Compound Detail
CHEMBL4753530
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Basic Information
| ChEMBL ID | CHEMBL4753530 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | MPNRAWQJWKZFQV-UHFFFAOYSA-N |
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names
Molecular Properties
462.6
MW (Da)
4.01
ALogP
9
HBA
2
HBD
110.5
PSA (Ų)
0.45
QED
0
Ro5 Violations
6
Rot. Bonds
Drug Information
| Molecule Type | Unknown |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 1 meas. best 8.0
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Tyrosine-protein kinase BTK CHEMBL5251 | IC50 | 8.0 | 8.0 | 10.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Tyrosine-protein kinase BTK | IC50 | = | 10.0 | nM | 8.0 | Inhibition of recombinant human full-length N-terminal His6-tagged BTK expressed... | 32696648 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 32696648 | 10.1021/acs.jmedchem.0c00702 | No relevant target | 2 |
| 32696648 | 10.1021/acs.jmedchem.0c00702 | Tyrosine-protein kinase BTK | 1 |
Data from ChEMBL 36 via Core Engine