Compound Detail
CHEMBL388429
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Basic Information
| ChEMBL ID | CHEMBL388429 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | QDGMLNPUKKIWDJ-WYMLVPIESA-N |
3
Targets
4
Activities
2
Assay Types
0
PK Parameters
3
Publications
0
Known Names
Molecular Properties
446.5
MW (Da)
3.63
ALogP
6
HBA
2
HBD
105.5
PSA (Ų)
0.20
QED
0
Ro5 Violations
6
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 3 meas. best 7.05
EC50 1 meas. best 5.57
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Histone deacetylase CHEMBL2093865 | IC50 | 7.05 | 7.05 | 90.0 | 1 |
| Histone deacetylase 1 CHEMBL325 | IC50 | 6.7 | 6.7 | 200.0 | 1 |
| Histone deacetylase CHEMBL2093865 | EC50 | 5.57 | 5.57 | 2670.0 | 1 |
| HeLa CHEMBL399 | IC50 | 5.54 | 5.54 | 2880.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Histone deacetylase | IC50 | = | 90.0 | nM | 7.05 | Inhibition of HDAC in HeLa cells | 17691763 |
| Histone deacetylase 1 | IC50 | = | 200.0 | nM | 6.7 | Inhibition of recombinant HDAC1 in HeLa cells | 17691763 |
| Histone deacetylase | EC50 | = | 2670.0 | nM | 5.57 | Inhibition of HDAC in HeLa cells assessed as induction of human histone H3 hyper... | 17691763 |
| HeLa | IC50 | = | 2880.0 | nM | 5.54 | Cytotoxicity against HeLa cells | 17691763 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 17691763 | 10.1021/jm0703136 | Histone deacetylase | 2 |
| 17691763 | 10.1021/jm0703136 | Histone deacetylase 1 | 1 |
| 17691763 | 10.1021/jm0703136 | HeLa | 1 |
Data from ChEMBL 36 via Core Engine