Literature DB >> 20015447

High-performance liquid chromatography assay with fluorescence detection for the evaluation of inhibitors against human recombinant monoacylglycerol lipase.

Angela Holtfrerich1, Teona Makharadze, Matthias Lehr.   

Abstract

A fluorescent assay for the evaluation of inhibitors of monoacylglycerol lipase (MAGL) is described. 1,3-Dihydroxypropan-2-yl 4-pyren-1-ylbutanoate was designed and synthesized as novel fluorogenic substrate. Activity of human recombinant MAGL was determined in the presence of the surfactant Triton X-100 without further sample cleanup by measuring the amount of 4-pyren-1-ylbutanoic acid released by the enzyme with reversed-phase high-performance liquid chromatography (HPLC) and fluorescence detection. The known covalent binding MAGL inhibitors methyl arachidonyl fluorophosphonate (MAFP), 4-nitrophenyl 4-[bis(1,3-benzodioxol-5-yl)hydroxymethyl]piperidine-1-carboxylate (JZL184), and [4-(5-methoxy-2-oxo-1,3,4-oxadiazol-3-yl)-2-methylphenyl]carbamic acid benzyl ester (CAY10499) were used to validate the test system. Applying an incubation time of 15 min, the IC(50) values obtained for these compounds were 0.16, 3.7, and 1.1 microM, respectively. A prolongation of the incubation to 45 min results in a two- to threefold decrease of the IC(50) values. Copyright 2010 Elsevier Inc. All rights reserved.

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Year:  2009        PMID: 20015447     DOI: 10.1016/j.ab.2009.12.015

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  6 in total

1.  Magnolia Extract, Magnolol, and Metabolites: Activation of Cannabinoid CB2 Receptors and Blockade of the Related GPR55.

Authors:  Viktor Rempel; Alexander Fuchs; Sonja Hinz; Tadeusz Karcz; Matthias Lehr; Uwe Koetter; Christa E Müller
Journal:  ACS Med Chem Lett       Date:  2012-11-14       Impact factor: 4.345

2.  Identification by nuclear magnetic resonance spectroscopy of an active-site hydrogen-bond network in human monoacylglycerol lipase (hMGL): implications for hMGL dynamics, pharmacological inhibition, and catalytic mechanism.

Authors:  Ioannis Karageorgos; Sergiy Tyukhtenko; Nikolai Zvonok; David R Janero; Christine Sallum; Alexandros Makriyannis
Journal:  Mol Biosyst       Date:  2010-05-12

3.  (Indolylalkyl)piperidine carbamates as inhibitors of fatty acid amide hydrolase (FAAH).

Authors:  Helmut Dahlhaus; Walburga Hanekamp; Matthias Lehr
Journal:  Medchemcomm       Date:  2017-01-30       Impact factor: 3.597

4.  Aryl N-[ω-(6-Fluoroindol-1-yl)alkyl]carbamates as Inhibitors of Fatty Acid Amide Hydrolase, Monoacylglycerol Lipase, and Butyrylcholinesterase: Structure-Activity Relationships and Hydrolytic Stability.

Authors:  Stefan Rudolph; Helmut Dahlhaus; Walburga Hanekamp; Christian Albers; Maximilian Barth; Giulia Michels; Denise Friedrich; Matthias Lehr
Journal:  ACS Omega       Date:  2021-05-14

5.  Hexafluoroisopropyl Carbamates as Selective MAGL and Dual MAGL/FAAH Inhibitors: Biochemical and Physicochemical Properties.

Authors:  Maximilian Barth; Stefan Rudolph; Jan Kampschulze; Imke Meyer Zu Vilsendorf; Walburga Hanekamp; Dennis Mulac; Klaus Langer; Matthias Lehr
Journal:  ChemMedChem       Date:  2022-02-18       Impact factor: 3.540

Review 6.  Inhibitors of Fatty Acid Amide Hydrolase and Monoacylglycerol Lipase: New Targets for Future Antidepressants.

Authors:  Shintaro Ogawa; Hiroshi Kunugi
Journal:  Curr Neuropharmacol       Date:  2015       Impact factor: 7.363

  6 in total

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