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Neuroscience Neurotransmitter Acetylcholine

Galanthamine hydrobromide, Alkaloid acetylcholinesterase inhibitor (ab141114)

Key features and details

  • Alkaloid acetylcholinesterase inhibitor
  • CAS Number: 1953-04-4
  • Purity: > 99%
  • Soluble in water to 50 mM and in DMSO to 100 mM
  • Form / State: Solid

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Overview

  • Product name

    Galanthamine hydrobromide, Alkaloid acetylcholinesterase inhibitor
  • Description

    Alkaloid acetylcholinesterase inhibitor
  • Alternative names

    • Galantamine
  • Biological description

    Alkaloid acetylcholinesterase inhibitor (IC50 values are 0.85 and 12.1 μM for AChE and butyrylcholinesterase, respectively). Blood-brain barrier permeable. Active in vivo following oral administration. Prevents beta-amyloid induced apotosis. Reduces neurodegeneration in vivo.

  • Purity

    > 99%
  • CAS Number

    1953-04-4
  • Chemical structure

    Chemical Structure

Properties

  • Chemical name

    (4aS,6R,8aS)-4a,5,9,10,11,12-Hexahydro-3-methoxy-11-methyl-6H-benzofuro[3a,3,2-ef][2]benzazepin-6-ol hydrobromide
  • Molecular weight

    368.27
  • Molecular formula

    C17H21NO3.HBr
  • PubChem identifier

    121587
  • Storage instructions

    Store at -20°C. Store under desiccating conditions. The product can be stored for up to 12 months.
  • Solubility overview

    Soluble in water to 50 mM and in DMSO to 100 mM
  • Handling

    Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

    Toxic, refer to SDS for further information.

    Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

  • SMILES

    Br.O[C@H]1C=C[C@@]42CCN(C)Cc3ccc(OC)c(O[C@H]2C1)c34
  • Research areas

    • Neuroscience
    • Neurotransmitter
    • Acetylcholine
    • Epigenetics and Nuclear Signaling
    • DNA / RNA
    • DNA Synthesis
    • Topoisomerases
    • Signal Transduction
    • Metabolism
    • Energy Metabolism
    • Cancer
    • Cancer Metabolism
    • Metabolic signaling pathway
    • Metabolism of lipids and lipoproteins
    • Biochemicals
    • Product Range
    • Just Add Water
    • Biochemicals
    • Chemical Type
    • Biochemicals
    • Biochemicals
    • Pharmacology
    • Signaling
    • Amyloidogenesis
    • Biochemicals
    • Pharmacology
    • Enzymes
    • Cholinesterase
    • Inhibitors
    • Metabolism
    • Pathways and Processes
    • Metabolic signaling pathways
    • Lipid and lipoprotein metabolism
    • Lipid metabolism
    • Metabolism
    • Pathways and Processes
    • Metabolic signaling pathways
    • Energy transfer pathways
    • Energy Metabolism
    • Biochemicals
    • Research Area
    • Heart disease
    • Signaling
    • Amyloidogenesis
    • Biochemicals
    • Research Area
    • Pain & inflammation
    • Signaling
    • Amyloidogenesis
    • Biochemicals
    • Research Area
    • Alzheimer's Disease
    • Signaling
    • Amyloidogenesis
    • Biochemicals
    • Research Area
    • Diabetes
    • Signaling
    • Amyloidogenesis
    • Biochemicals
    • Research Area
    • Hypertension
    • Signaling
    • Amyloidogenesis
    • Biochemicals
    • Research Area
    • Obesity
    • Signaling
    • Amyloidogenesis
    • Biochemicals
    • Research Area
    • Respiratory disease
    • Signaling
    • Amyloidogenesis
    • Biochemicals
    • Research Area
    • Stroke
    • Signaling
    • Amyloidogenesis

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Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
For licensing inquiries, please contact partnerships@abcam.com

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