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A 582941 HCl (848591-90-2(free base))

Catalog No. T8725

A-582941 is a alpha7 neuronal nicotinic receptor agonist with broad spectrum cognition-enhancing properties

A 582941 HCl (848591-90-2(free base))

A 582941 HCl (848591-90-2(free base))

Purity: 99.83%
Catalog No. T8725
A-582941 is a alpha7 neuronal nicotinic receptor agonist with broad spectrum cognition-enhancing properties
Pack SizePriceAvailabilityQuantity
1 mg$80In Stock
5 mg$181In Stock
10 mg$272In Stock
25 mg$448In Stock
50 mg$630In Stock
100 mg$852In Stock
200 mg$1,130In Stock
1 mL x 10 mM (in DMSO)$178In Stock
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Purity:99.83%
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Product Introduction

Bioactivity
Description
A-582941 is a alpha7 neuronal nicotinic receptor agonist with broad spectrum cognition-enhancing properties
In vitro
A-582941 was found to exhibit high-affinity binding and partial agonism at alpha7 nAChRs, with acceptable pharmacokinetic properties and excellent distribution to the central nervous system (CNS).?In vitro and in vivo studies indicated that A-582941 activates signaling pathways known to be involved in cognitive function such as ERK1/2 and CREB phosphorylation.?A-582941 enhanced cognitive performance in behavioral models that capture domains of working memory, short-term recognition memory, memory consolidation, and sensory gating deficit.?A-582941 exhibited a benign secondary pharmacodynamic and tolerability profile as assessed in a battery of assays of cardiovascular, gastrointestinal, and CNS function[1].
Chemical Properties
Molecular Weight316.83
FormulaC17H21ClN4
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 12 mg/mL (37.88 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.1563 mL15.7813 mL31.5627 mL157.8133 mL
5 mM0.6313 mL3.1563 mL6.3125 mL31.5627 mL
10 mM0.3156 mL1.5781 mL3.1563 mL15.7813 mL
20 mM0.1578 mL0.7891 mL1.5781 mL7.8907 mL

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Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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