Assay Detail
Binding
CHEMBL656568
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Inhibition of human erythrocyte carbonic anhydrase II
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Binding |
| Confidence | 8 — Homologous single protein target |
| Curated By | Expert |
Publication
Thieno[2,3-b]furan-2-sulfonamides as topical carbonic anhydrase inhibitors.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 14 | 8.06 | 8.29 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL103143 | — | — | 1 | 8.29 |
| CHEMBL105080 | — | — | 1 | 8.25 |
| CHEMBL105713 | — | — | 1 | 8.22 |
| CHEMBL103255 | — | — | 1 | 8.19 |
| CHEMBL103271 | — | — | 1 | 8.10 |
| CHEMBL322014 | — | — | 1 | 8.10 |
| CHEMBL101371 | — | — | 1 | 8.09 |
| CHEMBL103087 | — | — | 1 | 8.05 |
| CHEMBL103621 | — | — | 1 | 7.96 |
| CHEMBL317694 | — | — | 1 | 7.96 |
| CHEMBL316757 | — | — | 1 | 7.96 |
| CHEMBL106493 | — | — | 1 | 7.92 |
| CHEMBL101370 | — | — | 1 | 7.92 |
| CHEMBL101792 | — | — | 1 | 7.85 |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL103143 | — | IC50 | = | 5.1 | nM | 8.29 |
| CHEMBL105080 | — | IC50 | = | 5.6 | nM | 8.25 |
| CHEMBL105713 | — | IC50 | = | 6.0 | nM | 8.22 |
| CHEMBL103255 | — | IC50 | = | 6.49 | nM | 8.19 |
| CHEMBL103271 | — | IC50 | = | 8.0 | nM | 8.10 |
| CHEMBL322014 | — | IC50 | = | 8.0 | nM | 8.10 |
| CHEMBL101371 | — | IC50 | = | 8.2 | nM | 8.09 |
| CHEMBL103087 | — | IC50 | = | 9.0 | nM | 8.05 |
| CHEMBL103621 | — | IC50 | = | 11.0 | nM | 7.96 |
| CHEMBL317694 | — | IC50 | = | 11.0 | nM | 7.96 |
| CHEMBL316757 | — | IC50 | = | 11.0 | nM | 7.96 |
| CHEMBL106493 | — | IC50 | = | 12.0 | nM | 7.92 |
| CHEMBL101370 | — | IC50 | = | 12.0 | nM | 7.92 |
| CHEMBL101792 | — | IC50 | = | 14.0 | nM | 7.85 |