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Antinociceptive effects of the N-acylethanolamine acid amidase inhibitor ARN077 in rodent pain models

Pain (Amsterdam), 2013-03, Vol.154 (3), p.350-360

2013

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Modulation of anxiety through blockade of anandamide hydrolysis

Nature medicine, 2003-01, Vol.9 (1), p.76-81

2003

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Inhibition of Fatty Acid Amide Hydrolase (FAAH) Regulates NF-kb Pathways Reducing Bleomycin-Induced Chronic Lung Inflammation and Pulmonary Fibrosis

International journal of molecular sciences, 2023-06, Vol.24 (12), p.10125

2023

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Fatty Acid Amide Hydrolase (FAAH) Inhibition Plays a Key Role in Counteracting Acute Lung Injury

International journal of molecular sciences, 2022-03, Vol.23 (5), p.2781

2022

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Endocannabinoid regulation of acute and protracted nicotine withdrawal: effect of FAAH inhibition

PloS one, 2011-11, Vol.6 (11), p.e28142

2011

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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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Induction of endoplasmic reticulum stress response by the indole-3-carbinol cyclic tetrameric derivative CTet in human breast cancer cell lines

PloS one, 2012-08, Vol.7 (8), p.e43249-e43249

2012

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

Nature neuroscience, 2005-09, Vol.8 (9), p.1139-1141

2005

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Indole-3-carbinol in vitro antiviral activity against SARS-Cov-2 virus and in vivo toxicity

Cell death discovery, 2022-12, Vol.8 (1), p.491-491, Article 491

2022

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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.4085-4093

2010

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Anandamide suppresses pain initiation through a peripheral endocannabinoid mechanism

Nature neuroscience, 2010-10, Vol.13 (10), p.1265-1270

2010

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Tandem mass spectrometric data-FAAH inhibitory activity relationships of some carbamic acid O-aryl esters

Journal of mass spectrometry, 2004-12, Vol.39 (12), p.1450-1455

2004

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The influence of mannose-based esters on the mesophase behaviour of lyotropic liquid crystalline nanosystems as drug delivery vectors

Colloids and surfaces, B, Biointerfaces, 2023-12, Vol.232, p.113596-113596, Article 113596

2023

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An endocannabinoid mechanism for stress-induced analgesia

Nature, 2005-06, Vol.435 (7045), p.1108-1112

2005

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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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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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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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Stereospecific synthesis of mexiletine and related compounds: Mitsunobu versus Williamson reaction

Tetrahedron: asymmetry, 2000-09, Vol.11 (17), p.3619-3634

2000

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Inhibition of anandamide hydrolysis enhances noradrenergic and GABAergic transmission in the prefrontal cortex and basolateral amygdala of rats subjected to acute swim stress

Journal of neuroscience research, 2015-05, Vol.93 (5), p.777-787

2015

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Pretreatment with the monoacylglycerol lipase inhibitor URB602 protects from the long-term consequences of neonatal hypoxic―ischemic brain injury in rats

Pediatric research, 2012-10, Vol.72 (4), p.400-406

2012

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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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The Indole-3-carbinol cyclic tetrameric derivative CTet synergizes with cisplatin and doxorubicin in triple-negative breast cancer cell lines

Anticancer research, 2013-05, Vol.33 (5), p.1867-1872

2013

Volltextzugriff (PDF)

The indole-3-carbinol cyclic tetrameric derivative CTet inhibits cell proliferation via overexpression of p21/CDKN1A in both estrogen receptor-positive and triple-negative breast cancer cell lines

Breast cancer research : BCR, 2011-03, Vol.13 (2), p.R33-R33, Article R33

2011

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A practical and expeditious method for the preparation of the potential 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)

Tetrahedron letters, 2011-06, Vol.52 (22), p.2812-2814

2011

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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

Volltextzugriff (PDF)

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Antinociceptive effects of the N-acylethanolamine acid amidase inhibitor ARN077 in rodent pain models

Modulation of anxiety through blockade of anandamide hydrolysis

Inhibition of Fatty Acid Amide Hydrolase (FAAH) Regulates NF-kb Pathways Reducing Bleomycin-Induced Chronic Lung Inflammation and Pulmonary Fibrosis

Fatty Acid Amide Hydrolase (FAAH) Inhibition Plays a Key Role in Counteracting Acute Lung Injury

Endocannabinoid regulation of acute and protracted nicotine withdrawal: effect of FAAH inhibition

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

Induction of endoplasmic reticulum stress response by the indole-3-carbinol cyclic tetrameric derivative CTet in human breast cancer cell lines

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

Indole-3-carbinol in vitro antiviral activity against SARS-Cov-2 virus and in vivo toxicity

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)

Anandamide suppresses pain initiation through a peripheral endocannabinoid mechanism

Tandem mass spectrometric data-FAAH inhibitory activity relationships of some carbamic acid O-aryl esters

The influence of mannose-based esters on the mesophase behaviour of lyotropic liquid crystalline nanosystems as drug delivery vectors

An endocannabinoid mechanism for stress-induced analgesia

The green screen: Neda and the lost voices

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

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

Stereospecific synthesis of mexiletine and related compounds: Mitsunobu versus Williamson reaction

Inhibition of anandamide hydrolysis enhances noradrenergic and GABAergic transmission in the prefrontal cortex and basolateral amygdala of rats subjected to acute swim stress

Pretreatment with the monoacylglycerol lipase inhibitor URB602 protects from the long-term consequences of neonatal hypoxic―ischemic brain injury in rats

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

The Indole-3-carbinol cyclic tetrameric derivative CTet synergizes with cisplatin and doxorubicin in triple-negative breast cancer cell lines

The indole-3-carbinol cyclic tetrameric derivative CTet inhibits cell proliferation via overexpression of p21/CDKN1A in both estrogen receptor-positive and triple-negative breast cancer cell lines

A practical and expeditious method for the preparation of the potential 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)

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

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