JP3000 |
JP3000 : Agonist of RXRA, RXRB, RXRG
Probe Summary
Selectivity
Potency
In Vivo
Control Compounds
Chemical Information
References
Vendors
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Probe Summary
| Targets | Biochemical/Biophysical Potency | Cellular Potency |
|---|---|---|
| RXRA |
|
|
| RXRB |
| |
| RXRG |
|
Agonist
between 100 nM and 1 uM
Selectivity
In Vitro Selectivity Assessment
Potency Assay Off-Target:
Tested on 27 related nuclear receptors at 1 µM (in-house panel): clean (> 100 fold selectivity)
Potency Cellular
In Vitro
RXRA
Mode of Action: Agonist
Structure-Activity-Relationship data available? Yes
Other Reference: Peer reviewed at SGC
RXRB
Mode of Action: Agonist
Structure-Activity-Relationship data available? Yes
Other Reference: Peer reviewed at SGC
RXRG
Mode of Action: Agonist
Structure-Activity-Relationship data available? No
Other Reference: Peer reviewed at SGC
Negative Control Compounds
JP3001
Notes: EC50 (RXRα/β/γ): all > 10 µM (hybrid reporter gene assays)
PubChem ID:
Chemical Information
| Molecular Formula | C21H13F6NO3 |
| SMILEs | O=C(O)C1CC1c1nc(-c2ccccc2)c(-c2cc(C(F)(F)F)cc(C(F)(F)F)c2)o1 |
| InChI | InChI=1S/C21H13F6NO3/c22-20(23,24)12-6-11(7-13(8-12)21(25,26)27)17-16(10-4-2-1-3-5-10)28-18(31-17)14-9-15(14)19(29)30/h1-8,14-15H,9H2,(H,29,30) |
| Molecular weight | 441.08 Da |
| AlogP | 0.0 |
| HBond acceptors | 4 |
| HBond donors | 1 |
| Atoms | 44 |
References
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