Compound Detail
CHEMBL5563675
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Cc1cc2n(n1)CCN(C(=O)c1c(N)n(-c3c(C)ccc(O)c3C)c3nc(C)c(C)nc13)C2
Basic Information
| ChEMBL ID | CHEMBL5563675 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | VSZLUQMOTCYHTO-UHFFFAOYSA-N |
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names
Molecular Properties
445.5
MW (Da)
3.10
ALogP
8
HBA
2
HBD
115.1
PSA (Ų)
0.49
QED
0
Ro5 Violations
2
Rot. Bonds
Drug Information
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 2 meas. best 8.15
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Myelin transcription factor 1 CHEMBL2331044 | IC50 | 8.15 | 8.15 | 7.1 | 1 |
| Cyclin-dependent kinase 1 CHEMBL308 | IC50 | 6.45 | 6.45 | 358.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Myelin transcription factor 1 | IC50 | = | 7.1 | nM | 8.15 | Inhibition of human recombinant MYT1 incubated for 60 mins in presence of tracer... | 38146659 |
| Cyclin-dependent kinase 1 | IC50 | = | 358.0 | nM | 6.45 | Inhibition of CDK1 phosphorylation at Thr14 residue in human HCC1569 cells incub... | 38146659 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 38146659 | 10.1021/acs.jmedchem.3c01476 | Myelin transcription factor 1 | 1 |
| 38146659 | 10.1021/acs.jmedchem.3c01476 | Wee1-like protein kinase | 1 |
| 38146659 | 10.1021/acs.jmedchem.3c01476 | Cyclin-dependent kinase 1 | 1 |
Data from ChEMBL 36 via Core Engine