JNJ-6204 |
JNJ-6204 : Inhibitor of CSNK1D, CSNK1E
Probe Summary
Selectivity
Potency
In Vivo
Control Compounds
Chemical Information
References
Vendors
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Probe Summary
| Targets | Biochemical/Biophysical Potency | Cellular Potency |
|---|---|---|
| CSNK1D |
|
|
| CSNK1E |
|
Inhibitor
up to 10µM
up to 1 uM
Selectivity
In Vitro Selectivity Assessment
Potency Assay Off-Target:
Closely related kinases: CSNK1A1 (IC50 = 419 nM)
Panel of 370 kinases at 1 μM: clean; Closest hit: T ...
Potency Cellular
In Vitro
CSNK1D
Mode of Action: Inhibitor
Structure-Activity-Relationship data available? Yes
DOI Reference: 10.1021/acsmedchemlett.3c00523
CSNK1E
Mode of Action: Inhibitor
Structure-Activity-Relationship data available? Yes
DOI Reference: 10.1021/acsmedchemlett.3c00523
In Vivo Validations
Mouse
Dose: 1 mg/Kg IV, 5 mg/Kg PO
Route of delivery:
Intravenous, Oral
Systemic clearance:
33 mL/min/Kg
Cmax:
1250 ng/mL
Area Under the Curve::
113 h*ng/mL
Bioavailability:
43%
DOI Reference: 10.1021/acsmedchemlett.3c00523
Negative Control Compounds
CANSAR3893768
Notes: JNJ-0293: Purified Enzyme, ADP-GLO: IC50 = 6.9 μM; BRET whole cell binding assay: IC50 > 10 μM
Chemical Information
| Molecular Formula | C19H17FN6O |
| InChI | InChI=1S/C19H17FN6O/c1-19(2)10-26-15(9-27-19)16(12-5-6-21-18-13(12)8-23-24-18)17(25-26)14-4-3-11(20)7-22-14/h3-8H,9-10H2,1-2H3,(H,21,23,24) |
| Molecular weight | 364.14 Da |
| AlogP | 0.0 |
| HBond acceptors | 7 |
| HBond donors | 1 |
| Atoms | 44 |