Assay Detail
Binding
CHEMBL828838
Review assay metadata, readout intent, target linkage, and publication context from the same page.
Inhibition of [3H]spiperone binding to human dopamine receptor D3 expressed in CHO-K1 cells
4
Total Activities
4
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Binding |
| Organism | Homo sapiens |
| Cell Type | CHO-K1 |
| Confidence | 9 — Direct single protein target |
| Curated By | Expert |
Publication
Discovery of 5-arylsulfonamido-3-(pyrrolidin-2-ylmethyl)-1H-indole derivatives as potent, selective 5-HT6 receptor agonists and antagonists.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| Ki | 4 | 6.03 | 6.03 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL606556 | — | — | 1 | 6.03 |
| CHEMBL606547 | — | — | 1 | - |
| CHEMBL609742 | — | — | 1 | - |
| CHEMBL2113386 | — | — | 1 | - |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL606556 | — | Ki | = | 930.0 | nM | 6.03 |
| CHEMBL606547 | — | Ki | > | 1000.0 | nM | - |
| CHEMBL609742 | — | Ki | > | 5000.0 | nM | - |
| CHEMBL2113386 | — | Ki | > | 5000.0 | nM | - |