| Literature DB >> 34161090 |
Gemma Navarro1,2, Angel Gonzalez3, Adrià Sánchez-Morales4, Nil Casajuana-Martin3, Marc Gómez-Ventura4, Arnau Cordomí3, Félix Busqué4, Ramon Alibés4, Leonardo Pardo3, Rafael Franco2,5.
Abstract
Cannabidiol (CBD), the second most abundant of the active compounds found in the Cannabis sativa plant, is of increasing interest because it is approved for human use and is neither euphorizing nor addictive. Here, we design and synthesize novel compounds taking into account that CBD is both a partial agonist, when it binds to the orthosteric site, and a negative allosteric modulator, when it binds to the allosteric site of the cannabinoid CB2 receptor. Molecular dynamic simulations and site-directed mutagenesis studies have identified the allosteric site near the receptor entrance. This knowledge has permitted to perform structure-guided design of negative and positive allosteric modulators of the CB2 receptor with potential therapeutic utility.Entities:
Year: 2021 PMID: 34161090 DOI: 10.1021/acs.jmedchem.1c00561
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446