Assay Detail
Functional
CHEMBL4028769
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Cytotoxicity against human PC3 cells after 72 hrs by MTS assay
4
Total Activities
4
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Functional |
| Organism | Homo sapiens |
| Cell Type | PC-3 |
| Confidence | 1 — Organism |
| Curated By | Autocuration |
Publication
Heterocyclic-Fused Pyrimidines as Novel Tubulin Polymerization Inhibitors Targeting the Colchicine Binding Site: Structural Basis and Antitumor Efficacy.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 4 | 8.43 | 9.30 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL92 | DOCETAXEL ANHYDROUS | 4.0 | 1 | 9.30 |
| CHEMBL428647 | PACLITAXEL | 4.0 | 1 | 8.43 |
| CHEMBL107 | COLCHICINE | 4.0 | 1 | 8.10 |
| CHEMBL4102788 | — | — | 1 | 7.90 |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL92 | DOCETAXEL ANHYDROUS | IC50 | = | 0.5 | nM | 9.30 |
| CHEMBL428647 | PACLITAXEL | IC50 | = | 3.7 | nM | 8.43 |
| CHEMBL107 | COLCHICINE | IC50 | = | 8.0 | nM | 8.10 |
| CHEMBL4102788 | — | IC50 | = | 12.7 | nM | 7.90 |