Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Mycobacterium ulcerans | carboxylesterase LipQ | 0.0072 | 0 | 0.5 |
Mycobacterium ulcerans | esterase/lipase | 0.0072 | 0 | 0.5 |
Mycobacterium ulcerans | lipase LipI | 0.0072 | 0 | 0.5 |
Mycobacterium tuberculosis | Probable lipase LipH | 0.0072 | 0 | 0.5 |
Toxoplasma gondii | alpha/beta hydrolase fold domain-containing protein | 0.0072 | 0 | 0.5 |
Treponema pallidum | N-acetylphosphinothricin-tripetide-deacetylase | 0.0072 | 0 | 0.5 |
Trichomonas vaginalis | Esterase, putative | 0.0072 | 0 | 0.5 |
Mycobacterium ulcerans | lipase/esterase LipN | 0.0072 | 0 | 0.5 |
Mycobacterium ulcerans | esterase LipW | 0.0072 | 0 | 0.5 |
Mycobacterium tuberculosis | Probable lipase/esterase LipN | 0.0072 | 0 | 0.5 |
Leishmania major | ecotin, putative | 0.0072 | 0 | 0.5 |
Loa Loa (eye worm) | hypothetical protein | 0.4224 | 1 | 1 |
Trypanosoma cruzi | Isoprenylcysteine alpha-carbonyl methylesterase, putative | 0.0072 | 0 | 0.5 |
Schistosoma mansoni | hormone-sensitive lipase (S09 family) | 0.4224 | 1 | 1 |
Trypanosoma brucei | Isoprenylcysteine alpha-carbonyl methylesterase, putative | 0.0072 | 0 | 0.5 |
Schistosoma mansoni | hormone-sensitive lipase (S09 family) | 0.4224 | 1 | 1 |
Brugia malayi | aryl-acylamidase | 0.0072 | 0 | 0.5 |
Onchocerca volvulus | 0.0072 | 0 | 0.5 | |
Mycobacterium tuberculosis | Probable acetyl-hydrolase/esterase LipR | 0.0072 | 0 | 0.5 |
Mycobacterium tuberculosis | Probable esterase LipO | 0.0072 | 0 | 0.5 |
Mycobacterium ulcerans | lipase LipU | 0.0072 | 0 | 0.5 |
Mycobacterium ulcerans | esterase LipC | 0.0072 | 0 | 0.5 |
Mycobacterium tuberculosis | Probable esterase LipM | 0.0072 | 0 | 0.5 |
Trypanosoma cruzi | Alpha/beta hydrolase domain-containing protein | 0.0072 | 0 | 0.5 |
Mycobacterium ulcerans | hypothetical protein | 0.0072 | 0 | 0.5 |
Mycobacterium ulcerans | lipase LipH | 0.0072 | 0 | 0.5 |
Trichomonas vaginalis | conserved hypothetical protein | 0.0072 | 0 | 0.5 |
Mycobacterium ulcerans | lipase LipU | 0.0072 | 0 | 0.5 |
Mycobacterium ulcerans | acetyl hydrolase MbtJ | 0.0072 | 0 | 0.5 |
Schistosoma mansoni | hormone-sensitive lipase (S09 family) | 0.4224 | 1 | 1 |
Echinococcus multilocularis | hormone sensitive lipase | 0.4224 | 1 | 0.5 |
Mycobacterium tuberculosis | Possible lipase LipU | 0.0072 | 0 | 0.5 |
Toxoplasma gondii | alpha/beta hydrolase fold domain-containing protein | 0.0072 | 0 | 0.5 |
Trypanosoma cruzi | Isoprenylcysteine alpha-carbonyl methylesterase, putative | 0.0072 | 0 | 0.5 |
Mycobacterium leprae | Possible lipase LipU | 0.0072 | 0 | 0.5 |
Trichomonas vaginalis | Esterase, putative | 0.0072 | 0 | 0.5 |
Mycobacterium tuberculosis | Probable esterase LipC | 0.0072 | 0 | 0.5 |
Trichomonas vaginalis | Esterase, putative | 0.0072 | 0 | 0.5 |
Leishmania major | hypothetical protein, conserved | 0.0072 | 0 | 0.5 |
Mycobacterium ulcerans | esterase LipO | 0.0072 | 0 | 0.5 |
Mycobacterium ulcerans | membrane-bound esterase LipM | 0.0072 | 0 | 0.5 |
Mycobacterium tuberculosis | Possible esterase LipW | 0.0072 | 0 | 0.5 |
Mycobacterium tuberculosis | Probable esterase/lipase LipF | 0.0072 | 0 | 0.5 |
Mycobacterium tuberculosis | Putative acetyl hydrolase MbtJ | 0.0072 | 0 | 0.5 |
Mycobacterium tuberculosis | Probable carboxylesterase LipQ | 0.0072 | 0 | 0.5 |
Trypanosoma cruzi | serine peptidase, Clan SC, Family S9D | 0.0072 | 0 | 0.5 |
Mycobacterium tuberculosis | Probable non lipolytic carboxylesterase NlhH | 0.0072 | 0 | 0.5 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Inhibition (functional) | = 0 % | Inhibition of histamine stimulated gastric acid secretion in adult mongrel dogs at dose 5 mg/kg given intravenously | ChEMBL. | 4009611 |
Inhibition (functional) | = 79 % | Gastric antisecretory activity in the pylorus-ligated rat and the reduction in acid output was measured after 4 hr by intraperitoneal (ip) administration of 40 mg/kg dose. | ChEMBL. | 4009611 |
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.