JNJ-47117096 |
JNJ-47117096 : Inhibitor of MELK
Probe Summary
Selectivity
Potency
In Vivo
Control Compounds
Chemical Information
References
Vendors
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Probe Summary
| Targets | Biochemical/Biophysical Potency | Cellular Potency |
|---|---|---|
| MELK |
|
|
Inhibitor
higher concentrations of up to 5 µM or 10 µM
1 µM
Selectivity
In Vitro Selectivity Assessment
FLT3
Gene ID: P36888
Organism: Homo sapiens
Family: Tyr protein kinase family
Potency: IC50 - 18 nM
Potency Assay Off-Target:
Radioactive filter binding assay (10 µM ATP)
Selectivity Assessment Description:
Screened at 1 µM against 235 kinases, KinaseProfile service (Millipore). Closest targets as % of con ...
In Cell Selectivity Assessment
Potency Assay Off-Target:
inhibition of proliferation with IC50 1.5 μM in the absence of IL-3 in Ba/F3-Flt3 cells but no inh ...
Potency Cellular
In Vitro
MELK
Mode of Action: Inhibitor
Structure-Activity-Relationship data available? Yes
DOI Reference: 10.1021/ml5001245
Orthogonal Probes def
NVS-MELK8a
ChEMBL ID:
CHEMBL3824068
Chemical Information
| Molecular Formula | C21H22N4O2 |
| SMILEs | COc1cc(-c2cn[nH]c2)ccc1C(=O)Nc1ccc2c(c1)CCNCC2 |
| InChI | InChI=1S/C21H22N4O2/c1-27-20-11-15(17-12-23-24-13-17)3-5-19(20)21(26)25-18-4-2-14-6-8-22-9-7-16(14)10-18/h2-5,10-13,22H,6-9H2,1H3,(H,23,24)(H,25,26) |
| Molecular weight | 362.17 Da |
| AlogP | 3.025800000000001 |
| HBond acceptors | 6 |
| HBond donors | 3 |
| Atoms | 49 |