Assay Detail
Functional
CHEMBL3620486
Review assay metadata, readout intent, target linkage, and publication context from the same page.
Cytotoxicity against human MDA-MB-231 cells assessed as cell viability after 5 days by cell viability analyzer
22
Total Activities
22
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Functional |
| Organism | Homo sapiens |
| Cell Type | MDA-MB-231 |
| Confidence | 1 — Organism |
| Curated By | Autocuration |
Publication
Design and synthesis of novel hydroxyanthraquinone nitrogen mustard derivatives as potential anticancer agents via a bioisostere approach.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 22 | 7.26 | 9.38 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL53463 | DOXORUBICIN | 4.0 | 1 | 9.38 |
| CHEMBL3617760 | — | — | 1 | 9.23 |
| CHEMBL3617860 | — | — | 1 | 8.67 |
| CHEMBL3617862 | — | — | 1 | 7.89 |
| CHEMBL3617757 | — | — | 1 | 7.84 |
| CHEMBL3617863 | — | — | 1 | 7.65 |
| CHEMBL3617763 | — | — | 1 | 7.32 |
| CHEMBL3617758 | — | — | 1 | 7.29 |
| CHEMBL3617761 | — | — | 1 | 7.22 |
| CHEMBL3617755 | — | — | 1 | 7.21 |
| CHEMBL3617756 | — | — | 1 | 7.11 |
| CHEMBL3617762 | — | — | 1 | 7.09 |
| CHEMBL3617754 | — | — | 1 | 7.07 |
| CHEMBL3617861 | — | — | 1 | 7.04 |
| CHEMBL3617759 | — | — | 1 | 6.86 |
| CHEMBL3617753 | — | — | 1 | 6.68 |
| CHEMBL3617866 | — | — | 1 | 6.56 |
| CHEMBL3617859 | — | — | 1 | 6.52 |
| CHEMBL3617865 | — | — | 1 | 6.50 |
| CHEMBL3617864 | — | — | 1 | 6.41 |
| CHEMBL515 | CHLORAMBUCIL | 4.0 | 1 | 6.28 |
| CHEMBL3616490 | — | — | 1 | 6.00 |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL53463 | DOXORUBICIN | IC50 | = | 0.414 | nM | 9.38 |
| CHEMBL3617760 | — | IC50 | = | 0.59 | nM | 9.23 |
| CHEMBL3617860 | — | IC50 | = | 2.13 | nM | 8.67 |
| CHEMBL3617862 | — | IC50 | = | 12.9 | nM | 7.89 |
| CHEMBL3617757 | — | IC50 | = | 14.6 | nM | 7.84 |
| CHEMBL3617863 | — | IC50 | = | 22.5 | nM | 7.65 |
| CHEMBL3617763 | — | IC50 | = | 48.0 | nM | 7.32 |
| CHEMBL3617758 | — | IC50 | = | 51.1 | nM | 7.29 |
| CHEMBL3617761 | — | IC50 | = | 59.6 | nM | 7.22 |
| CHEMBL3617755 | — | IC50 | = | 61.9 | nM | 7.21 |
| CHEMBL3617756 | — | IC50 | = | 77.6 | nM | 7.11 |
| CHEMBL3617762 | — | IC50 | = | 80.7 | nM | 7.09 |
| CHEMBL3617754 | — | IC50 | = | 84.5 | nM | 7.07 |
| CHEMBL3617861 | — | IC50 | = | 91.2 | nM | 7.04 |
| CHEMBL3617759 | — | IC50 | = | 137.0 | nM | 6.86 |
| CHEMBL3617753 | — | IC50 | = | 211.0 | nM | 6.68 |
| CHEMBL3617866 | — | IC50 | = | 278.0 | nM | 6.56 |
| CHEMBL3617859 | — | IC50 | = | 299.0 | nM | 6.52 |
| CHEMBL3617865 | — | IC50 | = | 316.0 | nM | 6.50 |
| CHEMBL3617864 | — | IC50 | = | 389.0 | nM | 6.41 |
| CHEMBL515 | CHLORAMBUCIL | IC50 | = | 520.0 | nM | 6.28 |
| CHEMBL3616490 | — | IC50 | = | 1000.0 | nM | 6.00 |