Compound Detail
CHEMBL81626
Enter ChEMBL ID:
Free Research Context
This compound will appear in recent viewed items on the research home for this browser.
Research home
View demo workspace
Basic Information
| ChEMBL ID | CHEMBL81626 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | WIULPOAMZNPPJM-UHFFFAOYSA-N |
4
Targets
6
Activities
1
Assay Types
0
PK Parameters
8
Publications
0
Known Names
Molecular Properties
295.4
MW (Da)
5.39
ALogP
1
HBA
3
HBD
47.9
PSA (Ų)
0.52
QED
1
Ro5 Violations
4
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 6 meas. best 6.62
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Sigma non-opioid intracellular receptor 1 CHEMBL287 | IC50 | 6.62 | 6.595 | 242.0 | 2 |
| Sodium channel protein type 2 subunit alpha CHEMBL3399 | IC50 | 6.34 | 6.34 | 460.0 | 1 |
| Glutamate NMDA receptor CHEMBL1907608 | IC50 | 4.75 | 4.69 | 17900.0 | 2 |
| Glutamate [NMDA] receptor CHEMBL2094124 | IC50 | 4.57 | 4.57 | 26800.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Sigma non-opioid intracellular receptor 1 | IC50 | = | 242.0 | nM | 6.62 | Tested in vitro for the concentration required to inhibit specific [3H]DTG radio... | 8295213 |
| Sigma non-opioid intracellular receptor 1 | IC50 | = | 270.0 | nM | 6.57 | In vitro inhibitory activity against [3H]DTG binding to Sigma opioid receptor in... | 1975275 |
| Sodium channel protein type 2 subunit alpha | IC50 | = | 460.0 | nM | 6.34 | Sodium channel block, determined by % block of [14C]guanidinium flux in CHO line... | 9703475 |
| Glutamate NMDA receptor | IC50 | = | 17900.0 | nM | 4.75 | Displacement of [3H]MK-801 from rat brain membrane N-methyl-D-aspartate glutamat... | 9703475 |
| Glutamate NMDA receptor | IC50 | = | 23200.0 | nM | 4.63 | In vitro concentration required to inhibit specific [3H]MK-801 radioligand bindi... | 8295213 |
| Glutamate [NMDA] receptor | IC50 | = | 26800.0 | nM | 4.57 | In vitro inhibitory activity against [3H](+)-MK-801 binding to PCP receptor in g... | 1975275 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 9703475 | 10.1021/jm980134b | Sodium channel protein type 2 subunit alpha | 1 |
| 9703475 | 10.1021/jm980134b | Glutamate NMDA receptor | 1 |
| 9703475 | 10.1021/jm980134b | Unchecked | 1 |
| 9703475 | 10.1021/jm980134b | No relevant target | 1 |
| 8295213 | 10.1021/jm00028a009 | Glutamate NMDA receptor | 1 |
| 8295213 | 10.1021/jm00028a009 | Sigma non-opioid intracellular receptor 1 | 1 |
| 1975275 | 10.1021/jm00171a016 | Sigma non-opioid intracellular receptor 1 | 1 |
| 1975275 | 10.1021/jm00171a016 | Glutamate [NMDA] receptor | 1 |
Data from ChEMBL 36 via Core Engine