Assay Detail
Binding
CHEMBL713992
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Inhibition of human matrix metalloprotease 1
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Binding |
| Organism | Homo sapiens |
| Confidence | 9 — Direct single protein target |
| Curated By | Expert |
Publication
Design and synthesis of phosphinamide-based hydroxamic acids as inhibitors of matrix metalloproteinases.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 13 | 6.09 | 7.69 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL176602 | — | — | 1 | 7.69 |
| CHEMBL514138 | CGS-27023A | — | 1 | 7.30 |
| CHEMBL355752 | — | — | 1 | 6.92 |
| CHEMBL367420 | — | — | 1 | 6.29 |
| CHEMBL353479 | — | — | 1 | 6.28 |
| CHEMBL172857 | — | — | 1 | 6.22 |
| CHEMBL173208 | — | — | 1 | 6.07 |
| CHEMBL174037 | — | — | 1 | 5.89 |
| CHEMBL367675 | — | — | 1 | 5.60 |
| CHEMBL173207 | — | — | 1 | 5.17 |
| CHEMBL368946 | — | — | 1 | 5.15 |
| CHEMBL366759 | — | — | 1 | 4.48 |
| CHEMBL355754 | — | — | 1 | - |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL176602 | — | IC50 | = | 20.5 | nM | 7.69 |
| CHEMBL514138 | CGS-27023A | IC50 | = | 49.5 | nM | 7.30 |
| CHEMBL355752 | — | IC50 | = | 120.0 | nM | 6.92 |
| CHEMBL367420 | — | IC50 | = | 518.0 | nM | 6.29 |
| CHEMBL353479 | — | IC50 | = | 525.0 | nM | 6.28 |
| CHEMBL172857 | — | IC50 | = | 608.0 | nM | 6.22 |
| CHEMBL173208 | — | IC50 | = | 854.0 | nM | 6.07 |
| CHEMBL174037 | — | IC50 | = | 1290.0 | nM | 5.89 |
| CHEMBL367675 | — | IC50 | = | 2510.0 | nM | 5.60 |
| CHEMBL173207 | — | IC50 | = | 6790.0 | nM | 5.17 |
| CHEMBL368946 | — | IC50 | = | 7120.0 | nM | 5.15 |
| CHEMBL366759 | — | IC50 | = | 33300.0 | nM | 4.48 |
| CHEMBL355754 | — | IC50 | > | 100000.0 | nM | - |