Assay Detail
Binding
CHEMBL5734847
Review assay metadata, readout intent, target linkage, and publication context from the same page.
TR-FRET Assay: Activity of the compounds was investigated using TACE (ADAM17) isolated enzyme. The screening of ADAM17 inhibitors was performed with a profluorescent peptidic substrate (Mca-Pro-Leu-Ala-Gln-Ala-Val-Dpa-Arg-Ser-Ser-Ser-Arg-NH2) which contains a highly fluorescent 7-methoxycoumarin (Mca) group that is efficiently quenched by resonance energy transfer to the 2,4-dinitrophenyl group (Dpa). Mca fluorescence was quenched by the Dpa group until cleavage by ADAM17 at the Ala-Val bond separates the two moieties.The enzymatic reaction was performed in 384-well microplates with a final volume of 10 uL containing 1% DMSO. Recombinant Human ADAM17 catalytic domain (500 nM) was assayed with 40 uM of substrate and serial dilutions of tested inhibitors (from 10000 nM to 0.04 nM). After two hours of incubation at room temperature, the fluorescence was measured using a microplate reader (320/425 nm).
27
Total Activities
9
Compounds Tested
3
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Binding |
| Organism | Homo sapiens |
| Confidence | 9 — Direct single protein target |
| Curated By | Autocuration |
Target
Disintegrin and metalloproteinase domain-containing protein 17 (CHEMBL3706) ↗| Type | SINGLE PROTEIN |
| Organism | Homo sapiens |
Publication
Benzenesulfonamide compounds, method for synthesizing same, and use thereof in medicine and cosmetics
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 9 | 8.23 | 8.55 |
| kon | 9 | - | - |
| k_off | 9 | - | - |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL5852735 | — | — | 3 | 8.55 |
| CHEMBL4209541 | — | — | 3 | 8.46 |
| CHEMBL4215407 | — | — | 3 | 8.43 |
| CHEMBL4210459 | — | — | 3 | 8.28 |
| CHEMBL5792040 | — | — | 3 | 8.25 |
| CHEMBL4208519 | — | — | 3 | 8.14 |
| CHEMBL6059811 | — | — | 3 | 8.09 |
| CHEMBL4206013 | — | — | 3 | 7.96 |
| CHEMBL5942356 | — | — | 3 | 7.94 |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL5852735 | — | IC50 | = | 2.8 | nM | 8.55 |
| CHEMBL4209541 | — | IC50 | = | 3.5 | nM | 8.46 |
| CHEMBL4215407 | — | IC50 | = | 3.7 | nM | 8.43 |
| CHEMBL4210459 | — | IC50 | = | 5.2 | nM | 8.28 |
| CHEMBL5792040 | — | IC50 | = | 5.6 | nM | 8.25 |
| CHEMBL4208519 | — | IC50 | = | 7.2 | nM | 8.14 |
| CHEMBL6059811 | — | IC50 | = | 8.2 | nM | 8.09 |
| CHEMBL4206013 | — | IC50 | = | 11.0 | nM | 7.96 |
| CHEMBL5942356 | — | IC50 | = | 11.4 | nM | 7.94 |
| CHEMBL4210459 | — | kon | = | - | — | - |
| CHEMBL4210459 | — | k_off | = | - | s-1 | - |
| CHEMBL5852735 | — | kon | = | - | — | - |
| CHEMBL5852735 | — | k_off | = | - | s-1 | - |
| CHEMBL6059811 | — | kon | = | - | — | - |
| CHEMBL6059811 | — | k_off | = | - | s-1 | - |
| CHEMBL4209541 | — | kon | = | - | — | - |
| CHEMBL4209541 | — | k_off | = | - | s-1 | - |
| CHEMBL4215407 | — | k_off | = | - | s-1 | - |
| CHEMBL4208519 | — | kon | = | - | — | - |
| CHEMBL5792040 | — | k_off | = | - | s-1 | - |
| CHEMBL5792040 | — | kon | = | - | — | - |
| CHEMBL5942356 | — | k_off | = | - | s-1 | - |
| CHEMBL5942356 | — | kon | = | - | — | - |
| CHEMBL4206013 | — | k_off | = | - | s-1 | - |
| CHEMBL4206013 | — | kon | = | - | — | - |
| CHEMBL4215407 | — | kon | = | - | — | - |
| CHEMBL4208519 | — | k_off | = | - | s-1 | - |