Compound Detail
CHEMBL598406
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Basic Information
| ChEMBL ID | CHEMBL598406 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | KHRPCRNETLJSDS-INIZCTEOSA-N |
3
Targets
3
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names
Molecular Properties
456.5
MW (Da)
4.79
ALogP
7
HBA
3
HBD
105.6
PSA (Ų)
0.20
QED
0
Ro5 Violations
12
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 3 meas. best 6.9
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Epidermal growth factor receptor CHEMBL203 | IC50 | 6.9 | 6.9 | 125.6 | 1 |
| Histone deacetylase CHEMBL2093865 | IC50 | 6.78 | 6.78 | 165.3 | 1 |
| Receptor tyrosine-protein kinase erbB-2 CHEMBL1824 | IC50 | 6.76 | 6.76 | 175.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Epidermal growth factor receptor | IC50 | = | 125.6 | nM | 6.9 | Inhibition of EGFR | 20143778 |
| Histone deacetylase | IC50 | = | 165.3 | nM | 6.78 | Inhibition of HDAC in human HeLa cell nuclear extract | 20143778 |
| Receptor tyrosine-protein kinase erbB-2 | IC50 | = | 175.0 | nM | 6.76 | Inhibition of HER2 | 20143778 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 20143778 | 10.1021/jm901453q | Histone deacetylase | 1 |
| 20143778 | 10.1021/jm901453q | Epidermal growth factor receptor | 1 |
| 20143778 | 10.1021/jm901453q | Receptor tyrosine-protein kinase erbB-2 | 1 |
Data from ChEMBL 36 via Core Engine