Assay Detail
Functional
CHEMBL891428
Review assay metadata, readout intent, target linkage, and publication context from the same page.
Antiviral activity against HIV1 RT 103N/181C mutant assessed as inhibition of viral-induced cytopathicity in MT4 cells by MTT method
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Functional |
| Organism | Human immunodeficiency virus 1 |
| Cell Type | MT4 |
| Confidence | 1 — Organism |
| Curated By | Intermediate |
Target
Human immunodeficiency virus 1 (CHEMBL378) ↗| Type | ORGANISM |
| Organism | Human immunodeficiency virus 1 |
Publication
Structure-activity relationship in the 3-iodo-4-phenoxypyridinone (IOPY) series: The nature of the C-3 substituent on anti-HIV activity.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 7 | 6.84 | 7.50 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL233452 | — | — | 1 | 7.50 |
| CHEMBL223228 | EFAVIRENZ | 4.0 | 1 | 7.40 |
| CHEMBL233664 | — | — | 1 | 7.40 |
| CHEMBL234077 | — | — | 1 | 6.80 |
| CHEMBL234283 | — | — | 1 | 6.70 |
| CHEMBL233662 | — | — | 1 | 6.30 |
| CHEMBL233453 | — | — | 1 | 5.80 |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL233452 | — | IC50 | = | 31.6 | nM | 7.50 |
| CHEMBL223228 | EFAVIRENZ | IC50 | = | 39.8 | nM | 7.40 |
| CHEMBL233664 | — | IC50 | = | 39.8 | nM | 7.40 |
| CHEMBL234077 | — | IC50 | = | 158.0 | nM | 6.80 |
| CHEMBL234283 | — | IC50 | = | 200.0 | nM | 6.70 |
| CHEMBL233662 | — | IC50 | = | 501.0 | nM | 6.30 |
| CHEMBL233453 | — | IC50 | = | 1584.0 | nM | 5.80 |