Assay Detail
Functional
CHEMBL3772616
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Antiproliferative activity against human HCT116 cells assessed as reduction in cell viability after 96 hrs by sulforhodamine B assay
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Functional |
| Organism | Homo sapiens |
| Cell Type | HCT-116 |
| Confidence | 1 — Organism |
| Curated By | Autocuration |
Publication
Synthesis and biological evaluation of D-ring fused 1,2,3-thiadiazole dehydroepiandrosterone derivatives as antitumor agents.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 7 | 5.23 | 5.70 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL3770137 | — | — | 1 | 5.70 |
| CHEMBL3771045 | — | — | 1 | 5.07 |
| CHEMBL3769913 | — | — | 1 | 4.93 |
| CHEMBL272195 | EPIANDROSTERONE | — | 1 | - |
| CHEMBL90593 | PRASTERONE | 4.0 | 1 | - |
| CHEMBL3769728 | — | — | 1 | - |
| CHEMBL3770683 | — | — | 1 | - |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL3770137 | — | IC50 | = | 2010.0 | nM | 5.70 |
| CHEMBL3771045 | — | IC50 | = | 8520.0 | nM | 5.07 |
| CHEMBL3769913 | — | IC50 | = | 11700.0 | nM | 4.93 |
| CHEMBL272195 | EPIANDROSTERONE | IC50 | > | 50000.0 | nM | - |
| CHEMBL90593 | PRASTERONE | IC50 | > | 50000.0 | nM | - |
| CHEMBL3769728 | — | IC50 | > | 50000.0 | nM | - |
| CHEMBL3770683 | — | IC50 | > | 50000.0 | nM | - |