Compound Detail
CHEMBL4877368
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C=CC(=O)N1CCC[C@@H](NC(=O)c2sc3nccc4c3c2NC(=O)N4c2cc(OC(C)C)ccc2C)C1
Basic Information
| ChEMBL ID | CHEMBL4877368 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | RZQRFSYZDSHHJL-QGZVFWFLSA-N |
1
Targets
3
Activities
2
Assay Types
0
PK Parameters
2
Publications
0
Known Names
Molecular Properties
519.6
MW (Da)
4.98
ALogP
6
HBA
2
HBD
103.9
PSA (Ų)
0.45
QED
1
Ro5 Violations
6
Rot. Bonds
Drug Information
| Molecule Type | Unknown |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 2 meas. best 5.6
Ki 1 meas. best 5.48
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Tyrosine-protein kinase BTK CHEMBL5251 | IC50 | 5.6 | 5.6 | 2512.0 | 2 |
| Tyrosine-protein kinase BTK CHEMBL5251 | Ki | 5.48 | 5.48 | 3290.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Tyrosine-protein kinase BTK | IC50 | = | 2512.0 | nM | 5.6 | TBD: TBD | - |
| Tyrosine-protein kinase BTK | IC50 | = | 2512.0 | nM | 5.6 | Kinase Lanthascreen Binding Assay: A BTK kinase lanthascreen binding assay monit... | - |
| Tyrosine-protein kinase BTK | Ki | = | 3290.0 | nM | 5.48 | Covalent inhibition of recombinant human GST-tagged BTK (2 to 659 end residues) ... | 34055226 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 34055226 | 10.1021/acsmedchemlett.1c00044 | Tyrosine-protein kinase BTK | 4 |
| 34055226 | 10.1021/acsmedchemlett.1c00044 | Unchecked | 1 |
Data from ChEMBL 36 via Core Engine