Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | neutral amino acid transporter A | 0.3316 | 0.5 | 0.5 |
Schistosoma mansoni | solute carrier family 1 (glial high affinity glutamate transporter | 0.3316 | 0.5 | 0.5 |
Onchocerca volvulus | Excitatory amino acid transporter homolog | 0.3316 | 0.5 | 0.5 |
Echinococcus granulosus | neutral amino acid transporter A | 0.3316 | 0.5 | 0.5 |
Echinococcus multilocularis | neutral amino acid transporter A | 0.3316 | 0.5 | 0.5 |
Mycobacterium tuberculosis | Probable C4-dicarboxylate-transport transmembrane protein DctA | 0.3316 | 0.5 | 0.5 |
Loa Loa (eye worm) | excitatory amino acid transporter | 0.3316 | 0.5 | 0.5 |
Echinococcus granulosus | excitatory amino acid transporter 3 | 0.3316 | 0.5 | 0.5 |
Echinococcus granulosus | neutral amino acid transporter A | 0.3316 | 0.5 | 0.5 |
Echinococcus multilocularis | Excitatory amino acid transporter | 0.3316 | 0.5 | 0.5 |
Echinococcus granulosus | neutral amino acid transporter | 0.3316 | 0.5 | 0.5 |
Echinococcus multilocularis | sodium:dicarboxylate symporter | 0.3316 | 0.5 | 0.5 |
Echinococcus multilocularis | excitatory amino acid transporter 3 | 0.3316 | 0.5 | 0.5 |
Echinococcus multilocularis | neutral amino acid transporter excitatory amino acid transporter | 0.3316 | 0.5 | 0.5 |
Chlamydia trachomatis | glutamate symporter | 0.3316 | 0.5 | 0.5 |
Echinococcus multilocularis | excitatory amino acid transporter 2 | 0.3316 | 0.5 | 0.5 |
Echinococcus granulosus | Excitatory amino acid transporter | 0.3316 | 0.5 | 0.5 |
Echinococcus granulosus | Excitatory amino acid transporter | 0.3316 | 0.5 | 0.5 |
Echinococcus granulosus | sodium:dicarboxylate symporter | 0.3316 | 0.5 | 0.5 |
Echinococcus multilocularis | neutral amino acid transporter A | 0.3316 | 0.5 | 0.5 |
Echinococcus multilocularis | Excitatory amino acid transporter | 0.3316 | 0.5 | 0.5 |
Echinococcus granulosus | excitatory amino acid transporter 2 | 0.3316 | 0.5 | 0.5 |
Wolbachia endosymbiont of Brugia malayi | Na+/H+-dicarboxylate symporter | 0.3316 | 0.5 | 0.5 |
Echinococcus multilocularis | excitatory amino acid transporter 2 | 0.3316 | 0.5 | 0.5 |
Echinococcus granulosus | excitatory amino acid transporter 2 | 0.3316 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Proliferative response (functional) | = 42.7 | Maximal proliferation induced in the presence of the mitogen-PWM ( stimulated blastogenesis)in Mice cells at a dose of 40 ug/mL | ChEMBL. | 2033579 |
Proliferative response (functional) | = 59.9 | Proliferation induced by the mitogen alone-PWM (control blastogenesis), in Mice cells at a dose of 40 ug/mL | ChEMBL. | 2033579 |
Proliferative response (functional) | = 93.7 | Maximal proliferation induced in the presence of the mitogen-Concanavalin A (stimulated blastogenesis)in mice cells dosed at 5 ug/mL | ChEMBL. | 2033579 |
Proliferative response (functional) | = 160.9 | Proliferation induced by the mitogen alone-Concanavalin A (control blastogenesis), in mice cells dosed at 5 ug/mL | ChEMBL. | 2033579 |
Proliferative response (functional) | = 42.7 | Maximal proliferation induced in the presence of the mitogen-PWM ( stimulated blastogenesis)in Mice cells at a dose of 40 ug/mL | ChEMBL. | 2033579 |
Proliferative response (functional) | = 59.9 | Proliferation induced by the mitogen alone-PWM (control blastogenesis), in Mice cells at a dose of 40 ug/mL | ChEMBL. | 2033579 |
Proliferative response (functional) | = 93.7000000000001 | Maximal proliferation induced in the presence of the mitogen-Concanavalin A (stimulated blastogenesis)in mice cells dosed at 5 ug/mL | ChEMBL. | 2033579 |
Proliferative response (functional) | = 160.9 | Proliferation induced by the mitogen alone-Concanavalin A (control blastogenesis), in mice cells dosed at 5 ug/mL | ChEMBL. | 2033579 |
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.
1 literature reference was collected for this gene.