Compound Detail
CHEMBL1825100
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Basic Information
| ChEMBL ID | CHEMBL1825100 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | SRJYCUWWNQFSQR-UHFFFAOYSA-N |
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names
Molecular Properties
445.6
MW (Da)
2.62
ALogP
9
HBA
2
HBD
126.1
PSA (Ų)
0.53
QED
0
Ro5 Violations
7
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 4 meas. best 8.4
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Cyclin-dependent kinase 1/cyclin B1 CHEMBL1907602 | IC50 | 8.4 | 8.4 | 4.0 | 1 |
| Aurora kinase A CHEMBL4722 | IC50 | 6.96 | 6.96 | 110.0 | 1 |
| HCT-116 CHEMBL394 | IC50 | 6.84 | 6.84 | 145.0 | 1 |
| K562 CHEMBL385 | IC50 | 6.52 | 6.52 | 300.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Cyclin-dependent kinase 1/cyclin B1 | IC50 | = | 4.0 | nM | 8.4 | Inhibition of CDK1/Cyclin B assessed as phosphorylation of Z-lyte Peptide at 0.0... | 21798738 |
| Aurora kinase A | IC50 | = | 110.0 | nM | 6.96 | Inhibition of Aurora kinase A assessed as phosphorylation of Lats2 substrate at ... | 21798738 |
| HCT-116 | IC50 | = | 145.0 | nM | 6.84 | Cytotoxicity against human HCT116 cells assessed as growth inhibition at 0.01 to... | 21798738 |
| K562 | IC50 | = | 300.0 | nM | 6.52 | Cell cycle arrest in human K562 cells assessed as accumulation of cells at G2/M ... | 21798738 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 21798738 | 10.1016/j.bmcl.2011.06.129 | Cyclin-dependent kinase 1/cyclin B1 | 1 |
| 21798738 | 10.1016/j.bmcl.2011.06.129 | Aurora kinase A | 1 |
| 21798738 | 10.1016/j.bmcl.2011.06.129 | HCT-116 | 1 |
| 21798738 | 10.1016/j.bmcl.2011.06.129 | K562 | 1 |
Data from ChEMBL 36 via Core Engine