The N‐Acylethanolamine‐Hydrolyzing Acid Amidase (NAAA)
Tsuboi, Kazuhito, Takezaki, Naoko, Ueda, Natsuo·2007·Chemistry & Biodiversity
Cited by (185)
Items 101–185 of 185
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- N-Acylethanolamine Acid Amidase (NAAA): Mechanism of Palmitoylethanolamide Hydrolysis Revealed by Mechanistic SimulationsLaura Scalvini, Andrea Ghidini, Alessio Lodola, Donatella Callegari, Silvia Rivara, Daniele Piomelli, Marco Mor · 2020 · ACS Catalysis
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- Novel activity-based probes for N-acylethanolamine acid amidaseRita Petracca, Elisa Romeo, Marc P. Baggelaar, Marta Artola, Silvia Pontis, Stefano Ponzano, Herman S. Overkleeft, Mario van der Stelt, Daniele Piomelli · 2017 · Chemical Communications
- Synthesis, biological evaluation, and structure activity relationship (SAR) study of pyrrolidine amide derivatives as N -acylethanolamine acid amidase (NAAA) inhibitorsPan Zhou, Lei Xiang, Dongsheng Zhao, Jie Ren, Yan Qiu, Yuhang Li · 2018 · MedChemComm
- Synthesis and Preliminary Evaluation of N-(16-18F-Fluorohexadecanoyl)ethanolamine (18F-FHEA) as a PET Probe of N-Acylethanolamine Metabolism in Mouse BrainMukesh K. Pandey, Timothy R. DeGrado, Kun Qian, Mark Jacobson, Clinton E. Hagen, Richard I. Duclos, S. John Gatley · 2014 · ACS Chemical Neuroscience
- Inhibition of N-acylethanolamine-hydrolyzing acid amidase reduces T cell infiltration in a mouse model of multiple sclerosisStefania Sgroi, Elisa Romeo, Paolo Di Fruscia, Pier Francesca Porceddu, Debora Russo, Natalia Realini, Ennio Albanesi, Tiziano Bandiera, Fabio Bertozzi, Angelo M. Reggiani · 2021 · Pharmacological Research
- Effect of Oleoylethanolamide-Based Dietary Supplement on Systemic Inflammation in the Development of Alimentary-Induced Obesity in MiceDarya Ivashkevich, Arina I. Ponomarenko, Igor Manzhulo, Ruslan M. Sultanov, Inessa V. Dyuizen · 2023 · Nutrients
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- Design and Structure–Activity Relationships of Isothiocyanates as Potent and Selective N-Acylethanolamine-Hydrolyzing Acid Amidase InhibitorsMichael S. Malamas, Spiro Pavlopoulos, Shakiru O. Alapafuja, Shrouq I. Farah, Alexander M. Zvonok, Khadijah Ahmad Mohammad, Jay M. West, Nicholas Thomas Perry, Dimitrios N. Pelekoudas, Girija Rajarshi et al. · 2021 · Journal of Medicinal Chemistry
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- Insights in the Mechanism of Action and Inhibition of N-Acylethanolamine Acid Amidase by Means of Computational MethodsAlessio Lodola, Silvia Rivara, Marco Mor · 2014 · Advances in protein chemistry and structural biology
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- BindingDB Entry 50030672: beta-Lactams derived from a carbapenem chiron are selective inhibitors of human fatty acid amide hydrolase versus human monoacylglycerol lipase.BindingDB · 2010 · UC San Diego
- BindingDB Entry 50039848: Lipophilic amines as potent inhibitors of N-acylethanolamine-hydrolyzing acid amidase.BindingDB · 2013 · UC San Diego
- BindingDB Entry 50014558: Discovery and SAR Evolution of Pyrazole Azabicyclo[3.2.1]octane Sulfonamides as a Novel Class of Non-CovalentBindingDB · 2022 · UC San Diego
- BindingDB Entry 50041828: Synthesis and structure-activity relationships of N-(2-oxo-3-oxetanyl)amides as N-acylethanolamine-hydrolyzing acid amidase inhibitors.BindingDB · 2013 · UC San Diego
- BindingDB Entry 50010439: Design and synthesis of cyanamides as potent and selective N-acylethanolamine acid amidase inhibitors.BindingDB · 2021 · UC San Diego
- BindingDB Entry 50040134: ß-Lactones Inhibit N-acylethanolamine Acid Amidase by S-Acylation of the Catalytic N-Terminal Cysteine.BindingDB · 2013 · UC San Diego
- BindingDB Entry 50014428: Design and Structure-Activity Relationships of Isothiocyanates as Potent and SelectiveBindingDB · 2022 · UC San Diego
- BindingDB Entry 50045459: Novel tail and head group prostamide probes.BindingDB · 2016 · UC San Diego
- BindingDB Entry 50047146: Potenta-amino-ß-lactam carbamic acid ester as NAAA inhibitors. Synthesis and structure-activity relationship (SAR) studies.BindingDB · 2017 · UC San Diego
- BindingDB Entry 50043348: Synthesis and structure-activity relationship (SAR) of 2-methyl-4-oxo-3-oxetanylcarbamic acid esters, a class of potent N-acylethanolamine acid amidase (NAAA) inhibitors.BindingDB · 2014 · UC San Diego
- BindingDB Entry 50001937: Therapeutic Potential of Fatty Acid Amide Hydrolase, Monoacylglycerol Lipase, and N-Acylethanolamine Acid Amidase Inhibitors.BindingDB · 2020 · UC San Diego
- BindingDB Entry 50044840: Synthesis, biological evaluation, and 3D QSAR study of 2-methyl-4-oxo-3-oxetanylcarbamic acid esters as N-acylethanolamine acid amidase (NAAA) inhibitors.BindingDB · 2016 · UC San Diego
- BindingDB Entry 50040090: N-(2-oxo-3-oxetanyl)carbamic acid esters as N-acylethanolamine acid amidase inhibitors: synthesis and structure-activity and structure-property relationships.BindingDB · 2013 · UC San Diego
- BindingDB Entry 50049118: Progress in the development ofß-lactams as N-Acylethanolamine Acid Amidase (NAAA) inhibitors: Synthesis and SAR study of new, potent N-O-substituted derivatives.BindingDB · 2019 · UC San Diego