Compound Detail
CHEMBL4293510
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NC(=O)c1cnc2c(N[C@H]3C[C@H]3F)cc(Nc3cccc(-c4ccc(C(F)(F)F)cc4F)c3)nn12
Basic Information
| ChEMBL ID | CHEMBL4293510 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | UMHAGOZMLWBAGB-SJORKVTESA-N |
1
Targets
3
Activities
1
Assay Types
3
PK Parameters
3
Publications
0
Known Names
Molecular Properties
488.4
MW (Da)
4.92
ALogP
6
HBA
3
HBD
97.3
PSA (Ų)
0.34
QED
0
Ro5 Violations
6
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 3 meas. best 7.6
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Non-receptor tyrosine-protein kinase TYK2 CHEMBL3553 | IC50 | 7.6 | 6.83 | 25.0 | 3 |
Pharmacokinetic Data
| Parameter | Value | Units | Species |
|---|---|---|---|
| Fu | 0.004 | - | Homo sapiens |
| Fu | 0.005 | - | Rattus norvegicus |
| Fu | 0.004 | - | Mus musculus |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Non-receptor tyrosine-protein kinase TYK2 | IC50 | = | 25.0 | nM | 7.6 | Displacement of [3H]-(R)-N-(1-(3-(8-methyl-5-(methylamino)-8H-imidazo[4,5-d]thia... | 30108788 |
| Non-receptor tyrosine-protein kinase TYK2 | IC50 | = | 320.0 | nM | 6.5 | Inhibition of TYK2 JH2 domain in IFNalpha-stimulated human Kit225 T cells by luc... | 30108788 |
| Non-receptor tyrosine-protein kinase TYK2 | IC50 | = | 410.0 | nM | 6.39 | Inhibition of TYK2 JH2 domain in IL23-stimulated human Kit225 T cells by lucifer... | 30108788 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 30108788 | 10.1039/C6MD00560H | ADMET | 6 |
| 30108788 | 10.1039/C6MD00560H | Non-receptor tyrosine-protein kinase TYK2 | 4 |
| 30108788 | 10.1039/C6MD00560H | 3',5'-cyclic-AMP phosphodiesterase 4D | 1 |
Data from ChEMBL 36 via Core Engine