Assay Detail
Binding
CHEMBL3618901
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Binding affinity to human 5HT1F receptor by radioligand binding assay
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Binding |
| Organism | Homo sapiens |
| Confidence | 9 — Direct single protein target |
| Curated By | Autocuration |
Publication
Discovery of selective N-[3-(1-methyl-piperidine-4-carbonyl)-phenyl]-benzamide-based 5-HT₁ F receptor agonists: Evolution from bicyclic to monocyclic cores.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| Ki | 14 | 6.75 | 8.68 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL101690 | — | — | 1 | 8.68 |
| CHEMBL3617549 | — | — | 1 | 8.29 |
| CHEMBL3617550 | — | — | 1 | 8.08 |
| CHEMBL3617557 | — | — | 1 | 8.02 |
| CHEMBL3617552 | — | — | 1 | 7.39 |
| CHEMBL3617553 | — | — | 1 | 6.28 |
| CHEMBL3616488 | — | — | 1 | 6.21 |
| CHEMBL3617555 | — | — | 1 | 6.06 |
| CHEMBL3617556 | — | — | 1 | 5.96 |
| CHEMBL3617551 | — | — | 1 | 5.89 |
| CHEMBL3617554 | — | — | 1 | 5.77 |
| CHEMBL3617560 | — | — | 1 | 5.62 |
| CHEMBL3617559 | — | — | 1 | 5.50 |
| CHEMBL3617558 | — | — | 1 | - |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL101690 | — | Ki | = | 2.1 | nM | 8.68 |
| CHEMBL3617549 | — | Ki | = | 5.1 | nM | 8.29 |
| CHEMBL3617550 | — | Ki | = | 8.3 | nM | 8.08 |
| CHEMBL3617557 | — | Ki | = | 9.5 | nM | 8.02 |
| CHEMBL3617552 | — | Ki | = | 41.0 | nM | 7.39 |
| CHEMBL3617553 | — | Ki | = | 530.0 | nM | 6.28 |
| CHEMBL3616488 | — | Ki | = | 610.0 | nM | 6.21 |
| CHEMBL3617555 | — | Ki | = | 870.0 | nM | 6.06 |
| CHEMBL3617556 | — | Ki | = | 1100.0 | nM | 5.96 |
| CHEMBL3617551 | — | Ki | = | 1300.0 | nM | 5.89 |
| CHEMBL3617554 | — | Ki | = | 1700.0 | nM | 5.77 |
| CHEMBL3617560 | — | Ki | = | 2400.0 | nM | 5.62 |
| CHEMBL3617559 | — | Ki | = | 3200.0 | nM | 5.50 |
| CHEMBL3617558 | — | Ki | - | — | - |