Compound Detail
CHEMBL3716549
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Basic Information
| ChEMBL ID | CHEMBL3716549 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | RSRKFXROJZFOAM-UHFFFAOYSA-N |
3
Targets
4
Activities
1
Assay Types
0
PK Parameters
0
Publications
0
Known Names
Molecular Properties
437.4
MW (Da)
5.16
ALogP
5
HBA
3
HBD
82.7
PSA (Ų)
0.39
QED
1
Ro5 Violations
4
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 4 meas. best 6.79
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| CDK3/Cyclin E CHEMBL3038471 | IC50 | 6.79 | 6.79 | 163.0 | 1 |
| Cyclin-dependent kinase 2/cyclin E1 CHEMBL1907605 | IC50 | 6.52 | 6.52 | 302.0 | 1 |
| NON-PROTEIN TARGET CHEMBL3879801 | IC50 | 5.57 | 5.49 | 2700.0 | 2 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| CDK3/Cyclin E | IC50 | = | 163.0 | nM | 6.79 | Inhibition of C-terminal His6-tagged human full length Cdk3/N-terminal GST-tagge... | - |
| Cyclin-dependent kinase 2/cyclin E1 | IC50 | = | 302.0 | nM | 6.52 | Inhibition of C-terminal His6-tagged human full length Cdk2/N-terminal GST-tagge... | - |
| NON-PROTEIN TARGET | IC50 | = | 2700.0 | nM | 5.57 | Antiproliferative activity against human SW620 cells assessed as inhibition of c... | - |
| NON-PROTEIN TARGET | IC50 | = | 3900.0 | nM | 5.41 | Antiproliferative activity against human DU145 cells assessed as inhibition of c... | - |
Data from ChEMBL 36 via Core Engine