# | Aladdin ID | Assay Type | Description | Organism | Compounds | Reference | BAO Format | Source | |
---|---|---|---|---|---|---|---|---|---|
1. | ALA749579 | B | Compound was tested for inhibition of of binding of [3H]-MK 801 to NMDA receptor in rat brain membranes up to 100 uM; IA means inactive | Rattus norvegicus | 1 | ALA1132130 | cell membrane format | Scientific Literature | |
2. | ALA749580 | B | Tested for the ability to displace [3H]CGS-19,755 (10 nM) binding in rat forebrain membranes for NMDA receptor | Rattus norvegicus | 3 | ALA1150536 | cell membrane format | Scientific Literature | |
3. | ALA749581 | B | The binding affinity was measured on NMDA receptor using [3H]- CGS-19755 as radioligand. | Rattus norvegicus | 2 | ALA1127031 | single protein format | Scientific Literature | |
4. | ALA750515 | F | Concentration required to positively modulates NMDA receptor | 1 | ALA1126939 | assay format | Scientific Literature | ||
5. | ALA884513 | B | Compound was evaluated for in vitro inhibition of [3H]-GABA release at NMDA receptor. | 1 | ALA1127805 | single protein format | Scientific Literature | ||
6. | ALA750516 | B | Compound was evaluated for in vitro inhibition of [3H]TCP at NMDA receptor. | 1 | ALA1127805 | single protein format | Scientific Literature | ||
7. | ALA750517 | B | Compound was evaluated for in vitro inhibition of cortical slice at NMDA receptor | 1 | ALA1127805 | single protein format | Scientific Literature | ||
8. | ALA750518 | F | Effective dose required for the action of NMDA receptor activity in maximal electroshock anticonvulsant assay | 1 | ALA1130496 | assay format | Scientific Literature | ||
9. | ALA747060 | B | Compound was evaluated for in vitro inhibition of [3H]L-689,560 at NMDA receptor. | 1 | ALA1127805 | single protein format | Scientific Literature | ||
10. | ALA747061 | B | Compound was evaluated for in vitro inhibition of cGMP cerebellar slice at NMDA receptor. | 1 | ALA1127805 | single protein format | Scientific Literature | ||
11. | ALA747062 | B | Compound was evaluated for in vitro inhibition of cortical slice at NMDA receptor | 1 | ALA1127805 | single protein format | Scientific Literature | ||
12. | ALA747063 | B | Compound was evaluated for in vitro inhibition of cortical slice release at NMDA receptor. | 1 | ALA1127805 | single protein format | Scientific Literature | ||
13. | ALA747064 | B | Compound was evaluated for in vitro inhibition of oocytes at NMDA receptor | 2 | ALA1127805 | cell-based format | Scientific Literature | ||
14. | ALA747065 | B | Compound was evaluated for in vitro inhibition of spinal cord at NMDA receptor. | 1 | ALA1127805 | single protein format | Scientific Literature | ||
15. | ALA747066 | B | Compound was evaluated for its binding affinity towards strychnine - insensitive glycine site of NMDA in presence of [3H]- CPP | 5 | ALA1125973 | single protein format | Scientific Literature | ||
16. | ALA747067 | B | Compound was evaluated for its binding affinity towards strychnine - insensitive glycine site of NMDA in presence of [3H]- CPP; NT means not tested | 4 | ALA1125973 | single protein format | Scientific Literature | ||
17. | ALA747068 | B | Concentration required for 50% Inhibition of responses at cloned NR1A/2A N-methyl-D-aspartate (NMDA) expressed in Xenopus oocytes | 4 | ALA1133639 | cell-based format | Scientific Literature | ||
18. | ALA747070 | F | Concentration required for 50% Inhibition of responses at cloned NR1A/2A NMDA expressed in Xenopus oocytes;Slight potentiation of of agonist-induced responses was observed | 3 | ALA1133639 | cell-based format | Scientific Literature | ||
19. | ALA747071 | B | Concentration required for 50% Inhibition of responses at cloned NR1A/2AB N-methyl-D-aspartate (NMDA) expressed in Xenopus oocytes | 3 | ALA1133639 | cell-based format | Scientific Literature | ||
20. | ALA872726 | B | Concentration required for 50% Inhibition of responses at cloned NR1A/2AB N-methyl-D-aspartate (NMDA) expressed in Xenopus oocytes | 1 | ALA1133639 | cell-based format | Scientific Literature |