GPR55 Receptor Agonists: Small Molecules and Peptides
Members of the G protein-coupled receptor (GPCR) family, such as GPR55, play important roles in signal transduction from the external environment to the inside of the cell. GPR55 is a receptor for L-alpha-lysophosphatidylinositol (LPI). LPI induces Ca2+ release from intracellular stores via the heterotrimeric G protein GNA13 and RHOA. GPR55 is expressed in the caudate nucleus and putamen, but not detected in the hippocampus, thalamus, pons cerebellum, frontal cortex of the brain or in the liver. It is expressed in osteoclasts and osteoblasts. GPR55 may play a role in bone physiology by regulating osteoclast number and function. GPR55 may also be involved in hyperalgesia associated with inflammatory and neuropathic pain.
5 results for "GPR55 Receptor Agonists Small Molecules and Peptides" in Products
5 results for "GPR55 Receptor Agonists Small Molecules and Peptides" in Products
GPR55 Receptor Agonists: Small Molecules and Peptides
Members of the G protein-coupled receptor (GPCR) family, such as GPR55, play important roles in signal transduction from the external environment to the inside of the cell. GPR55 is a receptor for L-alpha-lysophosphatidylinositol (LPI). LPI induces Ca2+ release from intracellular stores via the heterotrimeric G protein GNA13 and RHOA. GPR55 is expressed in the caudate nucleus and putamen, but not detected in the hippocampus, thalamus, pons cerebellum, frontal cortex of the brain or in the liver. It is expressed in osteoclasts and osteoblasts. GPR55 may play a role in bone physiology by regulating osteoclast number and function. GPR55 may also be involved in hyperalgesia associated with inflammatory and neuropathic pain.
Potent CB1 antagonist; also GPR55 agonist
| Chemical Name: | N-(Piperidin-1-yl)-5-(4-iodophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide |
| Purity: | ≥99% (HPLC) |
Selective GPR55 agonist. FAAH and PAA substrate
| Alternate Names: | PEA |
| Chemical Name: | N-(2-Hydroxyethyl)hexadecanamide |
Lipid mediator, anorexic actions; also GPR55 and PPARα agonist
| Chemical Name: | (9Z)-N-(2-Hydroxyethyl)-9-octadecenamide |
| Purity: | ≥99% |
Potent GPR55 agonist
| Chemical Name: | 5-Methyl-4-[(1R,6R)-3-methyl-6-(1-methylethenyl)-2-cyclohexen-1-yl]-1,3-benzenediol |
| Purity: | ≥97% (HPLC) |
Selective GPR55 agonist; also promotes NSC proliferation and differentiation
| Chemical Name: | 3-[[4-(2,3-Dimethylphenyl)-1-piperazinyl]carbonyl]-N,N-dimethyl-4-(1-pyrrolidinyl)benzenesulfonamide |
| Purity: | ≥98% |
