Tandem mass spectrometric data-FAAH inhibitory activity relationships of some carbamic acidO-aryl esters
Open Access
- 3 December 2004
- journal article
- research article
- Published by Wiley in Journal of Mass Spectrometry
- Vol. 39 (12), 1450-1455
- https://doi.org/10.1002/jms.729
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- The molecular logic of endocannabinoid signallingNature Reviews Neuroscience, 2003
- Evidence for Distinct Roles in Catalysis for Residues of the Serine-Serine-Lysine Catalytic Triad of Fatty Acid Amide HydrolaseJournal of Biological Chemistry, 2003
- Design, Synthesis, and Structure−Activity Relationships of Alkylcarbamic Acid Aryl Esters, a New Class of Fatty Acid Amide Hydrolase InhibitorsJournal of Medicinal Chemistry, 2003
- Modulation of anxiety through blockade of anandamide hydrolysisNature Medicine, 2002
- Electrochemical processes in electrospray ionization mass spectrometryJournal of Mass Spectrometry, 2000
- Chemical and Mutagenic Investigations of Fatty Acid Amide Hydrolase: Evidence for a Family of Serine Hydrolases with Distinct Catalytic PropertiesBiochemistry, 1999
- Correlation of the antimetastatic properties of aryltriazenes with their electron impact ionization mass spectrometryRapid Communications in Mass Spectrometry, 1997
- Letter to the Editor: Correlation of the mutagenic properties of aryl- and heteroaryltriazenes with their electron ionization induced fragmentationRapid Communications in Mass Spectrometry, 1996
- 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 agentsJournal of Mass Spectrometry, 1995
- Isolation and Structure of a Brain Constituent That Binds to the Cannabinoid ReceptorScience, 1992