Compound Detail
CHEMBL597569
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Basic Information
| ChEMBL ID | CHEMBL597569 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | FEOPLVISXFSHGK-UHFFFAOYSA-N |
3
Targets
4
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names
Molecular Properties
507.0
MW (Da)
5.03
ALogP
8
HBA
3
HBD
114.8
PSA (Ų)
0.16
QED
2
Ro5 Violations
14
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 4 meas. best 8.08
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Histone deacetylase CHEMBL2093865 | IC50 | 8.08 | 8.08 | 8.4 | 1 |
| Epidermal growth factor receptor CHEMBL203 | IC50 | 7.98 | 7.98 | 10.4 | 1 |
| Receptor tyrosine-protein kinase erbB-2 CHEMBL1824 | IC50 | 7.62 | 7.31 | 24.0 | 2 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Histone deacetylase | IC50 | = | 8.4 | nM | 8.08 | Inhibition of HDAC in human HeLa cell nuclear extract | 20143778 |
| Epidermal growth factor receptor | IC50 | = | 10.4 | nM | 7.98 | Inhibition of EGFR | 20143778 |
| Receptor tyrosine-protein kinase erbB-2 | IC50 | = | 24.0 | nM | 7.62 | Inhibition of HER2 | 20143778 |
| Receptor tyrosine-protein kinase erbB-2 | IC50 | = | 100.0 | nM | 7.0 | Inhibition of N-terminal GST-tagged human HER2 (Lys676 to Val1255 residues) expr... | - |
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