Probes for the Human 5-HT6 Receptor

Journal of medicinal chemistry, 2010-10, Vol.53 (19), p.7095-7106

2010

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Development of a Fluorescent Bodipy Probe for Visualization of the Serotonin 5‑HT1A Receptor in Native Cells of the Immune System

Bioconjugate chemistry, 2018-06, Vol.29 (6), p.2021-2027

2018

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A novel inhibitor of fatty acid synthase shows activity against HER2+ breast cancer xenografts and is active in anti-HER2 drug-resistant cell lines

Breast cancer research : BCR, 2011-01, Vol.13 (6), p.R131-R131, Article R131

2011

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Design, synthesis and biological evaluation of new endocannabinoid transporter inhibitors

European journal of medicinal chemistry, 2003-04, Vol.38 (4), p.403-412

2003

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Development of Fluorescent Ligands for the Human 5-HT1A Receptor

ACS medicinal chemistry letters, 2010-09, Vol.1 (6), p.249-253

2010

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A double-blind, randomized, cross-over, placebo-controlled, pilot trial with Sativex in Huntington’s disease

Journal of neurology, 2016-07, Vol.263 (7), p.1390-1400

2016

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Involvement of cannabinoids in cellular proliferation

Mini reviews in medicinal chemistry, 2005-01, Vol.5 (1), p.97-106

2005

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Design, Synthesis, and Biological Evaluation of New Inhibitors of the Endocannabinoid Uptake: Comparison with Effects on Fatty Acid Amidohydrolase

Journal of medicinal chemistry, 2003-04, Vol.46 (8), p.1512-1522

2003

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A Basal Tone of 2-Arachidonoylglycerol Contributes to Early Oligodendrocyte Progenitor Proliferation by Activating Phosphatidylinositol 3-Kinase (PI3K)/AKT and the Mammalian Target of Rapamycin (MTOR) Pathways

Journal of neuroimmune pharmacology, 2015-06, Vol.10 (2), p.309-317

2015

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VR1 receptor modulators as potential drugs for neuropathic pain

Mini reviews in medicinal chemistry, 2003-11, Vol.3 (7), p.729-748

2003

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UCM707, a potent and selective inhibitor of endocannabinoid uptake, potentiates hypokinetic and antinociceptive effects of anandamide

European journal of pharmacology, 2002-08, Vol.449 (1-2), p.99-103

2002

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Dual Inhibition of α/β-Hydrolase Domain 6 and Fatty Acid Amide Hydrolase Increases Endocannabinoid Levels in Neurons

The Journal of biological chemistry, 2011-08, Vol.286 (33), p.28723-28728

2011

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Chemoproteomic Approach to Explore the Target Profile of GPCR ligands: Application to 5-HT sub(1A) and 5-HT sub(6) Receptors

Chemistry : a European journal, 2016-01, Vol.22 (4), p.1313-1321

2016

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Structure−Activity Relationship of a Series of Inhibitors of Monoacylglycerol HydrolysisComparison with Effects upon Fatty Acid Amide Hydrolase

Journal of medicinal chemistry, 2007-10, Vol.50 (20), p.5012-5023

2007

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Innentitelbild: A Reversible and Selective Inhibitor of Monoacylglycerol Lipase Ameliorates Multiple Sclerosis (Angew. Chem. 50/2014)

Angewandte Chemie, 2014-12, Vol.126 (50), p.13842-13842

2014

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New players for the alternative activation of microglia: Beyond Arginase-1

Journal of neuroimmunology, 2014-01, Vol.275 (1), p.164-164

2014

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Neurochemical effects of the endocannabinoid uptake inhibitor UCM707 in various rat brain regions

Life sciences (1973), 2007-02, Vol.80 (10), p.979-988

2007

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New Inhibitors of Angiogenesis with Antitumor Activity in Vivo

Structure–Activity Relationship of a New Series of Reversible Dual Monoacylglycerol Lipase/Fatty Acid Amide Hydrolase Inhibitors

Inside Cover: A Reversible and Selective Inhibitor of Monoacylglycerol Lipase Ameliorates Multiple Sclerosis (Angew. Chem. Int. Ed. 50/2014)

Development of Endocannabinoid-Based Chemical Probes for the Study of Cannabinoid Receptors

Design, Synthesis and Biological Evaluation of Novel Arachidonic Acid Derivatives as Highly Potent and Selective Endocannabinoid Transporter Inhibitors

2-Arachidonoylglycerol Reduces Proteoglycans and Enhances Remyelination in a Progressive Model of Demyelination

Astroglial monoacylglycerol lipase controls mutant huntingtin-induced damage of striatal neurons

Development of Non-Peptide Ligands of Growth Factor Receptor-Bound Protein 2-Src Homology 2 Domain Using Molecular Modeling and NMR Spectroscopy

Development of Molecular Probes for the Human 5-HT6 Receptor

Development of a Fluorescent Bodipy Probe for Visualization of the Serotonin 5‑HT1A Receptor in Native Cells of the Immune System

A novel inhibitor of fatty acid synthase shows activity against HER2+ breast cancer xenografts and is active in anti-HER2 drug-resistant cell lines

Design, synthesis and biological evaluation of new endocannabinoid transporter inhibitors

Development of Fluorescent Ligands for the Human 5-HT1A Receptor

A double-blind, randomized, cross-over, placebo-controlled, pilot trial with Sativex in Huntington’s disease

Involvement of cannabinoids in cellular proliferation

Design, Synthesis, and Biological Evaluation of New Inhibitors of the Endocannabinoid Uptake: Comparison with Effects on Fatty Acid Amidohydrolase

A Basal Tone of 2-Arachidonoylglycerol Contributes to Early Oligodendrocyte Progenitor Proliferation by Activating Phosphatidylinositol 3-Kinase (PI3K)/AKT and the Mammalian Target of Rapamycin (MTOR) Pathways

VR1 receptor modulators as potential drugs for neuropathic pain

UCM707, a potent and selective inhibitor of endocannabinoid uptake, potentiates hypokinetic and antinociceptive effects of anandamide

Dual Inhibition of α/β-Hydrolase Domain 6 and Fatty Acid Amide Hydrolase Increases Endocannabinoid Levels in Neurons

Chemoproteomic Approach to Explore the Target Profile of GPCR ligands: Application to 5-HT sub(1A) and 5-HT sub(6) Receptors

Structure−Activity Relationship of a Series of Inhibitors of Monoacylglycerol HydrolysisComparison with Effects upon Fatty Acid Amide Hydrolase

Innentitelbild: A Reversible and Selective Inhibitor of Monoacylglycerol Lipase Ameliorates Multiple Sclerosis (Angew. Chem. 50/2014)

New players for the alternative activation of microglia: Beyond Arginase-1

Neurochemical effects of the endocannabinoid uptake inhibitor UCM707 in various rat brain regions

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