Compound Detail
CHEMBL5597417
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Basic Information
| ChEMBL ID | CHEMBL5597417 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | PBIGREVGMNJQFD-UHFFFAOYSA-N |
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
7
Publications
0
Known Names
Molecular Properties
482.0
MW (Da)
3.98
ALogP
9
HBA
3
HBD
114.1
PSA (Ų)
0.21
QED
0
Ro5 Violations
12
Rot. Bonds
Drug Information
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 2 meas. best 6.46
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Histone deacetylase 3 CHEMBL1829 | IC50 | 6.46 | 6.46 | 350.9 | 1 |
| Histone deacetylase 1 CHEMBL325 | IC50 | 6.17 | 6.17 | 679.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Histone deacetylase 3 | IC50 | = | 350.9 | nM | 6.46 | Inhibition of human recombinant HDAC3 using Ac-Lys-Tyr-Lys(eta-acetyl)-AMC as su... | 39178382 |
| Histone deacetylase 1 | IC50 | = | 679.0 | nM | 6.17 | Inhibition of human recombinant HDAC1 using Ac-Lys-Tyr-Lys(eta-acetyl)-AMC as su... | 39178382 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 39178382 | 10.1021/acs.jmedchem.4c00837 | Cyclin-dependent kinase 9 | 1 |
| 39178382 | 10.1021/acs.jmedchem.4c00837 | Histone deacetylase 1 | 1 |
| 39178382 | 10.1021/acs.jmedchem.4c00837 | Histone deacetylase 3 | 1 |
| 39178382 | 10.1021/acs.jmedchem.4c00837 | Histone deacetylase 6 | 1 |
| 39178382 | 10.1021/acs.jmedchem.4c00837 | Cyclin-dependent kinase 2 | 1 |
| 39178382 | 10.1021/acs.jmedchem.4c00837 | Cyclin-dependent kinase 7 | 1 |
| 39178382 | 10.1021/acs.jmedchem.4c00837 | Histone deacetylase 4 | 1 |
Data from ChEMBL 36 via Core Engine