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Submit ReviewA 582941 is a selective α7 nAChR partial agonist; exhibits high affinity for both rat and human α7 receptors (Ki values are 10.8 and 16.7 nM respectively). Displays ~15-fold selectivity for α7 over 5-HT3 receptors (Ki = 150 nM for 5-HT3).
M. Wt | 280.37 |
Formula | C17H20N4 |
Storage | Desiccate at RT |
Purity | ≥98% (HPLC) |
CAS Number | 848591-90-2 |
PubChem ID | 44190553 |
InChI Key | GTMRUYCIJSNXGB-GASCZTMLSA-N |
Smiles | [H][C@@]12[C@@](CN(C3=CC=C(C4=CC=CC=C4)N=N3)C2)([H])CN(C)C1 |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Solvent | Max Conc. mg/mL | Max Conc. mM | |
---|---|---|---|
Solubility | |||
DMSO | 28.04 | 100 | |
1eq. HCl | 14.02 | 50 |
The following data is based on the product molecular weight 280.37. Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 3.57 mL | 17.83 mL | 35.67 mL |
5 mM | 0.71 mL | 3.57 mL | 7.13 mL |
10 mM | 0.36 mL | 1.78 mL | 3.57 mL |
50 mM | 0.07 mL | 0.36 mL | 0.71 mL |
References are publications that support the biological activity of the product.
Anderson et al (2008) [3H]A-585539 [(1S,4S)-2,2-dimethyl-5-(6-phenylpyridazin-3-yl)-5-aza-2-azoniabicyclo[2.2.1]heptane], a novel high-affinity α7 neuronal nicotinic receptor agonist: radioligand binding characterization to rat and human brain J.Pharmacol.Exp.Ther. 324 179 PMID: 17959745
If you know of a relevant reference for A 582941, please let us know.
Keywords: A 582941, A 582941 supplier, A582941, selective, alpha7, α7, a7, nicotinics, receptors, partial, agonists, Nicotinic, (a7), Receptors, 4341, Tocris Bioscience
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Recognition memory enables us to make judgements about whether or not we have encountered a particular stimulus before. This poster outlines the cellular mechanisms underlying recognition memory and its links to long-term depression, as well as the use of pharmacological intervention to assess the role of neurotransmitters in recognition memory.