Compound Detail
CHEMBL1669551
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CN1CCN(c2cc(C(=O)Nc3ccc4c(c3)-c3c(c(C(N)=O)nn3-c3cccc(O)c3)CC4)c(Cl)cn2)CC1
Basic Information
| ChEMBL ID | CHEMBL1669551 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | CUSFVIQRVHXXSC-UHFFFAOYSA-N |
2
Targets
2
Activities
1
Assay Types
1
PK Parameters
2
Publications
0
Known Names
Molecular Properties
558.0
MW (Da)
3.49
ALogP
8
HBA
3
HBD
129.6
PSA (Ų)
0.34
QED
1
Ro5 Violations
5
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 2 meas. best 8.92
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Inhibitor of nuclear factor kappa-B kinase subunit beta CHEMBL1991 | IC50 | 8.92 | 8.92 | 1.2 | 1 |
| PBMC CHEMBL613107 | IC50 | 7.05 | 7.05 | 89.0 | 1 |
Pharmacokinetic Data
| Parameter | Value | Units | Species |
|---|---|---|---|
| T1/2 | 1.0 | hr | Homo sapiens |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Inhibitor of nuclear factor kappa-B kinase subunit beta | IC50 | = | 1.2 | nM | 8.92 | Inhibition of human recombinant IKK2 in human PBMC | 21236687 |
| PBMC | IC50 | = | 89.0 | nM | 7.05 | Inhibition of LPS-stimulated TNFalpha release in human PBMC | 21236687 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 21236687 | 10.1016/j.bmc.2010.12.027 | Inhibitor of nuclear factor kappa-B kinase subunit beta | 2 |
| 21236687 | 10.1016/j.bmc.2010.12.027 | PBMC | 1 |
Data from ChEMBL 36 via Core Engine