Assay Detail
Binding
CHEMBL759073
Review assay metadata, readout intent, target linkage, and publication context from the same page.
Inhibition of protein kinase C delta
10
Total Activities
8
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
Potent and selective PKC inhibitory 5-membered ring analogs of balanol with replacement of the carboxamide moiety
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 10 | 7.89 | 9.00 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL48636 | — | — | 1 | 9.00 |
| CHEMBL300422 | — | — | 1 | 8.30 |
| CHEMBL295806 | — | — | 2 | 8.30 |
| CHEMBL265559 | — | — | 1 | 8.30 |
| CHEMBL49354 | — | — | 2 | 7.80 |
| CHEMBL48988 | — | — | 1 | 7.70 |
| CHEMBL48665 | — | — | 1 | 7.30 |
| CHEMBL48546 | — | — | 1 | 7.00 |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL48636 | — | IC50 | = | 1.0 | nM | 9.00 |
| CHEMBL300422 | — | IC50 | = | 5.0 | nM | 8.30 |
| CHEMBL295806 | — | IC50 | = | 5.0 | nM | 8.30 |
| CHEMBL265559 | — | IC50 | = | 5.0 | nM | 8.30 |
| CHEMBL49354 | — | IC50 | = | 16.0 | nM | 7.80 |
| CHEMBL48988 | — | IC50 | = | 20.0 | nM | 7.70 |
| CHEMBL49354 | — | IC50 | = | 23.0 | nM | 7.64 |
| CHEMBL295806 | — | IC50 | = | 30.0 | nM | 7.52 |
| CHEMBL48665 | — | IC50 | = | 50.0 | nM | 7.30 |
| CHEMBL48546 | — | IC50 | = | 100.0 | nM | 7.00 |