Loratadine analogues as MAGL inhibitors-Reference-Cited by-同舟云学术

Loratadine analogues as MAGL inhibitors

Published:2015-04 Issue:7 Volume:25 Page:1436-1442
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Patel Jayendra Z.,Ahenkorah Stephen,Vaara Miia,Staszewski Marek,Adams Yahaya,Laitinen Tuomo,Navia-Paldanius Dina,Parkkari Teija,Savinainen Juha R.,Walczyński Krzysztof,Laitinen Jarmo T.,Nevalainen Tapio J.

Funder

Graduate School of Drug Design, UEF

The Academy of Finland

Biocenter Finland/DDCB

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference49 articles.

1. Brain monoglyceride lipase participating in endocannabinoid inactivation

2. Identification of an endogenous 2-monoglyceride, present in canine gut, that binds to cannabinoid receptors

3. 2-Arachidonoylgylcerol: A Possible Endogenous Cannabinoid Receptor Ligand in Brain

4. A Comprehensive Profile of Brain Enzymes that Hydrolyze the Endocannabinoid 2-Arachidonoylglycerol

5. The serine hydrolases MAGL, ABHD6 and ABHD12 as guardians of 2-arachidonoylglycerol signalling through cannabinoid receptors

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