Assay Detail
Functional
CHEMBL864456
Review assay metadata, readout intent, target linkage, and publication context from the same page.
Antiviral activity against HIV1 IRLL98 mutant strain infected MT4 cells by MTT method
33
Total Activities
33
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 | Expert |
Target
Human immunodeficiency virus 1 (CHEMBL378) ↗| Type | ORGANISM |
| Organism | Human immunodeficiency virus 1 |
Publication
Parallel solution-phase and microwave-assisted synthesis of new S-DABO derivatives endowed with subnanomolar anti-HIV-1 activity.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| EC50 | 33 | 6.28 | 9.66 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL196807 | — | — | 1 | 9.66 |
| CHEMBL129 | ZIDOVUDINE | 4.0 | 1 | 8.10 |
| CHEMBL199234 | — | — | 1 | 7.33 |
| CHEMBL382737 | — | — | 1 | 6.96 |
| CHEMBL223228 | EFAVIRENZ | 4.0 | 1 | 6.70 |
| CHEMBL373030 | — | — | 1 | 6.29 |
| CHEMBL198702 | — | — | 1 | 6.16 |
| CHEMBL200477 | — | — | 1 | 6.03 |
| CHEMBL198465 | — | — | 1 | 6.00 |
| CHEMBL370996 | — | — | 1 | 5.72 |
| CHEMBL436507 | — | — | 1 | 5.68 |
| CHEMBL197881 | — | — | 1 | 5.66 |
| CHEMBL197125 | — | — | 1 | 5.57 |
| CHEMBL439863 | — | — | 1 | 5.48 |
| CHEMBL198704 | — | — | 1 | 5.32 |
| CHEMBL372381 | — | — | 1 | 5.30 |
| CHEMBL198805 | — | — | 1 | 4.80 |
| CHEMBL199223 | — | — | 1 | - |
| CHEMBL196756 | — | — | 1 | - |
| CHEMBL196811 | — | — | 1 | - |
| CHEMBL371251 | — | — | 1 | - |
| CHEMBL199113 | — | — | 1 | - |
| CHEMBL198697 | — | — | 1 | - |
| CHEMBL57 | NEVIRAPINE | 4.0 | 1 | - |
| CHEMBL198370 | — | — | 1 | - |
| CHEMBL197874 | — | — | 1 | - |
| CHEMBL410272 | — | — | 1 | - |
| CHEMBL196965 | — | — | 1 | - |
| CHEMBL199164 | — | — | 1 | - |
| CHEMBL200626 | — | — | 1 | - |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL196807 | — | EC50 | = | 0.22 | nM | 9.66 |
| CHEMBL129 | ZIDOVUDINE | EC50 | = | 8.0 | nM | 8.10 |
| CHEMBL199234 | — | EC50 | = | 47.0 | nM | 7.33 |
| CHEMBL382737 | — | EC50 | = | 110.0 | nM | 6.96 |
| CHEMBL223228 | EFAVIRENZ | EC50 | = | 200.0 | nM | 6.70 |
| CHEMBL373030 | — | EC50 | = | 510.0 | nM | 6.29 |
| CHEMBL198702 | — | EC50 | = | 690.0 | nM | 6.16 |
| CHEMBL200477 | — | EC50 | = | 930.0 | nM | 6.03 |
| CHEMBL198465 | — | EC50 | = | 1000.0 | nM | 6.00 |
| CHEMBL370996 | — | EC50 | = | 1900.0 | nM | 5.72 |
| CHEMBL436507 | — | EC50 | = | 2100.0 | nM | 5.68 |
| CHEMBL197881 | — | EC50 | = | 2200.0 | nM | 5.66 |
| CHEMBL197125 | — | EC50 | = | 2700.0 | nM | 5.57 |
| CHEMBL439863 | — | EC50 | = | 3300.0 | nM | 5.48 |
| CHEMBL198704 | — | EC50 | = | 4800.0 | nM | 5.32 |
| CHEMBL372381 | — | EC50 | = | 5000.0 | nM | 5.30 |
| CHEMBL198805 | — | EC50 | = | 16000.0 | nM | 4.80 |
| CHEMBL199223 | — | EC50 | > | 48000.0 | nM | - |
| CHEMBL196756 | — | EC50 | > | 8900.0 | nM | - |
| CHEMBL196811 | — | EC50 | > | 64000.0 | nM | - |
| CHEMBL371251 | — | EC50 | > | 2800.0 | nM | - |
| CHEMBL199113 | — | EC50 | > | 53000.0 | nM | - |
| CHEMBL198697 | — | EC50 | > | 50000.0 | nM | - |
| CHEMBL57 | NEVIRAPINE | EC50 | > | 7500.0 | nM | - |
| CHEMBL198370 | — | EC50 | > | 65000.0 | nM | - |
| CHEMBL197874 | — | EC50 | > | 60000.0 | nM | - |
| CHEMBL410272 | — | EC50 | > | 62000.0 | nM | - |
| CHEMBL196965 | — | EC50 | > | 65000.0 | nM | - |
| CHEMBL199164 | — | EC50 | > | 55000.0 | nM | - |
| CHEMBL200626 | — | EC50 | > | 55000.0 | nM | - |
| CHEMBL197343 | — | EC50 | > | 57000.0 | nM | - |
| CHEMBL199060 | — | EC50 | > | 41000.0 | nM | - |
| CHEMBL198193 | — | EC50 | > | 53000.0 | nM | - |