Assay Detail
Binding
CHEMBL766685
Review assay metadata, readout intent, target linkage, and publication context from the same page.
Inhibition of Protein Kinase A
12
Total Activities
8
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Binding |
| Confidence | 4 — Cell-line / Tissue |
| Curated By | Autocuration |
Target
cAMP-dependent protein kinase (PKA) (CHEMBL2094138) ↗| Type | PROTEIN FAMILY |
| Organism | Homo sapiens |
Publication
Synthesis and biological evaluation of conformationally constrained bicyclic and tricyclic balanol analogues as inhibitors of protein kinase C
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 12 | 6.06 | 7.52 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL71331 | — | — | 1 | 7.52 |
| CHEMBL311399 | — | — | 1 | 7.22 |
| CHEMBL422056 | — | — | 1 | 7.16 |
| CHEMBL305667 | — | — | 2 | 5.72 |
| CHEMBL306884 | — | — | 2 | 5.70 |
| CHEMBL306170 | — | — | 1 | 4.58 |
| CHEMBL72480 | — | — | 2 | 4.50 |
| CHEMBL306883 | — | — | 2 | - |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL71331 | — | IC50 | = | 30.0 | nM | 7.52 |
| CHEMBL311399 | — | IC50 | = | 60.0 | nM | 7.22 |
| CHEMBL422056 | — | IC50 | = | 70.0 | nM | 7.16 |
| CHEMBL305667 | — | IC50 | = | 1900.0 | nM | 5.72 |
| CHEMBL306884 | — | IC50 | = | 2000.0 | nM | 5.70 |
| CHEMBL306170 | — | IC50 | = | 26000.0 | nM | 4.58 |
| CHEMBL72480 | — | IC50 | = | 32000.0 | nM | 4.50 |
| CHEMBL306883 | — | IC50 | > | 50000.0 | nM | - |
| CHEMBL305667 | — | IC50 | > | 50000.0 | nM | - |
| CHEMBL306884 | — | IC50 | > | 50000.0 | nM | - |
| CHEMBL72480 | — | IC50 | > | 50000.0 | nM | - |
| CHEMBL306883 | — | IC50 | > | 50000.0 | nM | - |