نتایج جستجو برای: acid amide hydrolase

تعداد نتایج: 772887  

Journal: :Journal of Cerebral Blood Flow & Metabolism 2012

2007
Kazuhiro Ito Gaetano Caramori Ian M. Adcock Jun Nagai Mamoru Kurokawa Hiroshi Takeshima Brigitte L. Kieffer Jun-Xu Li Ginger L. Becker John R. Traynor Gianluigi Tanda Aaron L. Ebbs Theresa A. Kopajtic Lyn M. Elias Bettye L. Campbell Amy H. Newman Tadanobu Utsuki Nao Uchimura Mitsuru Irikura Hiroshi Moriuchi Harold W. Holloway Qian-Sheng Yu Edward L. Spangler Jacek Mamczarz Donald K. Ingram Tetsumi Irie Nigel H. Greig Marcello Solinas Zuzana Justinova Carrie E. Wertheim Sevil Yasar Daniele Piomelli Subramanian K. Vadivel Alexandros Makriyannis Kumkum Ganguly Juan-Carlos Murciano Randal Westrick John Leferovich Douglas B. Cines Vladimir R. Muzykantov Volodymyr Labinskyy Michelle Bellomo Margaret P. Chandler Martin E. Young Vincenzo Lionetti Khaled Qanud Federico Bigazzi Tiziana Sampietro William C. Stanley Fabio A. Recchia

The Endogenous Cannabinoid Anandamide Produces -9Tetrahydrocannabinol-Like Discriminative and Neurochemical Effects That Are Enhanced by Inhibition of Fatty Acid Amide Hydrolase but Not by Inhibition of Anandamide Transport Marcello Solinas, Gianluigi Tanda, Zuzana Justinova, Carrie E. Wertheim, Sevil Yasar, Daniele Piomelli, Subramanian K. Vadivel, Alexandros Makriyannis, and Steven R. Goldber...

Journal: :Chemical communications 2014
Alessio De Simone Gian Filippo Ruda Clara Albani Glauco Tarozzo Tiziano Bandiera Daniele Piomelli Andrea Cavalli Giovanni Bottegoni

Combining computer-assisted drug design and synthetic efforts, we generated compounds with potent and balanced activities toward both D3 dopamine receptor and fatty acid amide hydrolase (FAAH) enzyme. By concurrently modulating these targets, our compounds hold great potential toward exerting a disease-modifying effect on nicotine addiction and other forms of compulsive behavior.

Journal: :The Journal of biological chemistry 2006
Binqing Q Wei Tarjei S Mikkelsen Michele K McKinney Eric S Lander Benjamin F Cravatt

Fatty acid amides constitute a large and diverse class of lipid transmitters that includes the endogenous cannabinoid anandamide and the sleep-inducing substance oleamide. The magnitude and duration of fatty acid amide signaling are controlled by enzymatic hydrolysis in vivo. Fatty acid amide hydrolase (FAAH) activity in mammals has been primarily attributed to a single integral membrane enzyme...

Journal: :Chemistry & biology 2005
Dale G Deutsch

In this issue of Chemistry & Biology, Alexander and Cravatt propose a model for the binding of carbamate inhibitors to fatty acid amide hydrolase (FAAH), the enzyme that breaks down signaling lipids. Using competitive activity-based protein profiling and click chemistry, they designed potent and selective FAAH inhibitors and characterized their off-target reactions.

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