Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Onchocerca volvulus | 0.1074 | 0.3803 | 0.2851 | |
Brugia malayi | Muscle positioning protein 4 | 0.1214 | 0.5022 | 0.1968 |
Onchocerca volvulus | 0.1294 | 0.5712 | 0.5054 | |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.1622 | 0.8561 | 0.8561 |
Onchocerca volvulus | 0.1214 | 0.5022 | 0.4258 | |
Echinococcus granulosus | tissue type plasminogen activator | 0.1787 | 1 | 0.5 |
Toxoplasma gondii | kringle domain-containing protein | 0.1787 | 1 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.1074 | 0.3803 | 0.3532 |
Plasmodium vivax | cysteine repeat modular protein 1, putative | 0.1787 | 1 | 0.5 |
Loa Loa (eye worm) | DOMON domain-containing protein | 0.1074 | 0.3803 | 0.3532 |
Onchocerca volvulus | 0.1074 | 0.3803 | 0.2851 | |
Trypanosoma cruzi | hypothetical protein, conserved | 0.1787 | 1 | 0.5 |
Echinococcus multilocularis | tissue type plasminogen activator | 0.1787 | 1 | 0.5 |
Plasmodium falciparum | cysteine repeat modular protein 1 | 0.1787 | 1 | 0.5 |
Schistosoma mansoni | hypothetical protein | 0.1074 | 0.3803 | 0.3803 |
Onchocerca volvulus | 0.1074 | 0.3803 | 0.2851 | |
Loa Loa (eye worm) | hypothetical protein | 0.1294 | 0.5712 | 0.5525 |
Schistosoma mansoni | hypothetical protein | 0.1787 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.1294 | 0.5712 | 0.5525 |
Loa Loa (eye worm) | TK/ROR protein kinase | 0.1787 | 1 | 1 |
Onchocerca volvulus | 0.1074 | 0.3803 | 0.2851 | |
Leishmania major | hypothetical protein, conserved | 0.1787 | 1 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.1214 | 0.5022 | 0.4806 |
Brugia malayi | Kringle domain containing protein | 0.1787 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.1787 | 1 | 1 |
Onchocerca volvulus | 0.1787 | 1 | 1 | |
Brugia malayi | Trypsin family protein | 0.1294 | 0.5712 | 0.3081 |
Schistosoma mansoni | subfamily S1A unassigned peptidase (S01 family) | 0.1294 | 0.5712 | 0.5712 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (functional) | = 26 uM | Antileishmanial activity against promastigotes form of Leishmania major MRHO/IR/75/ER after 72 hrs by MTT assay | ChEMBL. | 21501907 |
IC50 (functional) | = 111 uM | Antileishmanial activity against promastigotes form of Leishmania major MRHO/IR/75/ER after 48 hrs by MTT assay | ChEMBL. | 21501907 |
IC50 (functional) | = 111 uM | Antileishmanial activity against promastigotes form of Leishmania major MRHO/IR/75/ER after 24 hrs by MTT assay | ChEMBL. | 21501907 |
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.