| # | Aladdin ID | Assay Type | Description | Organism | Compounds | Reference | BAO Format | Source | |
|---|---|---|---|---|---|---|---|---|---|
| 1. | ALA692999 | B | Maximum response (E max) against H1 receptor in rat aorta | 1 | tissue-based format | Scientific Literature | |||
| 2. | ALA693000 | B | Relative potency against H1 receptor in rat aorta | 1 | tissue-based format | Scientific Literature | |||
| 3. | ALA857125 | F | Compound was evaluated for mepyramine antagonism effects in rat aorta (relaxation) at a mepyramine concentration of 100 nM | 1 | tissue-based format | Scientific Literature | |||
| 4. | ALA693636 | B | Effective concentration against histamine H1 receptor in rat aorta | 1 | tissue-based format | Scientific Literature | |||
| 5. | ALA693637 | B | Compound was evaluated for binding activity against [3H]pyrilamine as radioligand for Histamine H1 receptor | 1 | single protein format | Scientific Literature | |||
| 6. | ALA693638 | F | Effective concentration for agonism activity in relaxed rat aortic rings with intact endothelium, submaximally precontracted with 15.8 nM U-46,619; ND id no data | 1 | tissue-based format | Scientific Literature | |||
| 7. | ALA693639 | F | Effective concentration for agonism activity in relaxed rat aortic rings with intact endothelium, submaximally precontracted with 15.8 nM U-46,619; ND is no data | 1 | tissue-based format | Scientific Literature | |||
| 8. | ALA693640 | F | Intrinsic activity of the histamine as reported in relaxed rat aortic rings with intact endothelium, submaximally precontracted with 15.8 nM U-46,619 | 1 | tissue-based format | Scientific Literature | |||
| 9. | ALA693641 | B | Maximum response (E max) against H1 receptor in rat aorta | 3 | tissue-based format | Scientific Literature | |||
| 10. | ALA693642 | B | Maximum response (E max) against Histamine H1 receptor endothelium-Denuded rings of guinea pig Aorta | 1 | single protein format | Scientific Literature | |||
| 11. | ALA693643 | B | Relative potency against Histamine H1 receptor in endothelium-Denuded rings of guinea pig Aorta | 1 | tissue-based format | Scientific Literature | |||
| 12. | ALA693644 | F | The compound was evaluated for intrinsic activity i.e. maximum histamine controls relative to contraction evoked by 10 uM PGF2-alpha in in relaxed rat aortic rings | 1 | tissue-based format | Scientific Literature | |||
| 13. | ALA693645 | F | The compound was evaluated for intrinsic activity i.e. maximum histamine controls relative to contraction evoked by 10 uM PGF2-alpha in relaxed rat aortic rings | 1 | tissue-based format | Scientific Literature | |||
| 14. | ALA693646 | F | The compound was evaluated for intrinsic activity in relaxed rat aortic rings with intact endothelium, submaximally precontracted with 15.8 nM U-46,619 | 5 | tissue-based format | Scientific Literature | |||
| 15. | ALA693647 | F | maximum relaxation evoked by carbachol in relaxed rat aortic rings with intact endothelium, submaximally precontracted with 15.8 nM U-46,619 | 1 | tissue-based format | Scientific Literature | |||
| 16. | ALA692701 | B | Binding affinity against Histamine H1 receptor was measured using radioligand ([3H]pyrilamine) binding assay | 1 | single protein format | Scientific Literature | |||
| 17. | ALA692702 | B | Compound tested for its inhibitory activity against Histamine H1 receptor | 7 | single protein format | Scientific Literature | |||
| 18. | ALA692703 | B | Binding affinity towards histamine H1 receptor from rat brain membranes using [3H]mepyramine as radioligand | 6 | assay format | Scientific Literature | |||
| 19. | ALA692704 | B | Binding affinity towards histamine H1 receptor from rat brain membranes using [3H]mepyramine as radioligand; Not tested | 10 | assay format | Scientific Literature | |||
| 20. | ALA692705 | B | Inhibitory binding of [3H]mepyramine to histamine H1 receptors in rat brain membranes | 4 | cell membrane format | Scientific Literature |
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