Galanthamine (hydrobromide) (Standard)

CAT:
804-HY-A0009R-01
Size:
5 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Galanthamine (hydrobromide) (Standard) - image 1

Galanthamine (hydrobromide) (Standard)

  • Description:

    Galanthamine (hydrobromide) (Standard) is the analytical standard of Galanthamine (hydrobromide) . This product is intended for research and analytical applications. Galanthamine hydrobromide (Galantamine hydrobromide) is a selective, reversible, competitive, alkaloid AChE inhibitor, with an IC50 of 0.35 µM. Galanthamine hydrobromide is a potent allosteric potentiating ligand (APL) of human α3β4, α4β2, α6β4 nicotinic receptors (nAChRs) . Galanthamine hydrobromide is developed for the research of Alzheimer's disease (AD) [1][2][3].
  • Product Name Alternative:

    Galantamine (hydrobromide) (Standard)
  • UNSPSC:

    12352005
  • Target:

    Cholinesterase (ChE) ; nAChR; Reference Standards
  • Type:

    Reference Standards
  • Related Pathways:

    Membrane Transporter/Ion Channel; Neuronal Signaling; Others
  • Field of Research:

    Neurological Disease
  • Assay Protocol:

    https://www.medchemexpress.com/galanthamine-hydrobromide-standard.html
  • Solubility:

    10 mM in DMSO
  • Smiles:

    O[C@@H]1C[C@@H]2OC3=C4C(CN(C)CC[C@]42C=C1)=CC=C3OC.Br
  • Molecular Formula:

    C17H22BrNO3
  • Molecular Weight:

    368.27
  • References & Citations:

    [1]L J Scott, et al. Galantamine: a review of its use in Alzheimer's disease. Drugs. 2000 Nov;60 (5) :1095-122.|[2]Marek Samochocki, et al. Galantamine is an allosterically potentiating ligand of neuronal nicotinic but not of muscarinic acetylcholine receptors. Pharmacol Exp Ther. 2003 Jun;305 (3) :1024-36.|[3]Acharya Balkrishna, et al. Anti-Acetylcholinesterase Activities of Mono-Herbal Extracts and Exhibited Synergistic Effects of the Phytoconstituents: A Biochemical and Computational Study. Molecules. 2019 Nov; 24 (22) : 4175.|[4]Balpreet Matharu, et al. Galantamine inhibits beta-amyloid aggregation and cytotoxicity. J Neurol Sci. 2009 May 15;280 (1-2) :49-58.|[5]Debby Van Dam, et al. Symptomatic effect of donepezil, rivastigmine, galantamine and memantine on cognitive deficits in the APP23 model. Psychopharmacology (Berl) . 2005 Jun;180 (1) :177-90.|[6]Johan Monbaliu, et al. Pharmacokinetics of galantamine, a cholinesterase inhibitor, in several animal species. Arzneimittelforschung. 2003;53 (7) :486-95.
  • Shipping Conditions:

    Room temperature
  • Scientific Category:

    Reference Standards
  • Clinical Information:

    Launched
  • CAS Number:

    [1953-04-4]