Assay Detail
Functional
CHEMBL701776
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Growth inhibitory activity against human Jurkat leukemia cell line (JLC)
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Functional |
| Organism | Homo sapiens |
| Cell Type | Jurkat |
| Confidence | 1 — Organism |
| Curated By | Intermediate |
Publication
Synthesis and cytotoxic activity of carboxamide derivatives of benzo[b][1,6]naphthyridines.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 13 | 7.44 | 9.00 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL9902 | — | — | 1 | 9.00 |
| CHEMBL65 | CAMPTOTHECIN | -1.0 | 1 | 8.25 |
| CHEMBL9676 | — | — | 1 | 8.17 |
| CHEMBL9595 | — | — | 1 | 8.07 |
| CHEMBL268798 | — | — | 1 | 8.03 |
| CHEMBL53463 | DOXORUBICIN | 4.0 | 1 | 8.02 |
| CHEMBL269663 | — | — | 1 | 7.58 |
| CHEMBL9489 | — | — | 1 | 7.29 |
| CHEMBL266809 | — | — | 1 | 6.91 |
| CHEMBL44657 | ETOPOSIDE | 4.0 | 1 | 6.80 |
| CHEMBL276261 | — | — | 1 | 6.37 |
| CHEMBL9940 | — | — | 1 | 6.24 |
| CHEMBL611408 | — | — | 1 | 5.97 |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL9902 | — | IC50 | = | 1.0 | nM | 9.00 |
| CHEMBL65 | CAMPTOTHECIN | IC50 | = | 5.6 | nM | 8.25 |
| CHEMBL9676 | — | IC50 | = | 6.7 | nM | 8.17 |
| CHEMBL9595 | — | IC50 | = | 8.5 | nM | 8.07 |
| CHEMBL268798 | — | IC50 | = | 9.4 | nM | 8.03 |
| CHEMBL53463 | DOXORUBICIN | IC50 | = | 9.6 | nM | 8.02 |
| CHEMBL269663 | — | IC50 | = | 26.0 | nM | 7.58 |
| CHEMBL9489 | — | IC50 | = | 51.0 | nM | 7.29 |
| CHEMBL266809 | — | IC50 | = | 123.0 | nM | 6.91 |
| CHEMBL44657 | ETOPOSIDE | IC50 | = | 160.0 | nM | 6.80 |
| CHEMBL276261 | — | IC50 | = | 424.0 | nM | 6.37 |
| CHEMBL9940 | — | IC50 | = | 580.0 | nM | 6.24 |
| CHEMBL611408 | — | IC50 | = | 1070.0 | nM | 5.97 |