# | Aladdin ID | Assay Type | Description | Organism | Compounds | Reference | BAO Format | Source | |
---|---|---|---|---|---|---|---|---|---|
1. | ALA750485 | B | Binding affinity for nAChR with [3H]-nicotine in rat alpha4 beta2 membranes | 2 | cell membrane format | Scientific Literature | |||
2. | ALA751868 | B | Blockade of Nicotinic acetylcholine receptor alpha4-beta2 | 1 | single protein format | Scientific Literature | |||
3. | ALA751869 | B | Blockage of Nicotinic acetylcholine receptor alpha4-beta2 noncompetitively in CA1 stratum radiatum interneurons | 1 | single protein format | Scientific Literature | |||
4. | ALA751870 | B | Blockage of Nicotinic acetylcholine receptor alpha4-beta2 noncompetitively in acute hippocampal slices | 1 | tissue-based format | Scientific Literature | |||
5. | ALA751871 | B | Blockage of Nicotinic acetylcholine receptor alpha4-beta2 noncompetitively in cultured hippocampal neurons | 1 | tissue-based format | Scientific Literature | |||
6. | ALA3706132 | B | Radioligand Binding: The binding of [3H]MLA was measured using a modification of the methods of Davies et al., Neuropharmacol. 38: 679 (1999). [3H]MLA (Specific Activity=25-35 Ci/mmol) was obtained from Tocris. The binding of [3H]MLA was determined using a 2 h incubation at 21 C. Incubations were conducted in 48-well micro-titre plates and contained about 200 μg of protein per well in a final incubation volume of 300 uL. The incubation buffer was PBS and the final concentration of [3H]MLA was 5 nM. The binding reaction was terminated by filtration of the protein containing bound ligand onto glass fiber filters (GF/B, Brandel) using a Brandel Tissue Harvester at room temperature. Filters were soaked in de-ionized water containing 0.33% polyethyleneimine to reduce non-specific binding. Each filter was washed with PBS (3x1 mL) at room temperature. Non-specific binding was determined by inclusion of 50 uM non-radioactive MLA in selected wells. | Rattus norvegicus | 79 | single protein format | BindingDB Database |