Compound Detail
CHEMBL4558996
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Basic Information
| ChEMBL ID | CHEMBL4558996 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | RQMFGOKECSDXFT-UHFFFAOYSA-N |
| Parent Compound | CHEMBL4597732 |
| Active Moiety | CHEMBL4597732 |
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names
Molecular Properties
382.5
MW (Da)
2.58
ALogP
9
HBA
1
HBD
83.0
PSA (Ų)
0.72
QED
0
Ro5 Violations
5
Rot. Bonds
Drug Information
| Molecule Type | Unknown |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 2 meas. best 6.91
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Mast/stem cell growth factor receptor Kit CHEMBL1936 | IC50 | 6.91 | 6.91 | 123.0 | 1 |
| Receptor-type tyrosine-protein kinase FLT3 CHEMBL1974 | IC50 | 6.79 | 6.79 | 163.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Mast/stem cell growth factor receptor Kit | IC50 | = | 123.0 | nM | 6.91 | Inhibition of recombinant N-terminal 6x-His-tagged c-KIT (547 to 935 residues)/(... | 31721578 |
| Receptor-type tyrosine-protein kinase FLT3 | IC50 | = | 163.0 | nM | 6.79 | Inhibition of wild type recombinant GST-tagged FLT3 (Y567 to S993 residues) (unk... | 31721578 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 31721578 | 10.1021/acs.jmedchem.9b01229 | Mast/stem cell growth factor receptor Kit | 1 |
| 31721578 | 10.1021/acs.jmedchem.9b01229 | Receptor-type tyrosine-protein kinase FLT3 | 1 |
| 31721578 | 10.1021/acs.jmedchem.9b01229 | GISTT1 | 1 |
| 31721578 | 10.1021/acs.jmedchem.9b01229 | MOLM-13 | 1 |
Data from ChEMBL 36 via Core Engine