Compound Detail
CHEMBL5403572
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[2H]C([2H])([2H])NC(=O)c1nnc(Nc2ccccn2)cc1Nc1nccc(-c2ncc(F)cn2)c1OC
Basic Information
| ChEMBL ID | CHEMBL5403572 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | JHYMZJKRDFVXDT-FIBGUPNXSA-N |
| Parent Compound | CHEMBL5498932 |
| Active Moiety | CHEMBL5498932 |
1
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names
Molecular Properties
447.4
MW (Da)
2.72
ALogP
10
HBA
3
HBD
139.7
PSA (Ų)
0.39
QED
0
Ro5 Violations
7
Rot. Bonds
Drug Information
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 2 meas. best 9.7
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Non-receptor tyrosine-protein kinase TYK2 CHEMBL3553 | IC50 | 9.7 | 8.085 | 0.2 | 2 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Non-receptor tyrosine-protein kinase TYK2 | IC50 | = | 0.2 | nM | 9.7 | Displacement of fluorescein-labeled kinase tracer from His-TVMV-TYK2 JH2 (575 to... | 37315697 |
| Non-receptor tyrosine-protein kinase TYK2 | IC50 | = | 339.0 | nM | 6.47 | Inhibition of TYK2 JH2 domain in human whole blood assessed as reduction in IFNa... | 37315697 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 37315697 | 10.1016/j.bmcl.2023.129373 | ADMET | 3 |
| 37315697 | 10.1016/j.bmcl.2023.129373 | Non-receptor tyrosine-protein kinase TYK2 | 2 |
Data from ChEMBL 36 via Core Engine