Heteroaryl urea inhibitors of fatty acid amide hydrolase: Structure–mutagenicity relationships for arylamine metabolites-Reference-Cited by-同舟云学术

Heteroaryl urea inhibitors of fatty acid amide hydrolase: Structure–mutagenicity relationships for arylamine metabolites

Published:2012-12 Issue:24 Volume:22 Page:7357-7362
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Tichenor Mark S.,Keith John M.,Jones William M.,Pierce Joan M.,Merit Jeff,Hawryluk Natalie,Seierstad Mark,Palmer James A.,Webb Michael,Karbarz Mark J.,Wilson Sandy J.,Wennerholm Michelle L.,Woestenborghs Filip,Beerens Dominiek,Luo Lin,Brown Sean M.,Boeck Marlies De,Chaplan Sandra R.,Breitenbucher J. Guy

Publisher

Elsevier BV

Subject

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

Reference57 articles.

1. STRUCTURE AND FUNCTION OF FATTY ACID AMIDE HYDROLASE

2. Supersensitivity to anandamide and enhanced endogenous cannabinoid signaling in mice lacking fatty acid amide hydrolase

3. Fatty acid amide hydrolase as a potential therapeutic target for the treatment of pain and CNS disorders

4. Discovery and Development of Fatty Acid Amide Hydrolase (FAAH) Inhibitors

5. Covalent Inhibitors of Fatty Acid Amide Hydrolase: A Rationale for the Activity of Piperidine and Piperazine Aryl Ureas

Cited by 19 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. 2,1,3-Benzothiadiazoles Are Versatile Fluorophore Building Blocks for the Design of Analyte-Sensing Optical Devices;Chemosensors;2024-08-07

2. Mild and efficient synthesis and base-promoted rearrangement of novel isoxazolo[4,5-b]pyridines;Beilstein Journal of Organic Chemistry;2024-05-14

3. Accessing three-dimensional molecular diversity through benzylic C–H cross-coupling;Nature Synthesis;2023-06-01

4. Synthesis of isoxazolo[4,5-b]pyridine derivatives (microreview);Chemistry of Heterocyclic Compounds;2023-05

5. From Synthetic Simplified Marine Metabolite Analogues to New Selective Allosteric Inhibitor of Aurora B Kinase;Journal of Medicinal Chemistry;2021-01-08