Compound Detail
CHEMBL211011
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CC1(C)C(=O)Nc2ccc(N[C@H](COc3cncc(-c4ccc5c(c4)C(C)(C)C(=O)N5)c3)Cc3c[nH]c4ccccc34)cc21
Basic Information
| ChEMBL ID | CHEMBL211011 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | BFSKCZOPLXJESU-VWLOTQADSA-N |
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names
Molecular Properties
585.7
MW (Da)
6.79
ALogP
5
HBA
4
HBD
108.1
PSA (Ų)
0.16
QED
2
Ro5 Violations
8
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 2 meas. best 7.61
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| RAC-alpha serine/threonine-protein kinase CHEMBL4282 | IC50 | 7.61 | 7.61 | 24.6 | 1 |
| F5.12 CHEMBL614948 | IC50 | 5.57 | 5.57 | 2700.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| RAC-alpha serine/threonine-protein kinase | IC50 | = | 24.6 | nM | 7.61 | Inhibition of AKT1 in presence of 5 uM ATP | 16644221 |
| F5.12 | IC50 | = | 2700.0 | nM | 5.57 | Cytotoxicity against F5.12-Akt cells by MTT assay in presence of 5 uM ATP | 16644221 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 16644221 | 10.1016/j.bmcl.2006.04.005 | F5.12 | 1 |
| 16644221 | 10.1016/j.bmcl.2006.04.005 | RAC-alpha serine/threonine-protein kinase | 1 |
Data from ChEMBL 36 via Core Engine