Assay Detail
Binding
CHEMBL935616
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Inhibition of human full length carbonic anhydrase 7 by stopped flow CO2 hydrase assay
7
Total Activities
7
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
Carbonic anhydrase inhibitors: the X-ray crystal structure of ethoxzolamide complexed to human isoform II reveals the importance of thr200 and gln92 for obtaining tight-binding inhibitors.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| Ki | 7 | 8.38 | 9.10 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL18 | ETHOXZOLAMIDE | 4.0 | 1 | 9.10 |
| CHEMBL19 | METHAZOLAMIDE | 4.0 | 1 | 8.68 |
| CHEMBL20 | ACETAZOLAMIDE | 4.0 | 1 | 8.60 |
| CHEMBL220491 | BRINZOLAMIDE | 4.0 | 1 | 8.55 |
| CHEMBL218490 | DORZOLAMIDE | 4.0 | 1 | 8.46 |
| CHEMBL17 | DICHLORPHENAMIDE | 4.0 | 1 | 8.22 |
| CHEMBL262628 | — | — | 1 | 7.05 |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL18 | ETHOXZOLAMIDE | Ki | = | 0.8 | nM | 9.10 |
| CHEMBL19 | METHAZOLAMIDE | Ki | = | 2.1 | nM | 8.68 |
| CHEMBL20 | ACETAZOLAMIDE | Ki | = | 2.5 | nM | 8.60 |
| CHEMBL220491 | BRINZOLAMIDE | Ki | = | 2.8 | nM | 8.55 |
| CHEMBL218490 | DORZOLAMIDE | Ki | = | 3.5 | nM | 8.46 |
| CHEMBL17 | DICHLORPHENAMIDE | Ki | = | 6.0 | nM | 8.22 |
| CHEMBL262628 | — | Ki | = | 89.0 | nM | 7.05 |