Assay Detail
Functional
CHEMBL715739
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Anti-HIV activity to reduce HIV-1-induced cytopathic effect by 50% in MT-4 cells against HIV-1 IIIB
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Functional |
| Organism | Homo sapiens |
| Cell Type | MT4 |
| Confidence | 1 — Organism |
| Curated By | Intermediate |
Publication
Discovery of 2,3-diaryl-1,3-thiazolidin-4-ones as potent anti-HIV-1 agents.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| EC50 | 13 | 6.11 | 7.36 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL48427 | — | — | 1 | 7.36 |
| CHEMBL296589 | — | — | 1 | 7.09 |
| CHEMBL300179 | — | — | 1 | 6.83 |
| CHEMBL50805 | — | — | 1 | 6.75 |
| CHEMBL50019 | — | — | 1 | 6.61 |
| CHEMBL53554 | THIAZOLOBENZIMIDAZOLE | — | 1 | 6.45 |
| CHEMBL299364 | — | — | 1 | 6.40 |
| CHEMBL296175 | — | — | 1 | 6.23 |
| CHEMBL50948 | — | — | 1 | 6.07 |
| CHEMBL53540 | — | — | 1 | 5.29 |
| CHEMBL50428 | — | — | 1 | 4.27 |
| CHEMBL300859 | — | — | 1 | 4.02 |
| CHEMBL51254 | — | — | 1 | - |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL48427 | — | EC50 | = | 44.0 | nM | 7.36 |
| CHEMBL296589 | — | EC50 | = | 82.0 | nM | 7.09 |
| CHEMBL300179 | — | EC50 | = | 147.0 | nM | 6.83 |
| CHEMBL50805 | — | EC50 | = | 178.0 | nM | 6.75 |
| CHEMBL50019 | — | EC50 | = | 248.0 | nM | 6.61 |
| CHEMBL53554 | THIAZOLOBENZIMIDAZOLE | EC50 | = | 352.0 | nM | 6.45 |
| CHEMBL299364 | — | EC50 | = | 401.0 | nM | 6.40 |
| CHEMBL296175 | — | EC50 | = | 589.0 | nM | 6.23 |
| CHEMBL50948 | — | EC50 | = | 855.0 | nM | 6.07 |
| CHEMBL53540 | — | EC50 | = | 5130.0 | nM | 5.29 |
| CHEMBL50428 | — | EC50 | = | 53500.0 | nM | 4.27 |
| CHEMBL300859 | — | EC50 | = | 95100.0 | nM | 4.02 |
| CHEMBL51254 | — | EC50 | > | 23000.0 | nM | - |