Related Experiment Video
Updated: Jun 5, 2026

Methods for the Discovery of Novel Compounds Modulating a Gamma-Aminobutyric Acid Receptor Type A Neurotransmission
Published on: August 16, 2018
Benzamide derivatives as allosteric ligands of the human and rat P2X7 receptor
Andrea Spinaci1, Aleksei Smirnov1, Beatrice Francucci1
1School of Pharmacy, Medicinal Chemistry Unit, University of Camerino, Via Madonna Delle Carceri, 62032, Camerino, Italy.
Abstract:
The P2X7 receptor (P2X7R) is a key player of the purinergic signalling and is widely expressed throughout the body. The involvement of this protein in the regulation of physiological processes and the onset and progression of pathological conditions make the P2X7R a key target for the development of novel pharmacological tools for the treatment of inflammation-related conditions, cancer, and neurological diseases. Here we report the synthesis and biological evaluation of an array of 2-bromo-benzamide derivatives as novel allosteric ligands of the P2X7R. The compounds ability to bind and inhibit the receptor was evaluated with radioligand binding assay at both the human and rat proteins and functional studies at the human P2X7R, stably transfected in HEK293 cells. The affinity was analysed with the aid of molecular modelling studies performed at both receptors. All the compounds showed nanomolar to micromolar affinity for the human P2X7R and a lower ability to bind the rat protein. Inhibitory potency at the human P2X7R ranged from nanomolar to micromolar levels, with one compound showing sub-nanomolar inhibitory potency. These results confirm the 2-bromo-benzamide scaffold as a solid basis for the development of novel P2X7R allosteric ligands.
Related Concept Videos
Ligand-Gated Ion Channel Receptor: Gating Mechanism
Ligand-gated Ion Channels
Three Subfamilies of Ligand-gated Ion Channels
Ligand-gated ion channels fall into three subfamilies. The 'Cys-loop' includes the nicotinic acetylcholine receptors, γ-aminobutyric acid (GABA), glycine, and 5-hydroxytryptamine receptors. The second one is the 'Pore-loop' channels that include the...
Adrenergic Antagonists: Chemistry and Classification of ɑ-Receptor Blockers
Nonselective α-blockers: Nonselective α-blockers contain haloalkylamine or imidazoline moieties. Phenoxybenzamine, with a haloalkylamine...
Adrenergic Agonists: Chemistry and Structure-Activity Relationship
Aromatic ring substitutions: Substituting the aromatic ring with –OH groups at positions 3 and 4 yields catecholamines (e.g., epinephrine), which have a high affinity for adrenoceptors. Hydrogen bonding between –OH groups and receptors enhances adrenergic activity.
Separation of the aromatic...
Drug-Receptor Interaction: Agonist
Agonists can bind to receptors in different ways. Some agonists bind directly to the receptor's active site, mimicking the endogenous ligand's action.
Ligand Binding and Linkage
