Assay Detail
Binding
CHEMBL880436
Review assay metadata, readout intent, target linkage, and publication context from the same page.
Inhibitory concentration against human dipeptidylpeptidase 8 using FP-TAMRA incubated for 30 min
12
Total Activities
12
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
Boro-norleucine as a P1 residue for the design of selective and potent DPP7 inhibitors.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 12 | 6.30 | 7.82 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL195189 | — | — | 1 | 7.82 |
| CHEMBL194852 | — | — | 1 | 7.52 |
| CHEMBL194428 | — | — | 1 | 7.02 |
| CHEMBL194250 | — | — | 1 | 6.72 |
| CHEMBL194517 | — | — | 1 | 6.46 |
| CHEMBL195271 | — | — | 1 | 6.40 |
| CHEMBL365322 | — | — | 1 | 6.17 |
| CHEMBL194249 | — | — | 1 | 6.00 |
| CHEMBL373319 | — | — | 1 | 5.58 |
| CHEMBL194354 | — | — | 1 | 5.37 |
| CHEMBL196180 | — | — | 1 | 5.28 |
| CHEMBL195481 | — | — | 1 | 5.22 |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL195189 | — | IC50 | = | 15.0 | nM | 7.82 |
| CHEMBL194852 | — | IC50 | = | 30.0 | nM | 7.52 |
| CHEMBL194428 | — | IC50 | = | 95.0 | nM | 7.02 |
| CHEMBL194250 | — | IC50 | = | 190.0 | nM | 6.72 |
| CHEMBL194517 | — | IC50 | = | 350.0 | nM | 6.46 |
| CHEMBL195271 | — | IC50 | = | 400.0 | nM | 6.40 |
| CHEMBL365322 | — | IC50 | = | 670.0 | nM | 6.17 |
| CHEMBL194249 | — | IC50 | = | 1000.0 | nM | 6.00 |
| CHEMBL373319 | — | IC50 | = | 2600.0 | nM | 5.58 |
| CHEMBL194354 | — | IC50 | = | 4300.0 | nM | 5.37 |
| CHEMBL196180 | — | IC50 | = | 5200.0 | nM | 5.28 |
| CHEMBL195481 | — | IC50 | = | 6000.0 | nM | 5.22 |