Assay Detail
Functional
CHEMBL697155
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In vitro inhibition of human platelet aggregation induced by thromboxane mimetic U-46,619 (at a concentration of 0.3 uM)
10
Total Activities
10
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Functional |
| Organism | Homo sapiens |
| Confidence | 1 — Organism |
| Curated By | Intermediate |
Publication
Thrombin receptor (PAR-1) antagonists. Solid-phase synthesis of indole-based peptide mimetics by anchoring to a secondary amide.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 10 | 4.49 | 4.90 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL63402 | — | — | 1 | 4.90 |
| CHEMBL293867 | — | — | 1 | 4.67 |
| CHEMBL303157 | — | — | 1 | 4.58 |
| CHEMBL303187 | — | — | 1 | 4.48 |
| CHEMBL304829 | — | — | 1 | 4.44 |
| CHEMBL68458 | — | — | 1 | 4.40 |
| CHEMBL63966 | — | — | 1 | 4.38 |
| CHEMBL62775 | — | — | 1 | 4.36 |
| CHEMBL302603 | — | — | 1 | 4.36 |
| CHEMBL431369 | — | — | 1 | 4.35 |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL63402 | — | IC50 | = | 12500.0 | nM | 4.90 |
| CHEMBL293867 | — | IC50 | = | 21400.0 | nM | 4.67 |
| CHEMBL303157 | — | IC50 | = | 26200.0 | nM | 4.58 |
| CHEMBL303187 | — | IC50 | = | 33000.0 | nM | 4.48 |
| CHEMBL304829 | — | IC50 | = | 36300.0 | nM | 4.44 |
| CHEMBL68458 | — | IC50 | = | 39500.0 | nM | 4.40 |
| CHEMBL63966 | — | IC50 | = | 41900.0 | nM | 4.38 |
| CHEMBL62775 | — | IC50 | = | 44200.0 | nM | 4.36 |
| CHEMBL302603 | — | IC50 | = | 43500.0 | nM | 4.36 |
| CHEMBL431369 | — | IC50 | = | 44400.0 | nM | 4.35 |