Cannabinoid CB1 and orexin OX1 receptors have been suggested to form heterodimers and oligomers. Aimed at studying these complexes, a series of bivalent CB1 and OX1 ligands combining SR141716 and ACT-078573 pharmacophores were designed, synthesized, and tested for activity against CB1 and OX1 individually and in cell lines that coexpress both receptors. Compound <b>20</b> showed a robust enhancement in potency at both receptors when coexpressed as compared to individually expressed, suggesting possible interaction with CB1-OX1 dimers. Bivalent ligands targeting CB1-OX1 receptor dimers could be potentially useful as a tool for further exploring the roles of such heterodimers in vitro and in vivo
The objectives of this study were to identify the structural determinants for selective recognition ...
The CB1 cannabinoid receptor is a widely distributed G-protein coupled receptor in human central and...
ABSTRACT: Undesirable side effects associated with orthos-teric agonists/antagonists of cannabinoid ...
It has been proposed that OX1 orexin receptors and CB1 cannabinoid receptors can form heteromeric co...
Following inducible expression in HEK293 cells, the human orexin-1 receptor was targeted to the cell...
In order to obtain novel pharmacological tools and to investigate a multitargeting analgesic strateg...
The Endocannabinoid system (ECS) is a neuromodulator endogenous system. It consists of cannabinoid r...
In our ongoing program aimed at the design, synthesis, and biological evaluation of novel cannabinoi...
For centuries, man has exploited the Cannabis sativa plant for its therapeutic utility, primarily fo...
The potential, multifaceted therapeutic profile of cannabidiol (CBD), a major constituent derived fr...
The CB1 cannabinoid receptor, a member of the family A G-protein coupled receptors, is recognized as...
We investigated the pharmacology of three novel compounds, Org 27569 (5-chloro-3-ethyl-1H-indole-2-c...
Cannabis and cannabinoids are currently being investigated for their potential utility as therapeuti...
Novel 3-(1H-indol-3-yl)-1,2,4-oxadiazoles and -thiadiazoles were synthesized and found to be potent ...
Single chemical entities with potential to simultaneously interact with two binding sites are emergi...
The objectives of this study were to identify the structural determinants for selective recognition ...
The CB1 cannabinoid receptor is a widely distributed G-protein coupled receptor in human central and...
ABSTRACT: Undesirable side effects associated with orthos-teric agonists/antagonists of cannabinoid ...
It has been proposed that OX1 orexin receptors and CB1 cannabinoid receptors can form heteromeric co...
Following inducible expression in HEK293 cells, the human orexin-1 receptor was targeted to the cell...
In order to obtain novel pharmacological tools and to investigate a multitargeting analgesic strateg...
The Endocannabinoid system (ECS) is a neuromodulator endogenous system. It consists of cannabinoid r...
In our ongoing program aimed at the design, synthesis, and biological evaluation of novel cannabinoi...
For centuries, man has exploited the Cannabis sativa plant for its therapeutic utility, primarily fo...
The potential, multifaceted therapeutic profile of cannabidiol (CBD), a major constituent derived fr...
The CB1 cannabinoid receptor, a member of the family A G-protein coupled receptors, is recognized as...
We investigated the pharmacology of three novel compounds, Org 27569 (5-chloro-3-ethyl-1H-indole-2-c...
Cannabis and cannabinoids are currently being investigated for their potential utility as therapeuti...
Novel 3-(1H-indol-3-yl)-1,2,4-oxadiazoles and -thiadiazoles were synthesized and found to be potent ...
Single chemical entities with potential to simultaneously interact with two binding sites are emergi...
The objectives of this study were to identify the structural determinants for selective recognition ...
The CB1 cannabinoid receptor is a widely distributed G-protein coupled receptor in human central and...
ABSTRACT: Undesirable side effects associated with orthos-teric agonists/antagonists of cannabinoid ...