Protriptyline-d3Protriptyline-d3 - High-quality laboratory reagent available from Gentaur. Catalog: 804-HY-B0949AS-01.804-HY-B0949AS-01804-HY-B0949AS-01Business & Industrial > Science & LaboratoryProtriptyline-d3
Gentaur
EUR12027-02-21

Protriptyline-d3

CAT:
804-HY-B0949AS-01
Size:
1 mg

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
Protriptyline-d3 - image 1

Protriptyline-d3

  • Description:

    Protriptyline-d3 is deuterium labeled Protriptyline (HY-B0949) . Protriptyline is a potent tricyclic antidepressant (TCA) . Protriptyline inhibits AChE activity with an IC50 value of 0.06 mM and inhibits Aβ self-assembly. Protriptyline can be used for the study of depression and Alzheimers disease[1][2][3].
  • UNSPSC:

    12352005
  • Target:

    Amyloid-β; Cholinesterase (ChE) ; Isotope-Labeled Compounds
  • Type:

    Isotope-Labeled Compounds
  • Related Pathways:

    Neuronal Signaling; Others
  • Field of Research:

    Neurological Disease
  • Solubility:

    10 mM in DMSO
  • Smiles:

    [2H]C([2H])([2H])NCCCC1C2=C(C=CC=C2)C=CC3=C1C=CC=C3
  • Molecular Formula:

    C19H18D3N
  • Molecular Weight:

    266.40
  • References & Citations:

    [1]Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53 (2) :211-216.|[2]Bansode SB, et, al. Molecular investigations of protriptyline as a multi-target directed ligand in Alzheimer's disease. PLoS One. 2014 Aug 20;9 (8) :e105196.|[3]Chang HT, et, al. The mechanism of protriptyline-induced Ca2+ movement and non-Ca2+-triggered cell death in PC3 human prostate cancer cells. J Recept Signal Transduct Res. 2015;35 (5) :429-34.|[4]Tiwari V, et, al. Protriptyline improves spatial memory and reduces oxidative damage by regulating NFκB-BDNF/CREB signaling axis in streptozotocin-induced rat model of Alzheimer's disease. Brain Res. 2021 Mar 1;1754:147261.
  • Shipping Conditions:

    Room temperature
  • Scientific Category:

    Isotope-Labeled Compounds
  • Clinical Information:

    No Development Reported
  • CAS Number:

    [136765-50-9]