Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Rattus norvegicus | Histamine H3 receptor | Starlite/ChEMBL | References |
Homo sapiens | histamine receptor H3 | Starlite/ChEMBL | References |
Homo sapiens | histamine receptor H4 | Starlite/ChEMBL | References |
Species | Potential target | Known druggable target | Length | Alignment span | Identity |
---|---|---|---|---|---|
Loa Loa (eye worm) | hypothetical protein | Histamine H3 receptor | 445 aa | 384 aa | 22.4 % |
Echinococcus granulosus | biogenic amine 5HT receptor | Histamine H3 receptor | 445 aa | 405 aa | 25.2 % |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus multilocularis | plexin a4 | 0.0065 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0032 | 0.2648 | 0.2648 |
Loa Loa (eye worm) | plexin A | 0.0065 | 1 | 1 |
Loa Loa (eye worm) | sema domain-containing protein | 0.0032 | 0.2648 | 0.2648 |
Schistosoma mansoni | plexin | 0.0051 | 0.6953 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0032 | 0.2648 | 0.2648 |
Loa Loa (eye worm) | sema domain-containing protein | 0.0032 | 0.2648 | 0.2648 |
Loa Loa (eye worm) | hypothetical protein | 0.0032 | 0.2648 | 0.2648 |
Loa Loa (eye worm) | hypothetical protein | 0.0032 | 0.2648 | 0.2648 |
Loa Loa (eye worm) | hypothetical protein | 0.0051 | 0.6953 | 0.6953 |
Loa Loa (eye worm) | hypothetical protein | 0.0032 | 0.2648 | 0.2648 |
Onchocerca volvulus | 0.0051 | 0.6953 | 1 | |
Schistosoma mansoni | hypothetical protein | 0.0032 | 0.2648 | 0.3808 |
Brugia malayi | Plexin repeat family protein | 0.0051 | 0.6953 | 0.5856 |
Schistosoma mansoni | hypothetical protein | 0.0032 | 0.2648 | 0.3808 |
Schistosoma mansoni | semaphorin 5-related | 0.0032 | 0.2648 | 0.3808 |
Echinococcus granulosus | plexin a4 | 0.0065 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0032 | 0.2648 | 0.2648 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
Activity (functional) | Antagonist activity at histamine H2 receptor in guinea pig longitudinally mounted ileum assessed as changes in rate of spontaneous beating at 1 uM by cardiotachograph analysis | ChEMBL. | 22222138 | |
Activity (functional) | Antagonist activity at histamine H1 receptor in guinea pig longitudinally mounted ileum assessed as changes in rate of spontaneous beating up to 10 uM by cardiotachograph analysis | ChEMBL. | 22222138 | |
Ki (binding) | <= 4.5 | Displacement of [3H]histamine from human histamine H4 receptor expressed in GPCR97 transfected human SK-N-MC cells | ChEMBL. | 22222138 |
Ki (binding) | = 7.52 | Displacement of [3H]RAMHA from rat histamine H3 receptor in rat cerebral cortex membranes | ChEMBL. | 22222138 |
Ki (binding) | = 7.78 | Displacement of [3H]RAMHA from human histamine H3 receptor expressed in GPCR97 transfected human SK-N-MC cells | ChEMBL. | 22222138 |
pKb (functional) | = 7.56 | Antagonist activity at human histamine H3 receptor expressed in human SK-N-MC cells assessed as inhibition of (R)-alpha-methylhistamine-induced effect after 6 hrs by beta-galactosidase reporter gene assay | ChEMBL. | 22222138 |
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.