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Application of 3D-QSAR in the Rational Design of Receptor Ligands and Enzyme Inhibitors.
- Published in:
- Chemistry & Biodiversity, 2005, v. 2, n. 11, p. 1438, doi. 10.1002/cbdv.200590117
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- Article
Anandamide suppresses pain initiation through a peripheral endocannabinoid mechanism.
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- Nature Neuroscience, 2010, v. 13, n. 10, p. 1265, doi. 10.1038/nn.2632
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- Article
Selective inhibition of 2-AG hydrolysis enhances endocannabinoid signaling in hippocampus.
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- 2007
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- Correction notice
Selective inhibition of 2-AG hydrolysis enhances endocannabinoid signaling in hippocampus.
- Published in:
- Nature Neuroscience, 2005, v. 8, n. 9, p. 1139, doi. 10.1038/nn1521
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- Article
On the formation of [H<sub>3</sub>CSSCH<sub>3</sub>]<sup>+ .</sup> ions from the bis(dimethylthio)mercury molecular ion.
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- Rapid Communications in Mass Spectrometry: RCM, 2006, v. 20, n. 20, p. 3154, doi. 10.1002/rcm.2716
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- Article
The collisional behavior of ESI-generated protonated molecules of some carbamate FAAH inhibitors isosteres and its relationships with biological activity.
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- Journal of Mass Spectrometry, 2009, v. 44, n. 4, p. 561, doi. 10.1002/jms.1524
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- Article
Correlation between energetics of collisionally activated decompositions, interaction energy and biological potency of carbamate FAAH inhibitors.
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- Journal of Mass Spectrometry, 2007, v. 42, n. 12, p. 1624, doi. 10.1002/jms.1346
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- Article
Tandem mass spectrometric data-FAAH inhibitory activity relationships of some carbamic acid O-aryl esters.
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- Journal of Mass Spectrometry, 2004, v. 39, n. 12, p. 1450, doi. 10.1002/jms.729
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- Article
Electron impact ionization and fast atom bombardment mass spectrometry of some 3,3-dimethyl-1-(isoxazol-3-yl)triazenes, a new class of potential anticancer agents.
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- Journal of Mass Spectrometry, 1995, v. 30, n. 11, p. 1567, doi. 10.1002/jms.1190301108
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- Article
Pharmacokinetics, pharmacodynamics and safety studies on URB937, a peripherally restricted fatty acid amide hydrolase inhibitor, in rats.
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- Journal of Pharmacy & Pharmacology, 2019, v. 71, n. 12, p. 1762, doi. 10.1111/jphp.13166
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- Article
4,5-Dihydroisoxazole and 4,5-dihydro-1,2,4-oxadiazole derivatives from cycloaddition reactions of nitrile oxides to alkyl N-(diphenylmethylene)-α,β-dehydroamino acids.
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- Journal of Heterocyclic Chemistry, 1992, v. 29, n. 6, p. 1593, doi. 10.1002/jhet.5570290637
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- Publication type:
- Article
Pyrrolopyridine analogs of nalidixic acid. 2. Pyrrolo[3,4-6]pyridines.
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- Journal of Heterocyclic Chemistry, 1986, v. 23, n. 5, p. 1561, doi. 10.1002/jhet.5570230561
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- Publication type:
- Article
Pyrrolopyridine analogs of nalidixic acid. 1. Pyrrolo[2,3- b]pyridines.
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- Journal of Heterocyclic Chemistry, 1986, v. 23, n. 5, p. 1555, doi. 10.1002/jhet.5570230560
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- Publication type:
- Article
Correlation of the antimetastatic properties of aryltriazenes with their electron impact ionization mass spectrometry.
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- Rapid Communications in Mass Spectrometry: RCM, 1997, v. 11, n. 12, p. 1365, doi. 10.1002/(SICI)1097-0231(199708)11:12<1365::AID-RCM961>3.0.CO;2-M
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- Publication type:
- Article
Letter to the Editor: Correlation of the mutagenic properties of aryl- and heteroaryltriazenes with their electron ionization induced fragmentation.
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- Rapid Communications in Mass Spectrometry: RCM, 1996, v. 10, n. 9, p. 1156, doi. 10.1002/(SICI)1097-0231(19960715)10:9<1156::AID-RCM586>3.0.CO;2-N
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- Article
Modulation of anxiety through blockade of anandamide hydrolysis.
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- Nature Medicine, 2003, v. 9, n. 1, p. 76, doi. 10.1038/nm803
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- Article
Promotion of Non-Rapid Eye Movement Sleep and Activation of Reticular Thalamic Neurons by a Novel MT<sub>2</sub> Melatonin Receptor Ligand.
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- Journal of Neuroscience, 2011, v. 31, n. 50, p. 18439, doi. 10.1523/JNEUROSCI.2676-11.2011
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- Article
Oleylethanolamide regulates feeding and body weight through activation of the nuclear receptor PPAR-a.
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- Nature, 2003, v. 425, n. 6953, p. 90, doi. 10.1038/nature01921
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- Publication type:
- Article
2-(1,1'-biphenyl-4-yl)-1,2,4-triazole[5,1-a] isoquinoline (L 14105), a potential orally active contragestational agent for the bitch: studies in the rat, hamster and dog.
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- Journal of Veterinary Pharmacology & Therapeutics, 1986, v. 9, n. 3, p. 246, doi. 10.1111/j.1365-2885.1986.tb00038.x
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- Article
Melatonin antagonizes apoptosis via receptor interaction in U937 monocytic cells.
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- Journal of Pineal Research, 2007, v. 43, n. 2, p. 154, doi. 10.1111/j.1600-079X.2007.00455.x
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- Article
Synthesis, antioxidant activity and structure–activity relationships for a new series of 2-( N-acylaminoethyl)indoles with melatonin-like cytoprotective activity.
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- Journal of Pineal Research, 2006, v. 40, n. 3, p. 259, doi. 10.1111/j.1600-079X.2005.00309.x
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- Publication type:
- Article
Melatonin prevents apoptosis induced by UV-B treatment in U937 cell line.
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- Journal of Pineal Research, 2006, v. 40, n. 2, p. 158, doi. 10.1111/j.1600-079X.2005.00293.x
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- Article
Indole-based analogs of melatonin: in vitro antioxidant and cytoprotective activities.
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- Journal of Pineal Research, 2004, v. 36, n. 2, p. 95, doi. 10.1046/j.1600-079X.2003.00102.x
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- Publication type:
- Article
A new melatonin receptor ligand with mt1-agonist and MT2-antagonist properties.
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- Journal of Pineal Research, 2000, v. 29, n. 4, p. 234, doi. 10.1034/j.1600-0633.2002.290406.x
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- Publication type:
- Article
Potent, Metabolically Stable 2-Alkyl-8-(2 H-1,2,3-triazol-2-yl)-9 H-adenines as Adenosine A<sub>2A</sub> Receptor Ligands.
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- ChemMedChem, 2015, v. 10, n. 7, p. 1149, doi. 10.1002/cmdc.201500113
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- Publication type:
- Article
3-Aminoazetidin-2-one Derivatives as N-Acylethanolamine Acid Amidase (NAAA) Inhibitors Suitable for Systemic Administration.
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- ChemMedChem, 2014, v. 9, n. 7, p. 1602, doi. 10.1002/cmdc.201300546
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- Article
Editorial: Premature Publishing and Over-fragmentation.
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- ChemMedChem, 2013, v. 8, n. 1, p. 6, doi. 10.1002/cmdc.201200494
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- Article
MT<sub>1</sub>-Selective Melatonin Receptor Ligands: Synthesis, Pharmacological Evaluation, and Molecular Dynamics Investigation of N-{[(3- O-Substituted)anilino]alkyl}amides.
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- ChemMedChem, 2012, v. 7, n. 11, p. 1954, doi. 10.1002/cmdc.201200303
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- Article
N-(Anilinoethyl)amides: Design and Synthesis of Metabolically Stable, Selective Melatonin Receptor Ligands.
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- ChemMedChem, 2009, v. 4, n. 10, p. 1746, doi. 10.1002/cmdc.200900240
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- Article
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)
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- ChemMedChem, 2009, v. 4, n. 9, p. 1385, doi. 10.1002/cmdc.200990041
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- Article
Structure-Property Relationships of a Class of Carbamate-Based Fatty Acid Amide Hydrolase (FAAH) Inhibitors: Chemical and Biological Stability.
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- ChemMedChem, 2009, v. 4, n. 9, p. 1495, doi. 10.1002/cmdc.200900120
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- Publication type:
- Article
A Second Generation of Carbamate-Based Fatty Acid Amide Hydrolase Inhibitors with Improved Activity in vivo.
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- ChemMedChem, 2009, v. 4, n. 9, p. 1505, doi. 10.1002/cmdc.200900210
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- Article
Medicinal Chemistry: Defining Itself.
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- ChemMedChem, 2008, v. 3, n. 8, p. 1147, doi. 10.1002/cmdc.200800116
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- Article
Synthesis, Enantiomeric Resolution, and Structure-Activity Relationship Study of a Series of 10,11-Dihydro-5 H-Dibenzo[a,d]cycloheptene MT<sub>2</sub> Receptor Antagonists.
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- ChemMedChem, 2007, v. 2, n. 12, p. 1741, doi. 10.1002/cmdc.200700141
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- Article
Towards the Development of Mixed MT<sub>1</sub>-Agonist/MT<sub>2</sub>-Antagonist Melatonin Receptor Ligands.
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- ChemMedChem, 2006, v. 1, n. 10, p. 1099, doi. 10.1002/cmdc.200600133
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- Article
Drug Discovery Handbook. Edited by Shayne Cox Gad.
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- ChemMedChem, 2006, v. 1, n. 5, p. 572, doi. 10.1002/cmdc.200600021
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- Article
The Pipeline Is Filled...︁.
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- ChemMedChem, 2006, v. 1, n. 1, p. 3, doi. 10.1002/cmdc.200500072
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- Article
Synthesis and Structure-Activity Relationships of FAAH Inhibitors: Cyclohexylcarbamic Acid Biphenyl Esters with Chemical Modulation at the Proximal Phenyl Ring.
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- ChemMedChem, 2006, v. 1, n. 1, p. 130, doi. 10.1002/cmdc.200500017
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- Publication type:
- Article
Synthesis and Evaluation of 1,5-Benzodiazepines with Bridged Cycloalkyl Substituents at the N-1 Position as Potent and Selective CCK-B Ligands.
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- Archiv der Pharmazie, 1998, v. 331, n. 1, p. 41, doi. 10.1002/(SICI)1521-4184(199801)331:1<41::AID-ARDP41>3.0.CO;2-S
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- Article
Novel 1,5-Benzodiazepines as CCK-B Ligands. Effect of Aryl-Carbamic Substituents at the C-3 Position Together with Halogen Substitution on the Benzo-Fused Ring.
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- Archiv der Pharmazie, 1997, v. 330, n. 11, p. 353, doi. 10.1002/ardp.19973301107
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- Publication type:
- Article
An endocannabinoid mechanism for stress-induced analgesia.
- Published in:
- Nature, 2005, v. 435, n. 7045, p. 1108, doi. 10.1038/nature03658
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- Publication type:
- Article