FAAH-Catalyzed C–C Bond Cleavage of a New Multitarget Analgesic Drug

Autor: David F. Woodward, Marco Allarà, Fabiana Piscitelli, Francesca Guida, Angela Amoresano, Jenny W. Wang, Livio Luongo, Rosa Maria Vitale, Cristoforo Silvestri, Vincenzo Di Marzo, Anna Illiano, Alessia Ligresti, Jose L. Martos, Pietro Amodeo, Gennaro Marino, Robert W. Carling, Sabatino Maione

Publikováno v: ACS chemical neuroscience (2018). doi:10.1021/acschemneuro.8b00315
info:cnr-pdr/source/autori:Ligresti A.; Silvestri C.; Vitale R.M.; Martos J.L.; Piscitelli F.; Wang J.W.; Allara M.; Carling R.W.; Luongo L.; Guida F.; Illiano A.; Amoresano A.; Maione S.; Amodeo P.; Woodward D.F.; Di Marzo V.; Marino G./titolo:FAAH-Catalyzed C-C Bond Cleavage of a New Multitarget Analgesic Drug/doi:10.1021%2Facschemneuro.8b00315/rivista:ACS chemical neuroscience/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume

The discovery of extended catalytic versatilities is of great importance in both the chemistry and biotechnology fields. Fatty acid amide hydrolase (FAAH) belongs to the amidase signature superfamily and is a major endocannabinoid inactivating enzyme

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f3c3742f4f0d43e9590930ffd994e96
https://doi.org/10.1021/acschemneuro.8b00315