BAY-386 |
BAY-386 : Antagonist of F2R
Probe Summary
Selectivity
Potency
In Vivo
Control Compounds
Chemical Information
References
Vendors
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Probe Summary
| Targets | Biochemical/Biophysical Potency | Cellular Potency |
|---|---|---|
| F2R |
|
|
Antagonist
100 nM
Selectivity
In Vitro Selectivity Assessment
Selectivity Assessment Description:
Selectivity within target family: F2RL3 (PAR4): Functional cellular assay (HEK cells) IC50 > 10 µM ( ...
Potency Cellular
In Vitro
F2R
Mode of Action: Antagonist
Structure-Activity-Relationship data available? Yes
DOI Reference: 10.7554/eLife.34311
In Vivo Validations
Negative Control Compounds
BAY-448
Notes: Functional cellular assays (HEK cells): > 1,000 times less active on F2R (IC50 >10 µM) and F2RL3 (IC50 >> 5 µM); Binding assay (platelet membranes): IC50 > 10 µM); Eurofins-Cerep cellular and nuclear receptor functional assay screen (25) at 10 µM: clean; Clean GPCR scan
Chemical Information
| Molecular Formula | C22H25F3N4O5S |
| SMILEs | O=C(N1CCS(=O)(=O)CC1)N1C[C@H](c2ccc(OC(F)(F)F)cc2)C[C@H](c2nc(C3CC3)no2)C1 |
| InChI | InChI=1S/C22H25F3N4O5S/c23-22(24,25)33-18-5-3-14(4-6-18)16-11-17(20-26-19(27-34-20)15-1-2-15)13-29(12-16)21(30)28-7-9-35(31,32)10-8-28/h3-6,15-17H,1-2,7-13H2/t16-,17+/m1/s1 |
| Molecular weight | 514.15 Da |
| AlogP | 0.0 |
| HBond acceptors | 9 |
| HBond donors | -- |
| Atoms | 60 |