Assay Detail
Functional
CHEMBL890376
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Antiviral activity against HIV1 LAI assessed as inhibition of viral-induced cytopathicity in MT4 cells by MTT method
28
Total Activities
28
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 | 28 | 7.54 | 9.00 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL223228 | EFAVIRENZ | 4.0 | 1 | 9.00 |
| CHEMBL233664 | — | — | 1 | 8.90 |
| CHEMBL234077 | — | — | 1 | 8.70 |
| CHEMBL233452 | — | — | 1 | 8.70 |
| CHEMBL233662 | — | — | 1 | 8.60 |
| CHEMBL234283 | — | — | 1 | 8.51 |
| CHEMBL395522 | — | — | 1 | 8.51 |
| CHEMBL233663 | — | — | 1 | 8.51 |
| CHEMBL234282 | — | — | 1 | 8.20 |
| CHEMBL234285 | — | — | 1 | 8.20 |
| CHEMBL233453 | — | — | 1 | 8.00 |
| CHEMBL234284 | — | — | 1 | 7.90 |
| CHEMBL395521 | — | — | 1 | 7.80 |
| CHEMBL397933 | — | — | 1 | 7.80 |
| CHEMBL233439 | — | — | 1 | 7.70 |
| CHEMBL397934 | — | — | 1 | 7.70 |
| CHEMBL232030 | — | — | 1 | 7.50 |
| CHEMBL233672 | — | — | 1 | 7.40 |
| CHEMBL397909 | — | — | 1 | 7.30 |
| CHEMBL388864 | — | — | 1 | 7.20 |
| CHEMBL233881 | — | — | 1 | 7.10 |
| CHEMBL388865 | — | — | 1 | 7.00 |
| CHEMBL233674 | — | — | 1 | 6.90 |
| CHEMBL231902 | — | — | 1 | 6.40 |
| CHEMBL388641 | — | — | 1 | 6.20 |
| CHEMBL233878 | — | — | 1 | 5.30 |
| CHEMBL388642 | — | — | 1 | 5.20 |
| CHEMBL233673 | — | — | 1 | 4.80 |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL223228 | EFAVIRENZ | IC50 | = | 1.0 | nM | 9.00 |
| CHEMBL233664 | — | IC50 | = | 1.25 | nM | 8.90 |
| CHEMBL234077 | — | IC50 | = | 1.99 | nM | 8.70 |
| CHEMBL233452 | — | IC50 | = | 1.99 | nM | 8.70 |
| CHEMBL233662 | — | IC50 | = | 2.5 | nM | 8.60 |
| CHEMBL234283 | — | IC50 | = | 3.1 | nM | 8.51 |
| CHEMBL395522 | — | IC50 | = | 3.1 | nM | 8.51 |
| CHEMBL233663 | — | IC50 | = | 3.1 | nM | 8.51 |
| CHEMBL234282 | — | IC50 | = | 6.3 | nM | 8.20 |
| CHEMBL234285 | — | IC50 | = | 6.3 | nM | 8.20 |
| CHEMBL233453 | — | IC50 | = | 10.0 | nM | 8.00 |
| CHEMBL234284 | — | IC50 | = | 12.5 | nM | 7.90 |
| CHEMBL395521 | — | IC50 | = | 15.8 | nM | 7.80 |
| CHEMBL397933 | — | IC50 | = | 15.8 | nM | 7.80 |
| CHEMBL233439 | — | IC50 | = | 19.9 | nM | 7.70 |
| CHEMBL397934 | — | IC50 | = | 19.9 | nM | 7.70 |
| CHEMBL232030 | — | IC50 | = | 31.6 | nM | 7.50 |
| CHEMBL233672 | — | IC50 | = | 39.8 | nM | 7.40 |
| CHEMBL397909 | — | IC50 | = | 50.1 | nM | 7.30 |
| CHEMBL388864 | — | IC50 | = | 63.1 | nM | 7.20 |
| CHEMBL233881 | — | IC50 | = | 79.4 | nM | 7.10 |
| CHEMBL388865 | — | IC50 | = | 100.0 | nM | 7.00 |
| CHEMBL233674 | — | IC50 | = | 125.0 | nM | 6.90 |
| CHEMBL231902 | — | IC50 | = | 398.0 | nM | 6.40 |
| CHEMBL388641 | — | IC50 | = | 631.0 | nM | 6.20 |
| CHEMBL233878 | — | IC50 | = | 5020.0 | nM | 5.30 |
| CHEMBL388642 | — | IC50 | = | 6310.0 | nM | 5.20 |
| CHEMBL233673 | — | IC50 | = | 15848.0 | nM | 4.80 |