Compound Detail
CHEMBL292555
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Basic Information
| ChEMBL ID | CHEMBL292555 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | SIOLCBSXVMEFJP-UHFFFAOYSA-N |
2
Targets
3
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names
Molecular Properties
339.4
MW (Da)
1.57
ALogP
7
HBA
1
HBD
79.2
PSA (Ų)
0.69
QED
0
Ro5 Violations
6
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 3 meas. best 6.96
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| GABA-A receptor; anion channel CHEMBL1907607 | IC50 | 6.96 | 6.96 | 109.7 | 2 |
| Unchecked CHEMBL612545 | IC50 | 6.96 | 6.96 | 109.7 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| GABA-A receptor; anion channel | IC50 | = | 110.0 | nM | 6.96 | Inhibition of specific binding of 1.5 nM [3H]diazepam to rat brain benzodiazepin... | 1967311 |
| Unchecked | IC50 | = | 109.65 | nM | 6.96 | Displacement of [3H]diazepam from benzodiazepine receptor in rat brain | 18346822 |
| GABA-A receptor; anion channel | IC50 | = | 109.65 | nM | 6.96 | Binding affinity to Rattus norvegicus (rat) brain GABA-A receptor benzodiazepine... | - |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 1967311 | 10.1021/jm00163a032 | GABA-A receptor; anion channel | 1 |
| 1967311 | 10.1021/jm00163a032 | Rattus norvegicus | 1 |
| 18346822 | 10.1016/j.ejmech.2008.01.030 | Unchecked | 1 |
| - | 10.1007/s00044-008-9111-6 | GABA-A receptor; anion channel | 1 |
Data from ChEMBL 36 via Core Engine