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GPBAR1 agonist
In Stock
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| Cell Line | Activity | Value | Description | Reference |
|---|---|---|---|---|
| HEK293 | EC50 | 1.03 μM | Agonist activity at GP-BAR1 (unknown origin) in human HEK293 cells assessed as receptor transactivation at 100 nM to 50 uM incubated for 16 hrs by CRE-driven luciferase reporter gene assay | [PMID: 25247751] |
| Manufacturer | Adooq Bioscience |
|---|---|
| Actions | Agonist |
| CAS Number | 1632118-69-4 |
| Applications | GPBAR1 agonist |
| Formula | C26H46O3 |
| Molecular Weight | 406.64 |
| SMILES | C[C@H](CCCO)[C@@]1([H])CC[C@@]2([H])[C@]3([H])[C@@H](O)[C@@H](CC)[C@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])CC[C@@]21C |
| Solvent | Reported Solubility |
|---|---|
| DMSO | 79 mg/mL (194.27 mM) |
| Water | Insoluble |
| Ethanol | 79 mg/mL |
| Concentration | |
|---|---|
Values use four significant digits. Prepare to the final solution volume; this is not the volume of solvent to add.
Stock preparation is unavailable for this product molecular weight.
Calculated stock concentrations do not establish solvent solubility. Refer to the reported solubility data for experimental guidance.
Store powder at -20°C, keep desiccated.
In powder form, the chemical is stable for 36 months.
In solution, store at -20°C and use within 1 month to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.
