Assay Detail
Functional
CHEMBL1042767
Review assay metadata, readout intent, target linkage, and publication context from the same page.
Antiviral activity against HIV1 3B infected in human HOS cells
28
Total Activities
28
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Functional |
| Organism | Human immunodeficiency virus 1 |
| Cell Type | HOS |
| Confidence | 1 — Organism |
| Curated By | Autocuration |
Target
Human immunodeficiency virus 1 (CHEMBL378) ↗| Type | ORGANISM |
| Organism | Human immunodeficiency virus 1 |
Publication
Amine substituted N-(1H-benzimidazol-2ylmethyl)-5,6,7,8-tetrahydro-8-quinolinamines as CXCR4 antagonists with potent activity against HIV-1.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 28 | 7.34 | 9.22 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL570532 | — | — | 1 | 9.22 |
| CHEMBL568653 | — | — | 1 | 8.70 |
| CHEMBL568652 | — | — | 1 | 8.22 |
| CHEMBL584896 | — | — | 1 | 8.16 |
| CHEMBL518924 | MAVORIXAFOR | 4.0 | 1 | 8.00 |
| CHEMBL583443 | — | — | 1 | 7.89 |
| CHEMBL568447 | — | — | 1 | 7.77 |
| CHEMBL565749 | — | — | 1 | 7.72 |
| CHEMBL576429 | — | — | 1 | 7.66 |
| CHEMBL578570 | — | — | 1 | 7.64 |
| CHEMBL577021 | — | — | 1 | 7.62 |
| CHEMBL568661 | — | — | 1 | 7.60 |
| CHEMBL584075 | — | — | 1 | 7.58 |
| CHEMBL577255 | — | — | 1 | 7.57 |
| CHEMBL577486 | — | — | 1 | 7.48 |
| CHEMBL568660 | — | — | 1 | 7.39 |
| CHEMBL577268 | — | — | 1 | 7.36 |
| CHEMBL578989 | — | — | 1 | 7.34 |
| CHEMBL576427 | — | — | 1 | 6.87 |
| CHEMBL568233 | — | — | 1 | 6.84 |
| CHEMBL585750 | — | — | 1 | 6.71 |
| CHEMBL585565 | — | — | 1 | 6.64 |
| CHEMBL568234 | — | — | 1 | 6.61 |
| CHEMBL565544 | — | — | 1 | 6.57 |
| CHEMBL568245 | — | — | 1 | 6.40 |
| CHEMBL568442 | — | — | 1 | 6.27 |
| CHEMBL567586 | — | — | 1 | 5.89 |
| CHEMBL565978 | — | — | 1 | 5.87 |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL570532 | — | IC50 | = | 0.6 | nM | 9.22 |
| CHEMBL568653 | — | IC50 | = | 2.0 | nM | 8.70 |
| CHEMBL568652 | — | IC50 | = | 6.0 | nM | 8.22 |
| CHEMBL584896 | — | IC50 | = | 6.9 | nM | 8.16 |
| CHEMBL518924 | MAVORIXAFOR | IC50 | = | 10.0 | nM | 8.00 |
| CHEMBL583443 | — | IC50 | = | 13.0 | nM | 7.89 |
| CHEMBL568447 | — | IC50 | = | 17.0 | nM | 7.77 |
| CHEMBL565749 | — | IC50 | = | 19.0 | nM | 7.72 |
| CHEMBL576429 | — | IC50 | = | 22.0 | nM | 7.66 |
| CHEMBL578570 | — | IC50 | = | 23.0 | nM | 7.64 |
| CHEMBL577021 | — | IC50 | = | 24.0 | nM | 7.62 |
| CHEMBL568661 | — | IC50 | = | 25.0 | nM | 7.60 |
| CHEMBL584075 | — | IC50 | = | 26.0 | nM | 7.58 |
| CHEMBL577255 | — | IC50 | = | 27.0 | nM | 7.57 |
| CHEMBL577486 | — | IC50 | = | 33.0 | nM | 7.48 |
| CHEMBL568660 | — | IC50 | = | 41.0 | nM | 7.39 |
| CHEMBL577268 | — | IC50 | = | 44.0 | nM | 7.36 |
| CHEMBL578989 | — | IC50 | = | 46.0 | nM | 7.34 |
| CHEMBL576427 | — | IC50 | = | 134.0 | nM | 6.87 |
| CHEMBL568233 | — | IC50 | = | 144.0 | nM | 6.84 |
| CHEMBL585750 | — | IC50 | = | 197.0 | nM | 6.71 |
| CHEMBL585565 | — | IC50 | = | 228.0 | nM | 6.64 |
| CHEMBL568234 | — | IC50 | = | 243.0 | nM | 6.61 |
| CHEMBL565544 | — | IC50 | = | 271.0 | nM | 6.57 |
| CHEMBL568245 | — | IC50 | = | 396.0 | nM | 6.40 |
| CHEMBL568442 | — | IC50 | = | 540.0 | nM | 6.27 |
| CHEMBL567586 | — | IC50 | = | 1300.0 | nM | 5.89 |
| CHEMBL565978 | — | IC50 | = | 1350.0 | nM | 5.87 |