Compound Detail
CHEMBL249303
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Basic Information
| ChEMBL ID | CHEMBL249303 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | HAIHTRCFSLFERU-UHFFFAOYSA-N |
8
Targets
9
Activities
1
Assay Types
0
PK Parameters
9
Publications
0
Known Names
Molecular Properties
447.6
MW (Da)
5.56
ALogP
5
HBA
2
HBD
86.4
PSA (Ų)
0.35
QED
1
Ro5 Violations
6
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 9 meas. best 8.74
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Cyclin-dependent kinase 1 CHEMBL308 | IC50 | 8.74 | 8.74 | 1.8 | 1 |
| HeLa CHEMBL399 | IC50 | 7.54 | 7.54 | 29.0 | 1 |
| HCT-116 CHEMBL394 | IC50 | 7.51 | 7.51 | 31.0 | 1 |
| A-375 CHEMBL613859 | IC50 | 7.33 | 7.33 | 47.0 | 1 |
| Receptor tyrosine-protein kinase erbB-2 CHEMBL1824 | IC50 | 7.05 | 7.05 | 89.0 | 1 |
| Proto-oncogene tyrosine-protein kinase receptor Ret CHEMBL2041 | IC50 | 6.0 | 6.0 | 1000.0 | 2 |
| Unchecked CHEMBL612545 | IC50 | 6.0 | 6.0 | 1000.0 | 1 |
| Vascular endothelial growth factor receptor 2 CHEMBL279 | IC50 | 5.81 | 5.81 | 1550.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Cyclin-dependent kinase 1 | IC50 | = | 1.8 | nM | 8.74 | Inhibition of CDK1 | 17532631 |
| HeLa | IC50 | = | 29.0 | nM | 7.54 | Antiproliferative activity against human HeLa cells | 17532631 |
| HCT-116 | IC50 | = | 31.0 | nM | 7.51 | Antiproliferative activity against human HCT116 cells | 17532631 |
| A-375 | IC50 | = | 47.0 | nM | 7.33 | Antiproliferative activity against human A375 cells | 17532631 |
| Receptor tyrosine-protein kinase erbB-2 | IC50 | = | 89.0 | nM | 7.05 | Inhibition of HER2 | 17532631 |
| Unchecked | IC50 | = | 1000.0 | nM | 6.0 | Inhibition of Aurora2 | 17532631 |
| Proto-oncogene tyrosine-protein kinase receptor Ret | IC50 | = | 1000.0 | nM | 6.0 | Inhibition of RET | 17532631 |
| Proto-oncogene tyrosine-protein kinase receptor Ret | IC50 | = | 1000.0 | nM | 6.0 | Inhibition of RET kinase | 21724393 |
| Vascular endothelial growth factor receptor 2 | IC50 | = | 1550.0 | nM | 5.81 | Inhibition of VEGFR2 | 17532631 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 17532631 | 10.1016/j.bmcl.2007.05.029 | Cyclin-dependent kinase 1 | 1 |
| 17532631 | 10.1016/j.bmcl.2007.05.029 | Vascular endothelial growth factor receptor 2 | 1 |
| 17532631 | 10.1016/j.bmcl.2007.05.029 | Unchecked | 1 |
| 17532631 | 10.1016/j.bmcl.2007.05.029 | HeLa | 1 |
| 17532631 | 10.1016/j.bmcl.2007.05.029 | HCT-116 | 1 |
| 17532631 | 10.1016/j.bmcl.2007.05.029 | A-375 | 1 |
| 17532631 | 10.1016/j.bmcl.2007.05.029 | Receptor tyrosine-protein kinase erbB-2 | 1 |
| 17532631 | 10.1016/j.bmcl.2007.05.029 | Proto-oncogene tyrosine-protein kinase receptor Ret | 1 |
| 21724393 | 10.1016/j.bmcl.2011.06.003 | Proto-oncogene tyrosine-protein kinase receptor Ret | 1 |
Data from ChEMBL 36 via Core Engine