Compound Detail
CHEMBL7553
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Basic Information
| ChEMBL ID | CHEMBL7553 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | JRIVCRNBEGQLHN-UHFFFAOYSA-N |
2
Targets
3
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names
Molecular Properties
353.4
MW (Da)
2.89
ALogP
7
HBA
0
HBD
73.1
PSA (Ų)
0.53
QED
0
Ro5 Violations
4
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 3 meas. best 5.8
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| GABA-A receptor; anion channel CHEMBL1907607 | IC50 | 5.8 | 5.8 | 1584.9 | 2 |
| Unchecked CHEMBL612545 | IC50 | 5.8 | 5.8 | 1584.9 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| GABA-A receptor; anion channel | IC50 | = | 1600.0 | nM | 5.8 | Concentration that inhibits binding of 1.5 nM [3H]diazepam to rat brain benzodia... | 2540330 |
| Unchecked | IC50 | = | 1584.89 | nM | 5.8 | Displacement of [3H]diazepam from benzodiazepine receptor in rat brain | 18346822 |
| GABA-A receptor; anion channel | IC50 | = | 1584.89 | nM | 5.8 | Binding affinity to Rattus norvegicus (rat) brain GABA-A receptor benzodiazepine... | - |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 2540330 | 10.1021/jm00125a015 | GABA-A receptor; anion channel | 1 |
| 2540330 | 10.1021/jm00125a015 | 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