Compound Detail
CHEMBL5565411
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Basic Information
| ChEMBL ID | CHEMBL5565411 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | CIYSXNZXVUDYKU-UHFFFAOYSA-N |
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names
Molecular Properties
335.4
MW (Da)
3.19
ALogP
5
HBA
1
HBD
72.0
PSA (Ų)
0.80
QED
0
Ro5 Violations
3
Rot. Bonds
Drug Information
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 2 meas. best 8.7
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform CHEMBL4005 | IC50 | 8.7 | 8.7 | 2.0 | 1 |
| RAC-alpha serine/threonine-protein kinase CHEMBL4282 | IC50 | 7.4 | 7.4 | 40.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform | IC50 | = | 2.0 | nM | 8.7 | Inhibition of PI3Kalpha (unknown origin) by kinase profiling assay | 37683364 |
| RAC-alpha serine/threonine-protein kinase | IC50 | = | 40.0 | nM | 7.4 | Inhibition of AKT phosphorylation in human OVCAR-8 cells assessed as reduction i... | 37683364 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 37683364 | 10.1016/j.ejmech.2023.115762 | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform | 1 |
| 37683364 | 10.1016/j.ejmech.2023.115762 | RAC-alpha serine/threonine-protein kinase | 1 |
Data from ChEMBL 36 via Core Engine