ω-Imidazolyl- and ω-Tetrazolylalkylcarbamates as Inhibitors of Fatty Acid Amide Hydrolase: Biological Activity and in vitro Metabolic Stability-Reference-Cited by-同舟云学术

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ω-Imidazolyl- and ω-Tetrazolylalkylcarbamates as Inhibitors of Fatty Acid Amide Hydrolase: Biological Activity and in vitro Metabolic Stability

Published:2016-01-06 Issue:4 Volume:11 Page:429-443
ISSN:1860-7179
Container-title:ChemMedChem
language:en
Short-container-title:ChemMedChem

Author:

Terwege Tobias¹,Hanekamp Walburga¹,Garzinsky David¹,König Simone²,Koch Oliver³,Lehr Matthias¹

Affiliation:

1. Institute of Pharmaceutical and Medicinal Chemistry; University of Münster; Corrensstrasse 48 48149 Münster Germany

2. Core Unit Proteomics; Interdisciplinary Center for Clinical Research (IZKF); University of Münster; Röntgenstrasse 21 48149 Münster Germany

3. Faculty of Chemistry and Chemical Biology; TU Dortmund University; Otto-Hahn-Strasse 6 44227 Dortmund Germany

Funder

Bundesministerium für Bildung und Forschung (BMBF)

Publisher

Wiley

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics,Molecular Medicine,Drug Discovery,Biochemistry,Pharmacology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/cmdc.201500445/fullpdf

Reference55 articles.

1. The cannabinoid system and its pharmacological manipulation ? a review, with emphasis upon the uptake and hydrolysis of anandamide

2. Endocannabinoids: synthesis and degradation

3. International Union of Pharmacology. XXVII. Classification of Cannabinoid Receptors

4. CB1 and CB2 receptor-mediated signalling: a focus on endocannabinoids

5. Cannabinoid Receptors: A brief history and "what's hot".

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