| # | Aladdin ID | Assay Type | Description | Organism | Compounds | Reference | BAO Format | Source | |
|---|---|---|---|---|---|---|---|---|---|
| 1. | ALA666972 | B | Percent binding affinity against dopamine D3 receptor | Rattus norvegicus | 1 | single protein format | Scientific Literature | ||
| 2. | ALA666975 | B | Binding affinity was measured at cloned mammalian dopamine D3 receptor expressed in CHO-K1 cells (using [3H]- spiperone); NA means inactive | 1 | cell-based format | Scientific Literature | |||
| 3. | ALA666976 | B | Binding affinity was measured at cloned mammalian dopamine D3 receptor expressed in CHO-K1 cells (using [3H]- spiperone); NT means not tested | 2 | cell-based format | Scientific Literature | |||
| 4. | ALA666977 | B | Percent inhibition against dopamine D3 receptor at a concentration of 1 umol/L | 1 | single protein format | Scientific Literature | |||
| 5. | ALA666978 | F | Antagonistic activity at D3 receptor using in vitro functional assay | 1 | assay format | Scientific Literature | |||
| 6. | ALA671914 | B | Affinity on C6 glioma cells transfected with Dopamine receptor D3 | Rattus norvegicus | 11 | cell-based format | Scientific Literature | ||
| 7. | ALA673250 | B | Tested for in vitro binding affinity against cloned mammalian dopamine autoreceptor, expressed in CHO-K1 cells, using [3H]spiperone as radioligand | 1 | cell-based format | Scientific Literature | |||
| 8. | ALA679085 | F | Antagonist activity by measuring the inhibition of quinpirole stimulated [3H]- thymidine uptake against Dopamine receptor D3; NA means Not Active | 1 | assay format | Scientific Literature | |||
| 9. | ALA678232 | F | Antagonist activity by measuring the inhibition of quinpirole stimulated [3H]- thymidine uptake against Dopamine receptor D3; the compound is active | 2 | assay format | Scientific Literature | |||
| 10. | ALA678233 | F | Maximal stimulation reached was evaluated by using [35S]- GTP-gamma S radioligand | 1 | assay format | Scientific Literature | |||
| 11. | ALA678234 | B | Saturable binding was tested dopamine receptor D3 in rat striatal membrane homogenate | 1 | cell membrane format | Scientific Literature | |||
| 12. | ALA678235 | F | Agonist activity by measuring the [3H]-thymidine uptake against Dopamine receptor D3 from rat | 1 | assay format | Scientific Literature | |||
| 13. | ALA678236 | F | Agonist activity by measuring the [3H]thymidine uptake against Dopamine receptor D3 from rat | 3 | assay format | Scientific Literature | |||
| 14. | ALA678237 | B | Basal binding towards Dopamine receptor D3 was evaluated using [35S]- GTP-gamma S radioligand | 1 | single protein format | Scientific Literature | |||
| 15. | ALA678238 | F | Effective concentration was determined as thymidine uptake in CHO-L6 cells transfected with the rat Dopamine receptor D3 by mitogenesis assay | 2 | cell-based format | Scientific Literature | |||
| 16. | ALA678239 | F | Effective concentration was determined as thymidine uptake in CHO-L6 cells transfected with the rat Dopamine receptor D3 by mitogenesis assay (intrinsic activity) | 2 | cell-based format | Scientific Literature | |||
| 17. | ALA678240 | B | Concentration of compound required to inhibit the binding of radioligand [3H](R)-7-OH-DPAT to Dopamine receptor D3 in rat striatum | 4 | tissue-based format | Scientific Literature | |||
| 18. | ALA678241 | B | Concentration of compound required to inhibit the binding of radioligand [3H](R)-7-OH-DPAT to Dopamine receptor D3 in rat striatum. | 1 | tissue-based format | Scientific Literature | |||
| 19. | ALA678242 | B | Inhibitory concentration against [3H]spiperone binding to Dopamine receptor D3 expressed in CHO-K1 cells | Rattus norvegicus | 8 | cell-based format | Scientific Literature | ||
| 20. | ALA678243 | B | relative affinity against Dopamine receptor D3 in ventral striatum using [3H](+)-7-OH-DPAT as radioligand | 7 | tissue-based format | Scientific Literature |
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