Assay Detail
Functional
CHEMBL1932094
Review assay metadata, readout intent, target linkage, and publication context from the same page.
Antiviral activity against wild type HIV1 NL4-3 infected in human TZM-bl cells after 48 hrs by luciferase reporter gene assay
20
Total Activities
20
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Functional |
| Organism | Human immunodeficiency virus 1 |
| Cell Type | TZM-bl |
| Confidence | 1 — Organism |
| Curated By | Autocuration |
Target
Human immunodeficiency virus 1 (CHEMBL378) ↗| Type | ORGANISM |
| Organism | Human immunodeficiency virus 1 |
Publication
Anti-AIDS agents 85. Design, synthesis, and evaluation of 1R,2R-dicamphanoyl-3,3-dimethyldihydropyrano-[2,3-c]xanthen-7(1H)-one (DCX) derivatives as novel anti-HIV agents.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| EC50 | 20 | 6.61 | 7.21 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL1928612 | — | — | 1 | 7.21 |
| CHEMBL1928440 | — | — | 1 | 7.20 |
| CHEMBL1928444 | — | — | 1 | 7.19 |
| CHEMBL435294 | — | — | 1 | 7.05 |
| CHEMBL1928443 | — | — | 1 | 7.02 |
| CHEMBL1928611 | — | — | 1 | 7.00 |
| CHEMBL1928447 | — | — | 1 | 6.92 |
| CHEMBL1928441 | — | — | 1 | 6.92 |
| CHEMBL1928449 | — | — | 1 | 6.85 |
| CHEMBL1928445 | — | — | 1 | 6.82 |
| CHEMBL1928438 | — | — | 1 | 6.70 |
| CHEMBL1928451 | — | — | 1 | 6.64 |
| CHEMBL1928439 | — | — | 1 | 6.54 |
| CHEMBL1928615 | — | — | 1 | 6.51 |
| CHEMBL1928450 | — | — | 1 | 6.48 |
| CHEMBL1928446 | — | — | 1 | 6.44 |
| CHEMBL1928613 | — | — | 1 | 5.83 |
| CHEMBL1928442 | — | — | 1 | 5.82 |
| CHEMBL1928448 | — | — | 1 | 5.77 |
| CHEMBL1928614 | — | — | 1 | 5.34 |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL1928612 | — | EC50 | = | 62.0 | nM | 7.21 |
| CHEMBL1928440 | — | EC50 | = | 63.0 | nM | 7.20 |
| CHEMBL1928444 | — | EC50 | = | 65.0 | nM | 7.19 |
| CHEMBL435294 | — | EC50 | = | 89.0 | nM | 7.05 |
| CHEMBL1928443 | — | EC50 | = | 95.0 | nM | 7.02 |
| CHEMBL1928611 | — | EC50 | = | 100.0 | nM | 7.00 |
| CHEMBL1928447 | — | EC50 | = | 120.0 | nM | 6.92 |
| CHEMBL1928441 | — | EC50 | = | 120.0 | nM | 6.92 |
| CHEMBL1928449 | — | EC50 | = | 140.0 | nM | 6.85 |
| CHEMBL1928445 | — | EC50 | = | 150.0 | nM | 6.82 |
| CHEMBL1928438 | — | EC50 | = | 200.0 | nM | 6.70 |
| CHEMBL1928451 | — | EC50 | = | 230.0 | nM | 6.64 |
| CHEMBL1928439 | — | EC50 | = | 290.0 | nM | 6.54 |
| CHEMBL1928615 | — | EC50 | = | 308.0 | nM | 6.51 |
| CHEMBL1928450 | — | EC50 | = | 330.0 | nM | 6.48 |
| CHEMBL1928446 | — | EC50 | = | 362.0 | nM | 6.44 |
| CHEMBL1928613 | — | EC50 | = | 1470.0 | nM | 5.83 |
| CHEMBL1928442 | — | EC50 | = | 1520.0 | nM | 5.82 |
| CHEMBL1928448 | — | EC50 | = | 1700.0 | nM | 5.77 |
| CHEMBL1928614 | — | EC50 | = | 4530.0 | nM | 5.34 |