Compound Detail
CHEMBL4285083
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C=CC(=O)N[C@H]1CCN(c2ccc(C(N)=O)c(Nc3ccc(C(=O)N4CC(C)OC(C)C4)cc3)n2)C1
Basic Information
| ChEMBL ID | CHEMBL4285083 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | GZXNPYNLEUZRFM-UHYCVJNDSA-N |
1
Targets
1
Activities
1
Assay Types
3
PK Parameters
3
Publications
0
Known Names
Molecular Properties
492.6
MW (Da)
2.05
ALogP
7
HBA
3
HBD
129.9
PSA (Ų)
0.50
QED
0
Ro5 Violations
7
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 1 meas. best 8.55
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Tyrosine-protein kinase BTK CHEMBL5251 | IC50 | 8.55 | 8.55 | 2.8 | 1 |
Pharmacokinetic Data
| Parameter | Value | Units | Species |
|---|---|---|---|
| CL | 18.0 | uL/min | Homo sapiens |
| CL | 30.0 | uL/min | Mus musculus |
| CL | 10.0 | uL/min | Rattus norvegicus |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Tyrosine-protein kinase BTK | IC50 | = | 2.8 | nM | 8.55 | Inhibition of full length human BTK (8 to 80 residues) using FITC-AHA-EEPLYWSFPA... | 30243592 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 30243592 | 10.1016/j.bmcl.2018.09.018 | ADMET | 5 |
| 30243592 | 10.1016/j.bmcl.2018.09.018 | Tyrosine-protein kinase BTK | 1 |
| 30243592 | 10.1016/j.bmcl.2018.09.018 | Voltage-gated inwardly rectifying potassium channel KCNH2 | 1 |
Data from ChEMBL 36 via Core Engine