Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Rattus norvegicus | Dihydrofolate reductase | Starlite/ChEMBL | References |
Toxoplasma gondii | bifunctional dihydrofolate reductase-thymidylate synthase | Starlite/ChEMBL | References |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Mycobacterium ulcerans | dihydrofolate reductase DfrA | 0.026 | 0.9883 | 1 |
Plasmodium falciparum | bifunctional dihydrofolate reductase-thymidylate synthase | 0.0262 | 1 | 0.5 |
Trypanosoma cruzi | dihydrofolate reductase-thymidylate synthase | 0.0262 | 1 | 0.5 |
Trypanosoma brucei | dihydrofolate reductase-thymidylate synthase | 0.0262 | 1 | 0.5 |
Brugia malayi | dihydrofolate reductase family protein | 0.026 | 0.9883 | 1 |
Onchocerca volvulus | 0.013 | 0 | 0.5 | |
Toxoplasma gondii | bifunctional dihydrofolate reductase-thymidylate synthase | 0.0262 | 1 | 0.5 |
Schistosoma mansoni | dihydrofolate reductase | 0.026 | 0.9883 | 1 |
Mycobacterium tuberculosis | Dihydrofolate reductase DfrA (DHFR) (tetrahydrofolate dehydrogenase) | 0.026 | 0.9883 | 1 |
Echinococcus multilocularis | dihydrofolate reductase | 0.026 | 0.9883 | 1 |
Loa Loa (eye worm) | dihydrofolate reductase | 0.026 | 0.9883 | 1 |
Brugia malayi | Dihydrofolate reductase | 0.026 | 0.9883 | 1 |
Plasmodium vivax | bifunctional dihydrofolate reductase-thymidylate synthase, putative | 0.0262 | 1 | 0.5 |
Echinococcus granulosus | dihydrofolate reductase | 0.026 | 0.9883 | 1 |
Chlamydia trachomatis | dihydrofolate reductase | 0.026 | 0.9883 | 0.5 |
Mycobacterium leprae | DIHYDROFOLATE REDUCTASE DFRA (DHFR) (TETRAHYDROFOLATE DEHYDROGENASE) | 0.026 | 0.9883 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 28.5 | Selectivity ratio of IC50 for rat liver DHFR to IC50 for Toxoplasma gondii DHFR | ChEMBL. | 17552508 |
IC50 (binding) | = 0.16 mM | Inhibition of Toxoplasma gondii DHFR | ChEMBL. | 17552508 |
IC50 (binding) | = 0.16 mM | Inhibition of Toxoplasma gondii DHFR | ChEMBL. | 17552508 |
IC50 (binding) | = 0.7 mM | Inhibition of Mycobacterium avium DHFR | ChEMBL. | 17552508 |
IC50 (binding) | = 0.7 mM | Inhibition of Mycobacterium avium DHFR | ChEMBL. | 17552508 |
IC50 (binding) | = 4.57 mM | Inhibition of rat liver DHFR | ChEMBL. | 17552508 |
IC50 (binding) | = 4.57 mM | Inhibition of rat liver DHFR | ChEMBL. | 17552508 |
IC50 (binding) | = 37.3 mM | Inhibition of Pneumocystis carinii DHFR | ChEMBL. | 17552508 |
IC50 (binding) | = 37.3 mM | Inhibition of Pneumocystis carinii DHFR | ChEMBL. | 17552508 |
IC50 (binding) | = 1.6 uM | Inhibition of Toxoplasma gondii DHFR using dihydrofolic acid substrate and NADPH cofactor by spectrophotometric assay | ChEMBL. | 20117005 |
IC50 (binding) | = 8.1 uM | Inhibition of rat liver DHFR using dihydrofolic acid substrate and NADPH cofactor by spectrophotometric assay | ChEMBL. | 20117005 |
Ratio IC50 (binding) | = 0.1 | Selectivity ratio of IC50 for rat liver DHFR to IC50 for Pneumocystis carinii DHFR | ChEMBL. | 17552508 |
Ratio IC50 (binding) | = 6.5 | Selectivity ratio of IC50 for rat liver DHFR to IC50 for Mycobacterium avium DHFR | ChEMBL. | 17552508 |
Many chemical entities in TDR Targets come from high-throughput screenings with whole cells or tissue samples, and not all assayed compounds have been tested against a single a single target protein, probably because they get ruled out during screening process. Even if these compounds may have not been of interest in the original screening, they may come as interesting leads for other screening assays. Furthermore, we may be able to propose drug-target associations using chemical similarities and network patterns.
2 literature references were collected for this gene.