Compound Detail
CHEMBL4460150
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C=CC(=O)Nc1ccccc1Nc1nc(Nc2ccc(N3CCN(C)CC3)cc2)ncc1OCc1ccc(C)cc1
Basic Information
| ChEMBL ID | CHEMBL4460150 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | JBYDLAQOMCSHGT-UHFFFAOYSA-N |
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names
Molecular Properties
549.7
MW (Da)
5.73
ALogP
8
HBA
3
HBD
94.7
PSA (Ų)
0.22
QED
2
Ro5 Violations
10
Rot. Bonds
Drug Information
| Molecule Type | Unknown |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 2 meas. best 8.3
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Proto-oncogene tyrosine-protein kinase Src CHEMBL267 | IC50 | 8.3 | 8.3 | 5.0 | 1 |
| Fibroblast growth factor receptor 1 CHEMBL3650 | IC50 | 6.92 | 6.92 | 119.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Proto-oncogene tyrosine-protein kinase Src | IC50 | = | 5.0 | nM | 8.3 | Inhibition of recombinant human His-tagged full length SRC expressed in baculovi... | 31935084 |
| Fibroblast growth factor receptor 1 | IC50 | = | 119.0 | nM | 6.92 | Inhibition of recombinant human His-tagged FGFR1 (308 to 731 residues) expressed... | 31935084 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 31935084 | 10.1021/acs.jmedchem.9b01502 | Mitogen-activated protein kinase kinase kinase 7 | 1 |
| 31935084 | 10.1021/acs.jmedchem.9b01502 | Proto-oncogene tyrosine-protein kinase Src | 1 |
| 31935084 | 10.1021/acs.jmedchem.9b01502 | Fibroblast growth factor receptor 1 | 1 |
Data from ChEMBL 36 via Core Engine