Assay Detail
Binding
CHEMBL918699
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Inhibition of human recombinant DHFR
7
Total Activities
6
Compounds Tested
2
Activity Types
0
Assay Parameters
Assay Information
| Assay Type | Binding |
| Organism | Homo sapiens |
| Confidence | 9 — Direct single protein target |
| Curated By | Intermediate |
Publication
Synthesis of classical, three-carbon-bridged 5-substituted furo[2,3-d]pyrimidine and 6-substituted pyrrolo[2,3-d]pyrimidine analogues as antifolates.
Activity Statistics
| Type | Count | Avg pChEMBL | Best pChEMBL |
|---|---|---|---|
| IC50 | 6 | 6.09 | 7.66 |
| Inhibition | 1 | - | - |
Compounds Tested
| Compound | Name | Phase | Activities | Best pChEMBL |
|---|---|---|---|---|
| CHEMBL34259 | METHOTREXATE | 4.0 | 1 | 7.66 |
| CHEMBL323565 | — | — | 1 | 6.00 |
| CHEMBL225072 | PEMETREXED | 4.0 | 1 | 5.64 |
| CHEMBL223279 | — | — | 1 | 5.05 |
| CHEMBL389051 | — | — | 1 | - |
| CHEMBL374172 | — | — | 2 | - |
Activity Data
| Compound | Name | Type | Rel. | Value | Units | pChEMBL |
|---|---|---|---|---|---|---|
| CHEMBL34259 | METHOTREXATE | IC50 | = | 22.0 | nM | 7.66 |
| CHEMBL323565 | — | IC50 | = | 1000.0 | nM | 6.00 |
| CHEMBL225072 | PEMETREXED | IC50 | = | 2300.0 | nM | 5.64 |
| CHEMBL223279 | — | IC50 | = | 9000.0 | nM | 5.05 |
| CHEMBL389051 | — | IC50 | - | — | - | |
| CHEMBL374172 | — | IC50 | > | 21000.0 | nM | - |
| CHEMBL374172 | — | Inhibition | = | 16.0 | % | - |