Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Trypanosoma brucei | adenosine transporter, putative | 0.3987 | 0.5 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
MIC (functional) | = 0.03 ug ml-1 | In vitro minimum inhibitory concentration (MIC) against S. aureus Smith A 9537 at 37 degrees C for 18 hr | ChEMBL. | 2329555 |
MIC (functional) | = 0.25 ug ml-1 | In vitro minimum inhibitory concentration (MIC) against E. faecalis A 9808 at 37 degrees C for 18 h. | ChEMBL. | 2329555 |
MIC (functional) | = 0.25 ug ml-1 | In vitro minimum inhibitory concentration (MIC) against Klebsiella pneumoniae A 9664 at 37 degrees C for 18 h. | ChEMBL. | 2329555 |
MIC (functional) | = 0.5 ug ml-1 | In vitro minimum inhibitory concentration (MIC) against Escherichia coli A 15119 at 37 degrees C for 18 h. | ChEMBL. | 2329555 |
MIC (functional) | = 0.5 ug ml-1 | In vitro minimum inhibitory concentration (MIC) against Enterobacter cloacae A 9656 at 37 degrees C for 18 h. | ChEMBL. | 2329555 |
MIC (functional) | = 0.5 ug ml-1 | In vitro minimum inhibitory concentration (MIC) against Escherichia coli A 15119 at 37 degrees C for 18 h. | ChEMBL. | 2329555 |
MIC (functional) | = 1 ug ml-1 | In vitro minimum inhibitory concentration (MIC) against Morganella morganii A 15153 at 37 degrees C for 18 h. | ChEMBL. | 2329555 |
MIC (functional) | = 1 ug ml-1 | In vitro minimum inhibitory concentration (MIC) against P. aeruginosa A 9843 at 37 degree C for 18 h | ChEMBL. | 2329555 |
MIC (functional) | = 2 ug ml-1 | In vitro minimum inhibitory concentration (MIC) against E. faecium A 24885 at 37 degrees C for 18 h. | ChEMBL. | 2329555 |
MIC (functional) | = 2 ug ml-1 | In vitro minimum inhibitory concentration (MIC) against Serratia marcescens A 20019 at 37 degrees C for 18 hr | ChEMBL. | 2329555 |
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.