Memantine-d6 (hydrochloride)-6

CAT:
804-HY-B0365AS-01
Size:
500 µg

For Laboratory Research Only. Not for Clinical or Personal Use.

  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Memantine-d6 (hydrochloride)-6 - image 1

Memantine-d6 (hydrochloride)-6

  • UNSPSC Description:

    Memantine-d6 (hydrochloride) is the deuterium labeled Memantine hydrochloride. Memantine (hydrochloride) (D-145 (hydrochloride)) is a moderate affinity, uncompetitive NMDA receptor antagonist, inhibit CYP2B6 and CYP2D6 with Ki of 0.51 nM and 94.9 μM, respectively[1].
  • Target Antigen:

    Autophagy; Cytochrome P450; iGluR
  • Type:

    Isotope-Labeled Compounds
  • Related Pathways:

    Autophagy;Membrane Transporter/Ion Channel;Metabolic Enzyme/Protease;Neuronal Signaling
  • Field of Research:

    Neurological Disease
  • Purity:

    98.0
  • Solubility:

    10 mM in DMSO
  • Smiles:

    [2H]C([2H])([2H])[C@@](C[C@@](N)(C[C@@H]1C2)C3)(C1)C[C@@]32C([2H])([2H])[2H].Cl
  • Molecular Weight:

    221.80
  • References & Citations:

    [1]Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. |[2]Robinson, D.M. and G.M. Keating, Memantine: a review of its use in Alzheimer's disease. Drugs, 2006. 66(11): p. 1515-34.|[3]Chen, H.S., et al., Open-channel block of N-methyl-D-aspartate (NMDA) responses by memantine: therapeutic advantage against NMDA receptor-mediated neurotoxicity. J Neurosci, 1992. 12(11): p. 4427-36.|[4]Chen, H.S. and S.A. Lipton, Mechanism of memantine block of NMDA-activated channels in rat retinal ganglion cells: uncompetitive antagonism. J Physiol, 1997. 499 ( Pt 1): p. 27-46.
  • Shipping Conditions:

    Blue Ice
  • Storage Conditions:

    -20°C, 3 years (Powder)
  • Clinical Information:

    No Development Reported
  • CAS Number:

    9007-83-4