JH-X-119-01 |
JH-X-119-01 : Covalent inhibitor of IRAK1 and YSK4
Probe Summary
Selectivity
Potency
In Vivo
Control Compounds
Chemical Information
References
Vendors
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Probe Summary
| Targets | Biochemical/Biophysical Potency | Cellular Potency |
|---|---|---|
| IRAK1 |
|
Covalent
1-10 µM
Selectivity
In Vitro Selectivity Assessment
MAP3K19
Gene ID: Q56UN5
Organism: Homo sapiens
Family: STE Ser/Thr protein kinase family
Potency: IC50 - 57 nM
Potency Assay Off-Target:
JH-X-119-01 showed exceptional kinome selectivity, as measured by a KINOMEScan selectivity score of ...
Potency Cellular
In Vitro
IRAK1
Mode of Action: Covalent
Structure-Activity-Relationship data available? Yes
DOI Reference: 10.1021/acsmedchemlett.0c00378
In Vivo Validations
Mouse
Dose: 5 mg/kg
Route of delivery:
Intravenous
Plasma half life:
2.24 h
Systemic clearance:
18.8 ml/min/Kg
Cmax:
Cmax = 9.95 µM
Volume of Distribution at Steady-State:
Vss=0.46 L/Kg
DOI Reference: 10.1021/acsmedchemlett.0c00378
Chemical Information
| Molecular Formula | C25H20N6O3 |
| SMILEs | C=CC(=O)Nc1cccc(C(=O)Nc2ccc(NC(=O)c3cccc(-c4ccn[nH]4)n3)cc2)c1 |
| InChI | InChI=1S/C25H20N6O3/c1-2-23(32)27-19-6-3-5-16(15-19)24(33)28-17-9-11-18(12-10-17)29-25(34)22-8-4-7-20(30-22)21-13-14-26-31-21/h2-15H,1H2,(H,26,31)(H,27,32)(H,28,33)(H,29,34) |
| Molecular weight | 452.16 Da |
| AlogP | 0.0 |
| HBond acceptors | 9 |
| HBond donors | 4 |
| Atoms | 54 |
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