Assay Detail
Binding
CHEMBL982905
Review assay metadata, readout intent, target linkage, and publication context from the same page.
Inhibition of HIV1 recombinant protease M46I/A71V/V82T/I84V mutant expressed in Escherichia coli by spectrophotometric assay
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Binding |
| Organism | Human immunodeficiency virus 1 |
| Confidence | 9 — Direct single protein target |
| Curated By | Autocuration |
Target
Human immunodeficiency virus type 1 protease (CHEMBL243) ↗| Type | SINGLE PROTEIN |
| Organism | Human immunodeficiency virus 1 |
Publication
Inorganic polyhedral metallacarborane inhibitors of HIV protease: a new approach to overcoming antiviral resistance.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| Ki | 7 | 9.03 | 10.54 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL729 | LOPINAVIR | 4.0 | 1 | 10.54 |
| CHEMBL1323 | DARUNAVIR | 4.0 | 1 | 10.49 |
| CHEMBL1163 | ATAZANAVIR | 4.0 | 1 | 9.12 |
| CHEMBL116 | AMPRENAVIR | 4.0 | 1 | 9.05 |
| CHEMBL584 | NELFINAVIR | 4.0 | 1 | 8.42 |
| CHEMBL114 | SAQUINAVIR | 4.0 | 1 | 7.89 |
| CHEMBL5483011 | INDINAVIR | 3.0 | 1 | 7.68 |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL729 | LOPINAVIR | Ki | = | 0.029 | nM | 10.54 |
| CHEMBL1323 | DARUNAVIR | Ki | = | 0.032 | nM | 10.49 |
| CHEMBL1163 | ATAZANAVIR | Ki | = | 0.76 | nM | 9.12 |
| CHEMBL116 | AMPRENAVIR | Ki | = | 0.9 | nM | 9.05 |
| CHEMBL584 | NELFINAVIR | Ki | = | 3.8 | nM | 8.42 |
| CHEMBL114 | SAQUINAVIR | Ki | = | 13.0 | nM | 7.89 |
| CHEMBL5483011 | INDINAVIR | Ki | = | 21.0 | nM | 7.68 |