Compound Detail
CHEMBL5798442
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Basic Information
| ChEMBL ID | CHEMBL5798442 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | NJXVAAHYUFZELV-UHFFFAOYSA-N |
5
Targets
5
Activities
1
Assay Types
0
PK Parameters
0
Publications
0
Known Names
Molecular Properties
481.6
MW (Da)
3.97
ALogP
8
HBA
2
HBD
78.4
PSA (Ų)
0.57
QED
0
Ro5 Violations
5
Rot. Bonds
Drug Information
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 5 meas. best 8.46
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Cyclin-dependent kinase 4 CHEMBL331 | IC50 | 8.46 | 8.46 | 3.5 | 1 |
| Cyclin-dependent kinase 6 CHEMBL2508 | IC50 | 8.35 | 8.35 | 4.5 | 1 |
| CDK2/Cyclin A2 CHEMBL3038469 | IC50 | 7.6 | 7.6 | 25.0 | 1 |
| Cyclin-dependent kinase 1/G2/mitotic-specific cyclin-B CHEMBL6066545 | IC50 | 6.8 | 6.8 | 158.0 | 1 |
| Macrophage colony-stimulating factor 1 receptor CHEMBL1844 | IC50 | 6.12 | 6.12 | 752.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Cyclin-dependent kinase 4 | IC50 | = | 3.5 | nM | 8.46 | In Vitro Kinase Inhibition Assay: CDK4 and CDK6: IC50 values of compounds agains... | - |
| Cyclin-dependent kinase 6 | IC50 | = | 4.5 | nM | 8.35 | In Vitro Kinase Inhibition Assay: CDK4 and CDK6: IC50 values of compounds agains... | - |
| CDK2/Cyclin A2 | IC50 | = | 25.0 | nM | 7.6 | Z′-LYTE Assay: CDK5 (p25): IC50 values of compounds against CDK5 (p25) were dete... | - |
| Cyclin-dependent kinase 1/G2/mitotic-specific cyclin-B | IC50 | = | 158.0 | nM | 6.8 | In Vitro Kinase Inhibition Assay: CDK1 (cyclin B): IC50 values of compounds agai... | - |
| Macrophage colony-stimulating factor 1 receptor | IC50 | = | 752.0 | nM | 6.12 | LanthaScreen Eu Kinase Binding Assay: FMS: IC50 values of compounds against FMS ... | - |
Data from ChEMBL 36 via Core Engine