Assay Detail
Binding
CHEMBL615342
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Inhibition of 20-HETE synthesis in human renal microsomes
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Binding |
| Organism | Homo sapiens |
| Subcellular | Microsome |
| Confidence | 0 — Uncurated / Unknown |
| Curated By | Autocuration |
Publication
Imidazole derivatives as new potent and selective 20-HETE synthase inhibitors.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 12 | 8.05 | 8.96 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL262968 | — | — | 1 | 8.96 |
| CHEMBL113227 | — | — | 1 | 8.96 |
| CHEMBL115876 | — | — | 1 | 8.68 |
| CHEMBL113275 | — | — | 1 | 8.66 |
| CHEMBL112532 | — | — | 1 | 8.24 |
| CHEMBL320105 | — | — | 1 | 8.11 |
| CHEMBL113018 | — | — | 1 | 8.07 |
| CHEMBL267865 | — | — | 1 | 8.05 |
| CHEMBL114555 | — | — | 1 | 7.80 |
| CHEMBL112592 | — | — | 1 | 7.35 |
| CHEMBL114297 | — | — | 1 | 7.29 |
| CHEMBL325429 | — | — | 1 | 6.41 |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL262968 | — | IC50 | = | 1.1 | nM | 8.96 |
| CHEMBL113227 | — | IC50 | = | 1.1 | nM | 8.96 |
| CHEMBL115876 | — | IC50 | = | 2.1 | nM | 8.68 |
| CHEMBL113275 | — | IC50 | = | 2.2 | nM | 8.66 |
| CHEMBL112532 | — | IC50 | = | 5.7 | nM | 8.24 |
| CHEMBL320105 | — | IC50 | = | 7.7 | nM | 8.11 |
| CHEMBL113018 | — | IC50 | = | 8.6 | nM | 8.07 |
| CHEMBL267865 | — | IC50 | = | 8.9 | nM | 8.05 |
| CHEMBL114555 | — | IC50 | = | 16.0 | nM | 7.80 |
| CHEMBL112592 | — | IC50 | = | 45.0 | nM | 7.35 |
| CHEMBL114297 | — | IC50 | = | 51.0 | nM | 7.29 |
| CHEMBL325429 | — | IC50 | = | 387.0 | nM | 6.41 |