Assay Detail
Functional
CHEMBL1959555
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Cytotoxicity against human primary leukemia cells isolated from acute myeloid leukemia patient expressing FLT3-ITD mutation assessed as cell viability after 72 hrs by luciferase assay
10
Total Activities
10
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Functional |
| Organism | Homo sapiens |
| Cell Type | Leukemia cell |
| Confidence | 1 — Organism |
| Curated By | Autocuration |
Publication
VX-322: a novel dual receptor tyrosine kinase inhibitor for the treatment of acute myelogenous leukemia.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 10 | 7.20 | 8.40 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL1835867 | — | — | 1 | 8.40 |
| CHEMBL1835870 | — | — | 1 | 7.92 |
| CHEMBL1835749 | — | — | 1 | 7.52 |
| CHEMBL1835747 | — | — | 1 | 7.52 |
| CHEMBL535 | SUNITINIB | 4.0 | 1 | 7.52 |
| CHEMBL1835746 | — | — | 1 | 7.05 |
| CHEMBL124660 | TANDUTINIB | 2.0 | 1 | 6.54 |
| CHEMBL1835743 | — | — | 1 | 6.39 |
| CHEMBL1833992 | — | — | 1 | 5.96 |
| CHEMBL941 | IMATINIB | 4.0 | 1 | - |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL1835867 | — | IC50 | = | 4.0 | nM | 8.40 |
| CHEMBL1835870 | — | IC50 | = | 12.0 | nM | 7.92 |
| CHEMBL1835749 | — | IC50 | = | 30.0 | nM | 7.52 |
| CHEMBL1835747 | — | IC50 | = | 30.0 | nM | 7.52 |
| CHEMBL535 | SUNITINIB | IC50 | = | 30.0 | nM | 7.52 |
| CHEMBL1835746 | — | IC50 | = | 90.0 | nM | 7.05 |
| CHEMBL124660 | TANDUTINIB | IC50 | = | 290.0 | nM | 6.54 |
| CHEMBL1835743 | — | IC50 | = | 410.0 | nM | 6.39 |
| CHEMBL1833992 | — | IC50 | = | 1100.0 | nM | 5.96 |
| CHEMBL941 | IMATINIB | IC50 | - | — | - |