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Synthesis and Biological Characterization of the New Glycolipid Lactose Undecylenate (URB1418)

Pharmaceuticals (Basel, Switzerland), 2022-04, Vol.15 (4), p.456

2022

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The green screen: Neda and the lost voices

International journal of communication (Online), 2013-07, p.1344

Duranti, Andrea

2013

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Synthesis and Biological Evaluation of 6-IO/I-Sucrose Monoester Glycolipids as Possible New Antifungal Agents

Pharmaceuticals (Basel, Switzerland), 2023-01, Vol.16 (2)

2023

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Gay but not Queer: Defining Liminal Post-queer Identities in Maghrebian Literature

Contemporary French and francophone studies, 2008-01, Vol.12 (1), p.79-87

Duranti, Andrea

2008

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Structural determinants of peripheral O-arylcarbamate FAAH inhibitors render them dual substrates for Abcb1 and Abcg2 and restrict their access to the brain

Pharmacological research, 2014-09, Vol.87, p.87-93

2014

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Erratum to: Increase of brain endocannabinoid anandamide levels by FAAH inhibition and alcohol abuse behaviours in the rat

Psychopharmacology, 2011-07, Vol.216 (1), p.151-151

2011

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Erratum to: increase of brain endocannabinoid anandamide levels by FAAH inhibition and alcohol abuse behaviours in the rat

Psychopharmacology, 2011-07, Vol.216 (1), p.151

2011

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Erratum: The collisional behavior of ESI-generated protonated molecules of some carbamate FAAH inhibitors isosteres and its relationships with biological activity

Journal of mass spectrometry., 2011-08, Vol.46 (8), p.847-847

2011

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Design, synthesis, and pharmacological effects of structurally simple ligands for MT 1 and MT 2 melatonin receptors

Bioorganic & medicinal chemistry, 2010, Vol.18 (17), p.6496-6511

2010

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Synthesis and characterization of a peripherally restricted CB 1 cannabinoid antagonist, URB447, that reduces feeding and body-weight gain in mice

Bioorganic & medicinal chemistry letters, 2009, Vol.19 (3), p.639-643

2009

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Increase of brain endocannabinoid anandamide levels by FAAH inhibition and alcohol abuse behaviours in the rat: The endocannabinoid system: a modulator of brain-behavioral

Psychopharmacologia, 2008, Vol.198 (4), p.449-460

2008

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Synthesis and QSAR of Fatty Acid Amide Hydrolase Inhibitors: Modulation at the N-Portion of Biphenyl-3-yl Alkylcarbamates

Journal of medicinal chemistry, 2008-05, Vol.51 (12), p.3487-3498

2008

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Original Article: Antidepressant-like Activity of the Fatty Acid Amide Hydrolase Inhibitor URB597 in a Rat Model of Chronic Mild Stress

Biological psychiatry (1969), 2007-11, Vol.62 (10), p.1103-1110

2007

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Cover Picture: Structure-Property Relationships of a Class of Carbamate-Based Fatty Acid Amide Hydrolase (FAAH) Inhibitors: Chemical and Biological Stability / A Second Generation of Carbamate-Based Fatty Acid Amide Hydrolase Inhibitors with Improved Activity in vivo (ChemMedChem 9/2009)

ChemMedChem, 2009-09, Vol.4 (9), p.1385-1385

2009

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Erratum: Selective inhibition of 2-AG hydrolysis enhances endocannabinoid signaling in hippocampus

Nature neuroscience, 2007-01, Vol.10 (1), p.134-134

2007

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Identification of a Bioactive Impurity in a Commercial Sample of 6-Methyl-2-p-Tolylaminobenzo[d][1,3]Oxazin-4-One (URB754)

Annali di chimica, 2007-09, Vol.97 (9), p.887-894

2007

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Questionnaire

Contemporary French and francophone studies, 2008-01, Vol.12 (1), p.123-128

2008

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Design, synthesis, and pharmacological effects of structurally simple ligands for MT(1) and MT(2) melatonin receptors

Bioorganic & medicinal chemistry, 2010-09, Vol.18 (17), p.6496-6511

2010

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Synthesis and Biological Evaluation of a [gamma]-Cyclodextrin-based Formulation of the Anticancer Agent 5,6,11,12,17,18,23,24- Octahydrocyclododeca[1,2-b:4,5-b':7,8-b'':10,11-b''']tetraindole (CTet)

Molecules (Basel, Switzerland), 2010-06, Vol.15 (6), p.4085

2010

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ChemInform Abstract: Synthesis and Characterization of a Peripherally Restricted CB1 Cannabinoid Antagonist, URB447, that Reduces Feeding and Body-Weight Gain in Mice

ChemInform, 2009-06, Vol.40 (26), p.no-no

2009

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ChemInform Abstract: Synthesis and Characterization of a Peripherally Restricted CB 1 Cannabinoid Antagonist, URB447, that Reduces Feeding and Body‐Weight Gain in Mice

ChemInform, 2009-06, Vol.40 (26)

2009

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ChemInform Abstract: Stereospecific Synthesis of Mexiletine and Related Compounds: Mitsunobu versus Williamson Reaction

ChemInform, 2001-02, Vol.32 (8), p.no-no

2001

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KV11.1 Potassium Channel and the Na+/H+ Antiporter NHE1 Modulate Adhesion-Dependent Intracellular pH in Colorectal Cancer Cells

Frontiers in pharmacology, 2020-06, Vol.11, p.848-848

2020

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Real-Time Monitoring of Solar Energetic Particles Using the Alpha Magnetic Spectrometer on the International Space Station

Instruments (Basel), 2023-12, Vol.7 (4), p.38

2023

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Multi-omics Approaches To Decipher the Impact of Diet and Host Physiology on the Mammalian Gut Microbiome

Applied and environmental microbiology, 2020-11, Vol.86 (23)

2020

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Synthesis and Biological Characterization of the New Glycolipid Lactose Undecylenate (URB1418)

The green screen: Neda and the lost voices

Synthesis and Biological Evaluation of 6-IO/I-Sucrose Monoester Glycolipids as Possible New Antifungal Agents

Gay but not Queer: Defining Liminal Post-queer Identities in Maghrebian Literature

Structural determinants of peripheral O-arylcarbamate FAAH inhibitors render them dual substrates for Abcb1 and Abcg2 and restrict their access to the brain

Erratum to: Increase of brain endocannabinoid anandamide levels by FAAH inhibition and alcohol abuse behaviours in the rat

Erratum to: increase of brain endocannabinoid anandamide levels by FAAH inhibition and alcohol abuse behaviours in the rat

Erratum: The collisional behavior of ESI-generated protonated molecules of some carbamate FAAH inhibitors isosteres and its relationships with biological activity

Design, synthesis, and pharmacological effects of structurally simple ligands for MT 1 and MT 2 melatonin receptors

Synthesis and characterization of a peripherally restricted CB 1 cannabinoid antagonist, URB447, that reduces feeding and body-weight gain in mice

Increase of brain endocannabinoid anandamide levels by FAAH inhibition and alcohol abuse behaviours in the rat: The endocannabinoid system: a modulator of brain-behavioral

Synthesis and QSAR of Fatty Acid Amide Hydrolase Inhibitors: Modulation at the N-Portion of Biphenyl-3-yl Alkylcarbamates

Original Article: Antidepressant-like Activity of the Fatty Acid Amide Hydrolase Inhibitor URB597 in a Rat Model of Chronic Mild Stress

Cover Picture: Structure-Property Relationships of a Class of Carbamate-Based Fatty Acid Amide Hydrolase (FAAH) Inhibitors: Chemical and Biological Stability / A Second Generation of Carbamate-Based Fatty Acid Amide Hydrolase Inhibitors with Improved Activity in vivo (ChemMedChem 9/2009)

Erratum: Selective inhibition of 2-AG hydrolysis enhances endocannabinoid signaling in hippocampus

Identification of a Bioactive Impurity in a Commercial Sample of 6-Methyl-2-p-Tolylaminobenzo[d][1,3]Oxazin-4-One (URB754)

Questionnaire

Design, synthesis, and pharmacological effects of structurally simple ligands for MT(1) and MT(2) melatonin receptors

Synthesis and Biological Evaluation of a [gamma]-Cyclodextrin-based Formulation of the Anticancer Agent 5,6,11,12,17,18,23,24- Octahydrocyclododeca[1,2-b:4,5-b':7,8-b'':10,11-b''']tetraindole (CTet)

ChemInform Abstract: Synthesis and Characterization of a Peripherally Restricted CB1 Cannabinoid Antagonist, URB447, that Reduces Feeding and Body-Weight Gain in Mice

ChemInform Abstract: Synthesis and Characterization of a Peripherally Restricted CB 1 Cannabinoid Antagonist, URB447, that Reduces Feeding and Body‐Weight Gain in Mice

ChemInform Abstract: Stereospecific Synthesis of Mexiletine and Related Compounds: Mitsunobu versus Williamson Reaction

KV11.1 Potassium Channel and the Na+/H+ Antiporter NHE1 Modulate Adhesion-Dependent Intracellular pH in Colorectal Cancer Cells

Real-Time Monitoring of Solar Energetic Particles Using the Alpha Magnetic Spectrometer on the International Space Station

Multi-omics Approaches To Decipher the Impact of Diet and Host Physiology on the Mammalian Gut Microbiome

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