The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
28182408 |
126 |
Design, Synthesis, Structure-Activity Relationship Studies, and Three-Dimensional Quantitative Structure-Activity Relationship (3D-QSAR) Modeling of a Series of O-Biphenyl Carbamates as Dual Modulators of Dopamine D3 Receptor and Fatty Acid Amide Hydrolase.![EBI](/images/logo_chembl.png) |
Universit£ |
27989417 |
34 |
1-Heteroarylpropan-2-ones as inhibitors of fatty acid amide hydrolase: Studies on structure-activity relationships and metabolic stability.![EBI](/images/logo_chembl.png) |
University of M£Nster |
27309570 |
102 |
Fatty Acid Amide Hydrolase (FAAH), Acetylcholinesterase (AChE), and Butyrylcholinesterase (BuChE): Networked Targets for the Development of Carbamates as Potential Anti-Alzheimer's Disease Agents.![EBI](/images/logo_chembl.png) |
Alma Mater Studiorum-University of Bologna |
27189675 |
38 |
The SAR of brain penetration for a series of heteroaryl urea FAAH inhibitors.![EBI](/images/logo_chembl.png) |
Janssen Pharmaceutical Companies of Johnson & Johnson |
27117424 |
7 |
Design, synthesis and biological evaluation of potent FAAH inhibitors.![EBI](/images/logo_chembl.png) |
Univ. Lille |
26888301 |
34 |
Development and Pharmacological Characterization of Selective Blockers of 2-Arachidonoyl Glycerol Degradation with Efficacy in Rodent Models of Multiple Sclerosis and Pain.![EBI](/images/logo_chembl.png) |
University of Siena |
26774927 |
120 |
Potent multitarget FAAH-COX inhibitors: Design and structure-activity relationship studies.![EBI](/images/logo_chembl.png) |
Fondazione Istituto Italiano Di Tecnologia |
26850005 |
89 |
Arylboronic acids as dual-action FAAH and TRPV1 ligands.![EBI](/images/logo_chembl.png) |
Sapienza University of Rome |
25701254 |
48 |
Novel tail and head group prostamide probes.![EBI](/images/logo_chembl.png) |
Northeastern University |
25065940 |
77 |
Structure-affinity relationships and pharmacological characterization of new alkyl-resorcinol cannabinoid receptor ligands: Identification of a dual cannabinoid receptor/TRPA1 channel agonist.![EBI](/images/logo_chembl.png) |
Universit£ |
25037918 |
33 |
Discovery libraries targeting the major enzyme classes: the serine hydrolases.![EBI](/images/logo_chembl.png) |
The Scripps Research Institute |
24944750 |
24 |
Discovery of MK-4409, a Novel Oxazole FAAH Inhibitor for the Treatment of Inflammatory and Neuropathic Pain.![EBI](/images/logo_chembl.png) |
Merck Research Laboratories |
24690529 |
43 |
a-Ketoheterocycle inhibitors of fatty acid amide hydrolase: exploration of conformational constraints in the acyl side chain.![EBI](/images/logo_chembl.png) |
The Scripps Research Institute |
24456116 |
105 |
Design, synthesis, and characterization ofa-ketoheterocycles that additionally target the cytosolic port Cys269 of fatty acid amide hydrolase.![EBI](/images/logo_chembl.png) |
The Scripps Research Institute |
24513048 |
88 |
1-Aryl-2-((6-aryl)pyrimidin-4-yl)amino)ethanols as competitive inhibitors of fatty acid amide hydrolase.![EBI](/images/logo_chembl.png) |
Janssen Pharmaceutical Companies of Johnson & Johnson |
24440478 |
22 |
Design, synthesis, and biological evaluation of a series of piperazine ureas as fatty acid amide hydrolase inhibitors.![EBI](/images/logo_chembl.png) |
Takeda Pharmaceutical |
24433863 |
76 |
Heteroarylureas with spirocyclic diamine cores as inhibitors of fatty acid amide hydrolase.![EBI](/images/logo_chembl.png) |
Janssen Research and Development |
24083878 |
61 |
Chiral 1,3,4-oxadiazol-2-ones as highly selective FAAH inhibitors.![EBI](/images/logo_chembl.png) |
University of Eastern Finland |
23822179 |
17 |
Synthesis and structure-activity relationship studies of O-biphenyl-3-yl carbamates as peripherally restricted fatty acid amide hydrolase inhibitors.![EBI](/images/logo_chembl.png) |
Fondazione Istituto Italiano Di Tecnologia |
23712084 |
2 |
Development and characterization of a promising fluorine-18 labelled radiopharmaceutical for in vivo imaging of fatty acid amide hydrolase.![EBI](/images/logo_chembl.png) |
Centre For Addiction and Mental Health |
24900701 |
36 |
Discovery of MK-3168: A PET Tracer for Imaging Brain Fatty Acid Amide Hydrolase.![EBI](/images/logo_chembl.png) |
Merck Research Laboratories |
23474898 |
161 |
Biaryl tetrazolyl ureas as inhibitors of endocannabinoid metabolism: modulation at the N-portion and distal phenyl ring.![EBI](/images/logo_chembl.png) |
Sapienza University of Rome |
23455058 |
84 |
(4-Phenoxyphenyl)tetrazolecarboxamides and related compounds as dual inhibitors of fatty acid amide hydrolase (FAAH) and monoacylglycerol lipase (MAGL).![EBI](/images/logo_chembl.png) |
University of M£Nster |
23218778 |
49 |
Synthesis, SAR study, and biological evaluation of a series of piperazine ureas as fatty acid amide hydrolase (FAAH) inhibitors.![EBI](/images/logo_chembl.png) |
Takeda Pharmaceutical |
23214511 |
4 |
Radiosynthesis and evaluation of [¹¹C-carbonyl]-labeled carbamates as fatty acid amide hydrolase radiotracers for positron emission tomography.![EBI](/images/logo_chembl.png) |
Centre For Addiction and Mental Health |
23206861 |
113 |
Tetrahydro-ß-carboline derivatives targeting fatty acid amide hydrolase (FAAH) and transient receptor potential (TRP) channels.![EBI](/images/logo_chembl.png) |
Sapienza University of Rome |
21820769 |
20 |
Biphenyl-3-yl alkylcarbamates as fatty acid amide hydrolase (FAAH) inhibitors: steric effects of N-alkyl chain on rat plasma and liver stability.![EBI](/images/logo_chembl.png) |
Universit£ |
19719235 |
19 |
Synthesis, in vitro and in vivo evaluation, and radiolabeling of aryl anandamide analogues as candidate radioligands for in vivo imaging of fatty acid amide hydrolase in the brain.![EBI](/images/logo_chembl.png) |
Ghent University |
23141911 |
60 |
Heteroaryl urea inhibitors of fatty acid amide hydrolase: structure-mutagenicity relationships for arylamine metabolites.![EBI](/images/logo_chembl.png) |
Janssen Research and Development |
23043222 |
125 |
Identification and characterization of carprofen as a multitarget fatty acid amide hydrolase/cyclooxygenase inhibitor.![EBI](/images/logo_chembl.png) |
Istituto Italiano Di Tecnologia |
22738638 |
59 |
Assay and inhibition of diacylglycerol lipase activity.![EBI](/images/logo_chembl.png) |
Northeastern University |
24900385 |
51 |
Aryl Piperazinyl Ureas as Inhibitors of Fatty Acid Amide Hydrolase (FAAH) in Rat, Dog, and Primate.![EBI](/images/logo_chembl.png) |
TBA |
24900454 |
43 |
The First Dual ChE/FAAH Inhibitors: New Perspectives for Alzheimer's Disease?![EBI](/images/logo_chembl.png) |
TBA |
22185522 |
159 |
Structure-activity relationship of a new series of reversible dual monoacylglycerol lipase/fatty acid amide hydrolase inhibitors.![EBI](/images/logo_chembl.png) |
Universidad Complutense De Madrid |
21666860 |
14 |
Discovery of PF-04457845: A Highly Potent, Orally Bioavailable, and Selective Urea FAAH Inhibitor.![EBI](/images/logo_chembl.png) |
Pfizer |
18983142 |
135 |
Discovery and development of fatty acid amide hydrolase (FAAH) inhibitors.![EBI](/images/logo_chembl.png) |
Johnson & Johnson Pharmaceutical Research and Development |
18630870 |
236 |
Optimization of the central heterocycle of alpha-ketoheterocycle inhibitors of fatty acid amide hydrolase.![EBI](/images/logo_chembl.png) |
Institute For Chemical Biology |
18424134 |
114 |
New tetrazole-based selective anandamide uptake inhibitors.![EBI](/images/logo_chembl.png) |
Sapienza University of Rome |
18053726 |
364 |
Inhibitors of proteases and amide hydrolases that employ an alpha-ketoheterocycle as a key enabling functionality.![EBI](/images/logo_chembl.png) |
Johnson & Johnson Pharmaceutical Research & Development |
18247553 |
174 |
Optimization of alpha-ketooxazole inhibitors of fatty acid amide hydrolase.![EBI](/images/logo_chembl.png) |
The Scripps Research Institute |
17561406 |
67 |
Design, synthesis, binding, and molecular modeling studies of new potent ligands of cannabinoid receptors.![EBI](/images/logo_chembl.png) |
Universit£ |
16279794 |
46 |
Design, synthesis, and binding studies of new potent ligands of cannabinoid receptors.![EBI](/images/logo_chembl.png) |
Universit£ |
16213718 |
93 |
New metabolically stable fatty acid amide ligands of cannabinoid receptors: Synthesis and receptor affinity studies.![EBI](/images/logo_chembl.png) |
Institute of Biomolecular Chemistry |
16078824 |
48 |
The endocannabinoid system: drug targets, lead compounds, and potential therapeutic applications.![EBI](/images/logo_chembl.png) |
Universit£ |
12672252 |
104 |
Design, synthesis, and biological evaluation of new inhibitors of the endocannabinoid uptake: comparison with effects on fatty acid amidohydrolase.![EBI](/images/logo_chembl.png) |
Universidad Complutense |
22209458 |
114 |
Fatty acid amide hydrolase inhibitors. 3: tetra-substituted azetidine ureas with in vivo activity.![EBI](/images/logo_chembl.png) |
Vernalis (R&D) |
22196515 |
14 |
Design, synthesis and evaluation of polar head group containing 2-keto-oxazole inhibitors of FAAH.![EBI](/images/logo_chembl.png) |
Max Planck Institute of Molecular Physiology |
21764305 |
79 |
The discovery and development of inhibitors of fatty acid amide hydrolase (FAAH).![EBI](/images/logo_chembl.png) |
The Scripps Research Institute |
21428410 |
78 |
Reversible competitivea-ketoheterocycle inhibitors of fatty acid amide hydrolase containing additional conformational constraints in the acyl side chain: orally active, long-acting analgesics.![EBI](/images/logo_chembl.png) |
The Scripps Research Institute |
21392988 |
87 |
Identification of potent, noncovalent fatty acid amide hydrolase (FAAH) inhibitors.![EBI](/images/logo_chembl.png) |
Amgen |
19875281 |
73 |
Synthesis and biological evaluation of piperazinyl carbamates and ureas as fatty acid amide hydrolase (FAAH) and transient receptor potential (TRP) channel dual ligands.![EBI](/images/logo_chembl.png) |
Sapienza University of Rome |
19850474 |
5 |
Mining biologically-active molecules for inhibitors of fatty acid amide hydrolase (FAAH): identification of phenmedipham and amperozide as FAAH inhibitors.![EBI](/images/logo_chembl.png) |
Renovis |
20005725 |
61 |
1-Indol-1-yl-propan-2-ones and related heterocyclic compounds as dual inhibitors of cytosolic phospholipase A(2)alpha and fatty acid amide hydrolase.![EBI](/images/logo_chembl.png) |
University of M£Nster |
20143779 |
28 |
Synthesis and evaluation of paracetamol esters as novel fatty acid amide hydrolase inhibitors.![EBI](/images/logo_chembl.png) |
University of Cagliari |
19924997 |
2 |
X-ray crystallographic analysis of alpha-ketoheterocycle inhibitors bound to a humanized variant of fatty acid amide hydrolase.![EBI](/images/logo_chembl.png) |
The Scripps Research Institute |
19539407 |
18 |
Chiral 3-(4,5-dihydrooxazol-2-yl)phenyl alkylcarbamates as novel FAAH inhibitors: Insight into FAAH enantioselectivity by molecular docking and interaction fields.![EBI](/images/logo_chembl.png) |
Helsinki University of Technology |
19515560 |
24 |
Fatty acid amide hydrolase inhibitors. Surprising selectivity of chiral azetidine ureas.![EBI](/images/logo_chembl.png) |
Vernalis (R&D) |
19232787 |
71 |
The synthesis and biological evaluation of para-substituted phenolic N-alkyl carbamates as endocannabinoid hydrolyzing enzyme inhibitors.![EBI](/images/logo_chembl.png) |
University of Kuopio |
19054678 |
12 |
Radiosynthesis, in vitro and in vivo evaluation of 123I-labeled anandamide analogues for mapping brain FAAH.![EBI](/images/logo_chembl.png) |
Ghent University |
18831576 |
66 |
Tetrahydrolipstatin analogues as modulators of endocannabinoid 2-arachidonoylglycerol metabolism.![EBI](/images/logo_chembl.png) |
Sapienza University of Rome |
18693015 |
85 |
Thiadiazolopiperazinyl ureas as inhibitors of fatty acid amide hydrolase.![EBI](/images/logo_chembl.png) |
Johnson & Johnson Pharmaceutical Research and Development |
18639454 |
55 |
Exploration of a fundamental substituent effect of alpha-ketoheterocycle enzyme inhibitors: Potent and selective inhibitors of fatty acid amide hydrolase.![EBI](/images/logo_chembl.png) |
The Scripps Research Institute |
18507372 |
31 |
Synthesis and quantitative structure-activity relationship of fatty acid amide hydrolase inhibitors: modulation at the N-portion of biphenyl-3-yl alkylcarbamates.![EBI](/images/logo_chembl.png) |
Università |
17452063 |
30 |
Carbamoyl tetrazoles as inhibitors of endocannabinoid inactivation: a critical revisitation.![EBI](/images/logo_chembl.png) |
Sapienza University of Rome |
17764163 |
61 |
Structure-activity relationship of a series of inhibitors of monoacylglycerol hydrolysis--comparison with effects upon fatty acid amide hydrolase.![EBI](/images/logo_chembl.png) |
Universidad Complutense |
17665899 |
16 |
Design, synthesis, and in vitro evaluation of carbamate derivatives of 2-benzoxazolyl- and 2-benzothiazolyl-(3-hydroxyphenyl)-methanones as novel fatty acid amide hydrolase inhibitors.![EBI](/images/logo_chembl.png) |
Helsinki University of Technology |
16854070 |
12 |
Fatty acid amide hydrolase inhibitors from virtual screening of the endocannabinoid system.![EBI](/images/logo_chembl.png) |
University of Kuopio |
16570928 |
16 |
Development of the first potential covalent inhibitors of anandamide cellular uptake.![EBI](/images/logo_chembl.png) |
Institute of Biomolecular Chemistry |
15771430 |
129 |
Discovery of a potent, selective, and efficacious class of reversible alpha-ketoheterocycle inhibitors of fatty acid amide hydrolase effective as analgesics.![EBI](/images/logo_chembl.png) |
The Scripps Research Institute |
15582420 |
37 |
Heterocyclic sulfoxide and sulfone inhibitors of fatty acid amide hydrolase.![EBI](/images/logo_chembl.png) |
The Scripps Research Institute |
15456244 |
25 |
Cyclohexylcarbamic acid 3'- or 4'-substituted biphenyl-3-yl esters as fatty acid amide hydrolase inhibitors: synthesis, quantitative structure-activity relationships, and molecular modeling studies.![EBI](/images/logo_chembl.png) |
Università |
12951114 |
18 |
Arachidonylsulfonyl derivatives as cannabinoid CB1 receptor and fatty acid amide hydrolase inhibitors.![EBI](/images/logo_chembl.png) |
University of California |
12781177 |
7 |
Hemisynthesis and preliminary evaluation of novel endocannabinoid analogues.![EBI](/images/logo_chembl.png) |
Umr Cnrs 5074 |
12773040 |
41 |
Design, synthesis, and structure-activity relationships of alkylcarbamic acid aryl esters, a new class of fatty acid amide hydrolase inhibitors.![EBI](/images/logo_chembl.png) |
Università |
11412972 |
13 |
alpha-Keto heterocycle inhibitors of fatty acid amide hydrolase: carbonyl group modification and alpha-substitution.![EBI](/images/logo_chembl.png) |
The Scripps Research Institute |
32429662 |
39 |
Discovery of Aryl Formyl Piperidine Derivatives as Potent, Reversible, and Selective Monoacylglycerol Lipase Inhibitors.![EBI](/images/logo_chembl.png) |
China Pharmaceutical University |
30816712 |
78 |
Plant-Based Modulators of Endocannabinoid Signaling.![EBI](/images/logo_chembl.png) |
Concordia University Wisconsin |
30446439 |
64 |
Synthesis and evaluation of potent and selective MGL inhibitors as a glaucoma treatment.![EBI](/images/logo_chembl.png) |
Mak Scientific |
30340141 |
64 |
Tetrazolylpropan-2-ones as inhibitors of fatty acid amide hydrolase: Studies on structure-activity relationships and metabolic stability.![EBI](/images/logo_chembl.png) |
University of M£Nster |
10021942 |
46 |
Trifluoromethyl ketone inhibitors of fatty acid amide hydrolase: a probe of structural and conformational features contributing to inhibition.![EBI](/images/logo_chembl.png) |
Scripps Research Institute |
30503633 |
73 |
Discovery and evaluation of novel FAAH inhibitors in neuropathic pain model.![EBI](/images/logo_chembl.png) |
Advinus Therapeutics |
31629610 |
96 |
Piperidine and piperazine inhibitors of fatty acid amide hydrolase targeting excitotoxic pathology.![EBI](/images/logo_chembl.png) |
Northeastern University |
31714779 |
37 |
Benzisothiazolinone Derivatives as Potent Allosteric Monoacylglycerol Lipase Inhibitors That Functionally Mimic Sulfenylation of Regulatory Cysteines.![EBI](/images/logo_chembl.png) |
Universit£ |
31407888 |
4 |
New Approaches to Cancer Therapy: Combining Fatty Acid Amide Hydrolase (FAAH) Inhibition with Peroxisome Proliferator-Activated Receptors (PPARs) Activation.![EBI](/images/logo_chembl.png) |
Universit£ |
30126274 |
44 |
Identification of Bivalent Ligands with Melatonin Receptor Agonist and Fatty Acid Amide Hydrolase (FAAH) Inhibitory Activity That Exhibit Ocular Hypotensive Effect in the Rabbit.![EBI](/images/logo_chembl.png) |
Universit£ |
29366648 |
98 |
Identification and optimization of soluble epoxide hydrolase inhibitors with dual potency towards fatty acid amide hydrolase.![EBI](/images/logo_chembl.png) |
University of California Davis |
27766867 |
109 |
Therapeutic Potential of Fatty Acid Amide Hydrolase, Monoacylglycerol Lipase, and N-Acylethanolamine Acid Amidase Inhibitors.![EBI](/images/logo_chembl.png) |
Universit£ |
28535469 |
69 |
Novel propanamides as fatty acid amide hydrolase inhibitors.![EBI](/images/logo_chembl.png) |
University of Cagliari |
23839942 |
19 |
Heterodimerization with Its splice variant blocks the ghrelin receptor 1a in a non-signaling conformation: a study with a purified heterodimer assembled into lipid discs.![BDB](/images/logo_bindingdb.png) |
Université Montpellier 1 |
7590751 |
11 |
The cloning and chromosomal mapping of two novel human opioid-somatostatin-like receptor genes, GPR7 and GPR8, expressed in discrete areas of the brain.![BDB](/images/logo_bindingdb.png) |
Addiction Research Foundation |
3010074 |
129 |
Characterization of the A2 adenosine receptor labeled by [3H]NECA in rat striatal membranes.![BDB](/images/logo_bindingdb.png) |
Warner-Lambert/Parke-Davis Pharmaceutical Research |
19374401 |
103 |
Discovery of inducible nitric oxide synthase (iNOS) inhibitor development candidate KD7332, part 1: Identification of a novel, potent, and selective series of quinolinone iNOS dimerization inhibitors that are orally active in rodent pain models.![BDB](/images/logo_bindingdb.png) |
Kalypsys |
8765511 |
14 |
Nonpeptidal P2 ligands for HIV protease inhibitors: structure-based design, synthesis, and biological evaluation.![BDB](/images/logo_bindingdb.png) |
University of Illinois At Chicago |