Species | Target name | Source | Bibliographic reference |
---|---|---|---|
Homo sapiens | ORAI calcium release-activated calcium modulator 1 | References | |
Homo sapiens | ORAI calcium release-activated calcium modulator 3 | Starlite/ChEMBL | References |
Homo sapiens | ORAI calcium release-activated calcium modulator 2 | Starlite/ChEMBL | References |
Homo sapiens | transient receptor potential cation channel, subfamily V, member 6 | Starlite/ChEMBL | References |
Species | Potential target | Known druggable target | Length | Alignment span | Identity |
---|---|---|---|---|---|
Brugia malayi | TRP channel protein nanchung | transient receptor potential cation channel, subfamily V, member 6 | 725 aa | 595 aa | 27.1 % |
Species | Potential target | Raw | Global | Species |
---|---|---|---|---|
Echinococcus granulosus | short transient receptor potential channel 6 | 0.0003 | 0.0002 | 0.0002 |
Schistosoma mansoni | Protein orai-1 | 0.1323 | 1 | 1 |
Echinococcus granulosus | transient receptor potential cation channel | 0.0003 | 0.0002 | 0.0002 |
Schistosoma mansoni | transient receptor potential channel | 0.0003 | 0.0002 | 0.0002 |
Echinococcus multilocularis | short transient receptor potential channel 6 | 0.0003 | 0.0002 | 0.0002 |
Echinococcus multilocularis | transient receptor potential cation channel | 0.0003 | 0.0002 | 0.0002 |
Echinococcus multilocularis | transient receptor potential cation channel | 0.0003 | 0.0002 | 0.0002 |
Echinococcus multilocularis | calcium release activated calcium channel | 0.1323 | 1 | 1 |
Loa Loa (eye worm) | hypothetical protein | 0.0093 | 0.0685 | 0.0685 |
Loa Loa (eye worm) | hypothetical protein | 0.1323 | 1 | 1 |
Echinococcus granulosus | calcium release activated calcium channel | 0.1323 | 1 | 1 |
Schistosoma mansoni | Protein orai-1 | 0.1323 | 1 | 1 |
Activity type | Activity value | Assay description | Source | Reference |
---|---|---|---|---|
IC50 (binding) | = 2.1 uM | Inhibition of ORAl1/2/3 in HEK293 cells assessed as inhibition of Ca2+ influx after 10 mins by FLIPR assay in presence of thapsigargin | ChEMBL. | 23602525 |
IC50 (binding) | = 3.2 uM | Inhibition of ORAl1/2/3 in HEK293 cells assessed as inhibition of Cd2+ influx after 10 mins by FLIPR assay in presence of thapsigargin | ChEMBL. | 23602525 |
IC50 (binding) | = 13.7 uM | Inhibition of human TRPV6 transfected in HEK293 cells assessed as inhibition of Cd2+ influx after 5 mins by FLIPR assay | ChEMBL. | 23602525 |
IC50 (binding) | = 16.3 uM | Inhibition of human TRPV6 transfected in HEK293 cells assessed as inhibition of Ca2+ influx after 5 mins by FLIPR assay | ChEMBL. | 23602525 |
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.