Compound Detail
CHEMBL4793499
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Basic Information
| ChEMBL ID | CHEMBL4793499 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | SRTKLJHYHAVNCM-UHFFFAOYSA-N |
7
Targets
7
Activities
1
Assay Types
0
PK Parameters
8
Publications
0
Known Names
Molecular Properties
470.0
MW (Da)
3.88
ALogP
6
HBA
1
HBD
61.4
PSA (Ų)
0.59
QED
0
Ro5 Violations
6
Rot. Bonds
Drug Information
| Molecule Type | Unknown |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 7 meas. best 7.0
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| RAC-gamma serine/threonine-protein kinase CHEMBL4816 | IC50 | 7.0 | 7.0 | 101.0 | 1 |
| Unchecked CHEMBL612545 | IC50 | 6.9 | 6.9 | 125.0 | 1 |
| Huh-7 CHEMBL614039 | IC50 | 6.55 | 6.55 | 283.0 | 1 |
| Hep 3B2 CHEMBL4296437 | IC50 | 6.27 | 6.27 | 541.0 | 1 |
| HepG2 CHEMBL395 | IC50 | 6.24 | 6.24 | 580.0 | 1 |
| SMMC-7721 CHEMBL613831 | IC50 | 5.9 | 5.9 | 1249.0 | 1 |
| RAC-beta serine/threonine-protein kinase CHEMBL2431 | IC50 | 5.52 | 5.52 | 3050.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| RAC-gamma serine/threonine-protein kinase | IC50 | = | 101.0 | nM | 7.0 | Inhibition of full length human Akt3 S472D mutant using GRPRTSSFAEGKK as substra... | 32007668 |
| Unchecked | IC50 | = | 125.0 | nM | 6.9 | Inhibition of full length human Akt1 S478G mutant using GRPRTSSFAEGKK as substra... | 32007668 |
| Huh-7 | IC50 | = | 283.0 | nM | 6.55 | Cytotoxicity against human Huh-7 cells assessed as reduction in cell viability b... | 32007668 |
| Hep 3B2 | IC50 | = | 541.0 | nM | 6.27 | Cytotoxicity against human Hep3B cells assessed as reduction in cell viability b... | 32007668 |
| HepG2 | IC50 | = | 580.0 | nM | 6.24 | Cytotoxicity against human HepG2 cells assessed as reduction in cell viability b... | 32007668 |
| SMMC-7721 | IC50 | = | 1249.0 | nM | 5.9 | Cytotoxicity against human SMMC-7721 cells assessed as reduction in cell viabili... | 32007668 |
| RAC-beta serine/threonine-protein kinase | IC50 | = | 3050.0 | nM | 5.52 | Inhibition of full length human Akt2 S474D mutant using GRPRTSSFAEGKK as substra... | 32007668 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 32007668 | 10.1016/j.ejmech.2020.112076 | Unchecked | 2 |
| 32007668 | 10.1016/j.ejmech.2020.112076 | RAC-beta serine/threonine-protein kinase | 2 |
| 32007668 | 10.1016/j.ejmech.2020.112076 | RAC-gamma serine/threonine-protein kinase | 2 |
| 32007668 | 10.1016/j.ejmech.2020.112076 | cAMP-dependent protein kinase catalytic subunit alpha | 1 |
| 32007668 | 10.1016/j.ejmech.2020.112076 | HepG2 | 1 |
| 32007668 | 10.1016/j.ejmech.2020.112076 | Hep 3B2 | 1 |
| 32007668 | 10.1016/j.ejmech.2020.112076 | Huh-7 | 1 |
| 32007668 | 10.1016/j.ejmech.2020.112076 | SMMC-7721 | 1 |
Data from ChEMBL 36 via Core Engine