Assay Detail
Functional
CHEMBL2328539
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Inhibition of IL-2 production in human T cells measured after 2 to 3 days by ELISA
28
Total Activities
28
Compounds Tested
1
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Functional |
| Organism | Homo sapiens |
| Cell Type | T-cell |
| Confidence | 1 — Organism |
| Curated By | Autocuration |
Publication
Isosteric analogs of lenalidomide and pomalidomide: synthesis and biological activity.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| EC50 | 28 | 7.17 | 8.10 |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL43452 | POMALIDOMIDE | 4.0 | 1 | 8.10 |
| CHEMBL2324719 | — | — | 1 | 8.00 |
| CHEMBL2324705 | — | — | 1 | 7.68 |
| CHEMBL2324726 | — | — | 1 | 7.35 |
| CHEMBL2324715 | — | — | 1 | 7.24 |
| CHEMBL848 | LENALIDOMIDE | 4.0 | 1 | 6.82 |
| CHEMBL2324709 | — | — | 1 | 6.19 |
| CHEMBL2324725 | — | — | 1 | 5.96 |
| CHEMBL2324708 | — | — | 1 | - |
| CHEMBL468 | THALIDOMIDE | 4.0 | 1 | - |
| CHEMBL2324710 | — | — | 1 | - |
| CHEMBL2324711 | — | — | 1 | - |
| CHEMBL2324712 | — | — | 1 | - |
| CHEMBL2324713 | — | — | 1 | - |
| CHEMBL2324714 | — | — | 1 | - |
| CHEMBL2324716 | — | — | 1 | - |
| CHEMBL2324717 | — | — | 1 | - |
| CHEMBL2324718 | — | — | 1 | - |
| CHEMBL2324707 | — | — | 1 | - |
| CHEMBL2324704 | — | — | 1 | - |
| CHEMBL2324703 | — | — | 1 | - |
| CHEMBL2324702 | — | — | 1 | - |
| CHEMBL2324724 | — | — | 1 | - |
| CHEMBL2324723 | — | — | 1 | - |
| CHEMBL2324722 | — | — | 1 | - |
| CHEMBL2324721 | — | — | 1 | - |
| CHEMBL2324720 | — | — | 1 | - |
| CHEMBL2324706 | — | — | 1 | - |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL43452 | POMALIDOMIDE | EC50 | = | 8.0 | nM | 8.10 |
| CHEMBL2324719 | — | EC50 | = | 10.0 | nM | 8.00 |
| CHEMBL2324705 | — | EC50 | = | 21.0 | nM | 7.68 |
| CHEMBL2324726 | — | EC50 | = | 45.0 | nM | 7.35 |
| CHEMBL2324715 | — | EC50 | = | 57.0 | nM | 7.24 |
| CHEMBL848 | LENALIDOMIDE | EC50 | = | 150.0 | nM | 6.82 |
| CHEMBL2324709 | — | EC50 | = | 650.0 | nM | 6.19 |
| CHEMBL2324725 | — | EC50 | = | 1100.0 | nM | 5.96 |
| CHEMBL2324708 | — | EC50 | > | 1000.0 | nM | - |
| CHEMBL468 | THALIDOMIDE | EC50 | > | 10000.0 | nM | - |
| CHEMBL2324710 | — | EC50 | > | 1000.0 | nM | - |
| CHEMBL2324711 | — | EC50 | > | 1000.0 | nM | - |
| CHEMBL2324712 | — | EC50 | > | 1000.0 | nM | - |
| CHEMBL2324713 | — | EC50 | > | 1000.0 | nM | - |
| CHEMBL2324714 | — | EC50 | > | 1000.0 | nM | - |
| CHEMBL2324716 | — | EC50 | > | 1000.0 | nM | - |
| CHEMBL2324717 | — | EC50 | > | 1000.0 | nM | - |
| CHEMBL2324718 | — | EC50 | > | 10000.0 | nM | - |
| CHEMBL2324707 | — | EC50 | > | 1000.0 | nM | - |
| CHEMBL2324704 | — | EC50 | > | 1000.0 | nM | - |
| CHEMBL2324703 | — | EC50 | > | 1000.0 | nM | - |
| CHEMBL2324702 | — | EC50 | > | 1000.0 | nM | - |
| CHEMBL2324724 | — | EC50 | > | 10000.0 | nM | - |
| CHEMBL2324723 | — | EC50 | > | 10000.0 | nM | - |
| CHEMBL2324722 | — | EC50 | > | 10000.0 | nM | - |
| CHEMBL2324721 | — | EC50 | > | 10000.0 | nM | - |
| CHEMBL2324720 | — | EC50 | > | 10000.0 | nM | - |
| CHEMBL2324706 | — | EC50 | > | 1000.0 | nM | - |