Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Loa Loa (eye worm) | hypothetical protein | 0.0029 | 0.0139 | 0.0266 |
Giardia lamblia | GTP-binding nuclear protein RAN/TC4 | 0.0022 | 0 | 0.5 |
Echinococcus granulosus | guanine nucleotide binding protein Gs subunit | 0.0047 | 0.0447 | 0.0856 |
Trypanosoma brucei | importin beta-1 subunit, putative | 0.0029 | 0.0139 | 1 |
Echinococcus multilocularis | conserved hypothetical protein | 0.0578 | 0.9933 | 1 |
Brugia malayi | Importin beta-1 subunit | 0.0029 | 0.0139 | 0.1253 |
Echinococcus multilocularis | importin subunit beta 1 | 0.0029 | 0.0139 | 0.014 |
Echinococcus granulosus | snurportin 1 | 0.0314 | 0.522 | 1 |
Echinococcus multilocularis | conserved hypothetical protein | 0.0578 | 0.9933 | 1 |
Trypanosoma brucei | importin beta-1 subunit, putative | 0.0029 | 0.0139 | 1 |
Trichomonas vaginalis | Importin beta-1 subunit, putative | 0.0024 | 0.0039 | 1 |
Loa Loa (eye worm) | GTP-binding regulatory protein Gs alpha-S chain | 0.0047 | 0.0447 | 0.0856 |
Plasmodium falciparum | importin beta, putative | 0.0029 | 0.0139 | 1 |
Echinococcus granulosus | importin subunit beta 1 | 0.0029 | 0.0139 | 0.0266 |
Toxoplasma gondii | HEAT repeat-containing protein | 0.0029 | 0.0139 | 1 |
Loa Loa (eye worm) | nucleolar RNA-associated protein alpha | 0.0314 | 0.522 | 1 |
Brugia malayi | GTP-binding regulatory protein Gs alpha-S chain, putative | 0.0047 | 0.0447 | 0.4035 |
Echinococcus multilocularis | snurportin 1 | 0.0314 | 0.522 | 0.5255 |
Plasmodium vivax | importin-beta 2, putative | 0.0029 | 0.0139 | 1 |
Schistosoma mansoni | Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) | 0.0047 | 0.0447 | 0.0447 |
Trichomonas vaginalis | Importin beta-1 subunit, putative | 0.0024 | 0.0039 | 1 |
Echinococcus multilocularis | guanine nucleotide binding protein G(s) subunit | 0.0047 | 0.0447 | 0.045 |
Schistosoma mansoni | hypothetical protein | 0.0314 | 0.522 | 0.522 |
Echinococcus multilocularis | guanine nucleotide binding protein G(s) subunit | 0.0047 | 0.0447 | 0.045 |
Echinococcus granulosus | guanine nucleotide binding protein Gs subunit | 0.0047 | 0.0447 | 0.0856 |
Leishmania major | importin beta-1 subunit, putative | 0.0024 | 0.0039 | 1 |
Brugia malayi | RNA, U transporter 1 | 0.0084 | 0.1107 | 1 |
Trichomonas vaginalis | importin beta-1, putative | 0.0024 | 0.0039 | 1 |
Entamoeba histolytica | hypothetical protein | 0.0024 | 0.0039 | 1 |
Schistosoma mansoni | Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) | 0.0047 | 0.0447 | 0.0447 |
Trypanosoma cruzi | importin beta-1 subunit, putative | 0.0024 | 0.0039 | 1 |
Schistosoma mansoni | importin beta-1 | 0.0029 | 0.0139 | 0.0139 |
Schistosoma mansoni | Guanine nucleotide-binding protein G(s) subunit alpha (Adenylate cyclase-stimulating G alpha protein) | 0.0047 | 0.0447 | 0.0447 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (functional) | = 118 uM | Inhibition of GABA uptake into crude synaptosomes prepared from adult rat brain | ChEMBL. | 10639282 |
IC50 (functional) | = 281 uM | Effect of the compound on glial GABA(1 microM) uptake was measured using astrocytes cultured from cerebral cortices of new born mice. | ChEMBL. | 10639282 |
IC50 (functional) | = 281 uM | Effect of the compound on glial GABA(1 microM) uptake was measured using astrocytes cultured from cerebral cortices of new born mice. | ChEMBL. | 10639282 |
IC50 (functional) | = 681 uM | Effect of the compound on neuronal GABA(1 microM) uptake was measured using neurons cultured from cerebral cortices of 15-day-old mouse embryos. | ChEMBL. | 10639282 |
IC50 (functional) | = 681 uM | Effect of the compound on neuronal GABA(1 microM) uptake was measured using neurons cultured from cerebral cortices of 15-day-old mouse embryos. | ChEMBL. | 10639282 |
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.