# | Aladdin ID | Assay Type | Description | Organism | Compounds | Reference | BAO Format | Source | |
---|---|---|---|---|---|---|---|---|---|
1. | ALA643978 | B | Compound was evaluated for the elicited effect on adenylate cyclase activity in homogenates of carp retina at 10 uM | Cyprinus carpio | 1 | ALA1121670 | tissue-based format | Scientific Literature | |
2. | ALA643980 | B | Compound was evaluated for the elicited effect on adenylate cyclase activity in homogenates of carp retina at 100 uM | Cyprinus carpio | 1 | ALA1121670 | tissue-based format | Scientific Literature | |
3. | ALA643672 | B | Dopamine sensitive adenylate cyclase activity (stimulation) in homogenates of rat brain striatal tissue was assessed at 50 uM of compound; ++ = 41-60% incresae of cAMP above basal activity | 2 | ALA1121759 | tissue-based format | Scientific Literature | ||
4. | ALA643673 | B | Dopamine sensitive adenylate cyclase activity (stimulation) in homogenates of rat brain striatal tissue was assessed at 50 uM of compound; +++ = 61-80% incresae of cAMP above basal activity | 2 | ALA1121759 | tissue-based format | Scientific Literature | ||
5. | ALA884268 | B | Inhibition of [3H]apomorphine binding to calf caudate membrane preparation (p4) | 17 | ALA1121759 | assay format | Scientific Literature | ||
6. | ALA654452 | B | Inhibition of [3H]spiroperidol binding to calf caudate membrane preparation (p4) | 17 | ALA1121759 | assay format | Scientific Literature | ||
7. | ALA669681 | B | Binding affinity against Dopamine receptor D1 from rat brain corpus striatum membrane | Rattus norvegicus | 9 | ALA1125019 | assay format | Scientific Literature | |
8. | ALA667485 | B | Binding affinity against Dopamine receptor D2 from rat brain corpus striatum membrane | Rattus norvegicus | 9 | ALA1125019 | assay format | Scientific Literature | |
9. | ALA666358 | B | Binding affinity at rat striatal Dopamine receptor D1 using [3H]- SCH-23390 radioligand | Rattus norvegicus | 11 | ALA1124805 | single protein format | Scientific Literature | |
10. | ALA670280 | B | Compound was evaluated for its ability to inhibit dopamine receptor D1 in rat striatum using [3H]SCH-23390 | 5 | ALA1125726 | tissue-based format | Scientific Literature | ||
11. | ALA669517 | F | Compound was evaluated for its ability to inhibit Striatal Dopamine Receptor in rat brain through radioreceptor assay carried out with agonist ligand. | 5 | ALA1125726 | tissue-based format | Scientific Literature | ||
12. | ALA669035 | B | Equilibrium dissociation constant against recombinant Dopamine receptor D1A expressed in COS7 cells | Homo sapiens | 10 | ALA1129489 | cell-based format | Scientific Literature | |
13. | ALA669037 | B | log(1/Kd) value against recombinant Dopamine receptor D1A expressed in COS7 cell | Homo sapiens | 10 | ALA1129489 | cell-based format | Scientific Literature | |
14. | ALA670417 | F | Low-affinity agonist dissociation constant against striatal Dopamine receptor D1A | Rattus norvegicus | 9 | ALA1129489 | assay format | Scientific Literature | |
15. | ALA670947 | F | Agonistic activity against calf striatal Dopamine receptor using [3H]- ADTN radioligand | Bos taurus | 9 | ALA1124805 | assay format | Scientific Literature | |
16. | ALA671063 | F | Agonist required to inhibit Dopamine receptor D2 photoinactivation by 50% with Iodazidoclebopride using [3H]-Spiperone | Canis lupus familiaris | 5 | ALA1122967 | assay format | Scientific Literature | |
17. | ALA674898 | B | Affinity towards Dopamine receptor D1 | Cercopithecidae | 16 | ALA1131163 | single protein format | Scientific Literature | |
18. | ALA672210 | B | Affinity towards Dopamine receptor D2 | 16 | ALA1131163 | single protein format | Scientific Literature | ||
19. | ALA671405 | B | Evaluated for the affinity against Dopamine receptor D2 in rat striatal membranes | 2 | ALA1124163 | cell membrane format | Scientific Literature | ||
20. | ALA671443 | B | Equilibrium dissociation constant against recombinant Dopamine receptor D2A expressed in COS7 cells | 3 | ALA1129489 | cell-based format | Scientific Literature |