Compound Detail
CHEMBL470597
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Basic Information
| ChEMBL ID | CHEMBL470597 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | FLJNUPIJNHQZPV-AWEZNQCLSA-N |
7
Targets
9
Activities
2
Assay Types
0
PK Parameters
7
Publications
0
Known Names
Molecular Properties
455.4
MW (Da)
4.35
ALogP
4
HBA
3
HBD
83.8
PSA (Ų)
0.40
QED
0
Ro5 Violations
6
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 7 meas. best 9.0
Ki 2 meas. best 10.22
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| RAC-alpha serine/threonine-protein kinase CHEMBL4282 | Ki | 10.22 | 10.22 | 0.1 | 1 |
| RAC-alpha serine/threonine-protein kinase CHEMBL4282 | IC50 | 9.0 | 9.0 | 1.0 | 1 |
| RAC-gamma serine/threonine-protein kinase CHEMBL4816 | IC50 | 8.7 | 8.7 | 2.0 | 1 |
| RAC-beta serine/threonine-protein kinase CHEMBL2431 | Ki | 8.52 | 8.52 | 3.0 | 1 |
| RAC-beta serine/threonine-protein kinase CHEMBL2431 | IC50 | 8.0 | 8.0 | 10.0 | 1 |
| LNCaP CHEMBL612518 | IC50 | 7.68 | 7.68 | 21.0 | 1 |
| HFF CHEMBL614071 | IC50 | 7.05 | 7.05 | 90.0 | 1 |
| Unchecked CHEMBL612545 | IC50 | 7.0 | 7.0 | 100.0 | 1 |
| BT-474 CHEMBL614529 | IC50 | 6.64 | 6.64 | 230.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| RAC-alpha serine/threonine-protein kinase | Ki | = | 0.06 | nM | 10.22 | Inhibition of AKT1 | 19285393 |
| RAC-alpha serine/threonine-protein kinase | IC50 | = | 1.0 | nM | 9.0 | Inhibition of AKT1 | 19285393 |
| RAC-gamma serine/threonine-protein kinase | IC50 | = | 2.0 | nM | 8.7 | Inhibition of AKT3 | 19285393 |
| RAC-beta serine/threonine-protein kinase | Ki | = | 3.0 | nM | 8.52 | Inhibition of AKT2 | 19285393 |
| RAC-beta serine/threonine-protein kinase | IC50 | = | 10.0 | nM | 8.0 | Inhibition of AKT2 | 19285393 |
| LNCaP | IC50 | = | 21.0 | nM | 7.68 | Cytotoxicity against human LNCAP cells | 19285393 |
| HFF | IC50 | = | 90.0 | nM | 7.05 | Cytotoxicity against human HFF cells | 19285393 |
| Unchecked | IC50 | = | 100.0 | nM | 7.0 | Inhibition of AKT-mediated GSK3-beta phosphorylation in human BT474 cells by mec... | 19285393 |
| BT-474 | IC50 | = | 230.0 | nM | 6.64 | Cytotoxicity against human BT474 cells | 19285393 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 19285393 | 10.1016/j.bmcl.2009.02.094 | RAC-alpha serine/threonine-protein kinase | 2 |
| 19285393 | 10.1016/j.bmcl.2009.02.094 | RAC-beta serine/threonine-protein kinase | 2 |
| 19285393 | 10.1016/j.bmcl.2009.02.094 | Unchecked | 1 |
| 19285393 | 10.1016/j.bmcl.2009.02.094 | RAC-gamma serine/threonine-protein kinase | 1 |
| 19285393 | 10.1016/j.bmcl.2009.02.094 | BT-474 | 1 |
| 19285393 | 10.1016/j.bmcl.2009.02.094 | LNCaP | 1 |
| 19285393 | 10.1016/j.bmcl.2009.02.094 | HFF | 1 |
Data from ChEMBL 36 via Core Engine