Compound Detail
CHEMBL1669595
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NC(=O)c1nn(-c2ccc(F)cc2)c2c1CCc1ccc(NC(=O)c3cc(N4CCN(Cc5cnn(CCCO)c5)CC4)ncc3Cl)cc1-2
Basic Information
| ChEMBL ID | CHEMBL1669595 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | LWGAEQZMVWXORJ-UHFFFAOYSA-N |
2
Targets
2
Activities
1
Assay Types
3
PK Parameters
4
Publications
0
Known Names
Molecular Properties
684.2
MW (Da)
4.08
ALogP
10
HBA
3
HBD
147.4
PSA (Ų)
0.20
QED
1
Ro5 Violations
10
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 2 meas. best 8.66
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Inhibitor of nuclear factor kappa-B kinase subunit beta CHEMBL1991 | IC50 | 8.66 | 8.66 | 2.2 | 1 |
| PBMC CHEMBL613107 | IC50 | 7.82 | 7.82 | 15.0 | 1 |
Pharmacokinetic Data
| Parameter | Value | Units | Species |
|---|---|---|---|
| T1/2 | 5.0 | hr | Homo sapiens |
| T1/2 | 4.0 | hr | Homo sapiens |
| T1/2 | 0.15 | 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 | = | 2.2 | nM | 8.66 | Inhibition of human recombinant IKK2 in human PBMC | 21236687 |
| PBMC | IC50 | = | 15.0 | nM | 7.82 | 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 | 3 |
| 21236687 | 10.1016/j.bmc.2010.12.027 | PBMC | 1 |
| 21236687 | 10.1016/j.bmc.2010.12.027 | Liver microsomes | 1 |
| 21236687 | 10.1016/j.bmc.2010.12.027 | Voltage-gated inwardly rectifying potassium channel KCNH2 | 1 |
Data from ChEMBL 36 via Core Engine