GPR120-IN-1 |
Agonist of FFAR4
Probe Summary
Selectivity
Potency
In Vivo
Control Compounds
Chemical Information
References
Vendors
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Probe Summary
| Targets | Biochemical/Biophysical Potency | Cellular Potency |
|---|---|---|
| FFAR4 |
|
Agonist
up to 10 uM
Selectivity
In Cell Selectivity Assessment
Selectivity Assessment Description:
No activity detected on FFAR1 in both human and mouse variants.
Potency Cellular
In Vitro
FFAR4
Mode of Action: Agonist
Structure-Activity-Relationship data available? No
In Vivo Validations
Mouse
Dose: 30 mg/Kg
Reference: --
Orthogonal Probes def
TUG-891
Chemical Information
| Molecular Formula | C19H23ClF3NO3 |
| SMILEs | O=C(O)CC1CCC2(CC1)CCN(c1cc(OC(F)(F)F)ccc1Cl)CC2 |
| InChI | InChI=1S/C19H23ClF3NO3/c20-15-2-1-14(27-19(21,22)23)12-16(15)24-9-7-18(8-10-24)5-3-13(4-6-18)11-17(25)26/h1-2,12-13H,3-11H2,(H,25,26) |
| Molecular weight | 405.13 Da |
| AlogP | 5.490100000000004 |
| HBond acceptors | 4 |
| HBond donors | 1 |
| Atoms | 50 |
References
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