| Name | CID 16020046 |
| Description | CID 16020046 (C390-0219) is a selective GPR55 antagonist, inhibiting GPR55 constitutive activity with IC50 of 0.15 μM in yeast. |
| In vitro | In yeast cells expressing human GPR55, CID16020046 inhibited agonist-induced receptor activation. In human embryonic kidney (HEK293) cells stably expressing human GPR55, CID16020046 behaved as an antagonist on LPI-mediated Ca2+ release and extracellular signal-regulated kinases activation, but not in HEK293 cells expressing cannabinoid receptor 1 or 2 (CB1 or CB2). CID16020046 dose-dependently inhibited lysophosphatidylinositol (LPI)-induced activation of nuclear factor of activated T-cells (NFAT), nuclear factor κ of activated B cells (NF-κB) and serum response element, translocation of NFAT and NF-κB, and GPR55 internalization [1]. |
| Storage | Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | 10% DMSO+40% PEG300+5% Tween 80+45% Saline : 2 mg/mL (4.7 mM), Sonication is recommended. DMSO : 55 mg/mL (129.28 mM), Sonication is recommended.
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| Keywords | wound | platelet | phosphorylation | m-opioid | lysophosphatidylinositol | LPI | KCNH2 | Inhibitor | inhibit | HMVEC | hERG | HEK | healing | GPR55 | G protein-coupled receptor 55 | function | ERK1/2 | endothelial | CID-16020046 | CID16020046 | CID 16020046 | cells | CannabinoidReceptor | Cannabinoid Receptor | Ca2+ | acetylcholinesterase |
| Inhibitors Related | RTICBM-189 | β-Caryophyllene | CB2 modulator 1 | Pregnenolone | Pregnenolone acetate | CB1 antagonist 2 | Dehydroabiethylamine | CB2 receptor agonist 2 | AM-1235 | 2,3-Butanediol | Drinabant | AM281 |
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