Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Trypanosoma brucei | adenosine transporter, putative | 0.3832 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Activity (ADMET) | Phytotoxicity against Oryza sativa (rice) plant at two to four-leaf growth stage at <2 g/ha measured after 13 days under green house conditions | ChEMBL. | No reference | |
Activity (ADMET) | = 30 % | Phytotoxicity against Oryza sativa (rice) plant at two to four-leaf growth stage at 500 g/ha measured after 13 days under green house conditions | ChEMBL. | No reference |
Phytotoxicity (functional) | = 0 % | Tested for post-emergent herbicidal activity expressed as phytotoxicity(%) on maize at application rate 500 g/ha | Starlite. | No reference |
Phytotoxicity (functional) | = 0 % | Tested for post-emergent herbicidal activity expressed as phytotoxicity(%) on rice at application rate 500 g/ha | Starlite. | No reference |
Phytotoxicity (functional) | = 0 % | Tesed for post-emergent herbicidal activity expressed as phytotoxicity(%) on wheat at application rate 500 g/ha | Starlite. | No reference |
Phytotoxicity (functional) | = 0 % | Tested for post-emergent herbicidal activity expressed as phytotoxicity(%) on wild oats(Avena Avena fatua) at application rate 500 g/ha | Starlite. | No reference |
Phytotoxicity (functional) | = 0 % | Tested for post-emergent herbicidal activity expressed as phytotoxicity(%) on johnson grass(Sorghum halepense) at application rate 500 g/ha | Starlite. | No reference |
Phytotoxicity (functional) | = 0 % | Tested for post-emergent herbicidal activity expressed as phytotoxicity(%) on Barnyard grass(Echinochloa crus-galli) at application rate 500 g/ha | Starlite. | No reference |
Phytotoxicity (functional) | = 30 % | Tested for post-emergent herbicidal activity expressed as phytotoxicity(%) on green foxtail(Setaria viridis) at application rate 500 g/ha | Starlite. | No reference |
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.