Lidocaine-d10 N-Oxide

CAT:
804-HY-B0185S-01
Size:
2.5 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
Lidocaine-d10 N-Oxide - image 1

Lidocaine-d10 N-Oxide

  • UNSPSC Description:

    N-Oxide Lidocaine-d10 is the deuterium labeled Lidocaine. Lidocaine (Lignocaine) inhibits sodium channels involving complex voltage and using dependence[1]. Lidocaine decreases growth, migration and invasion of gastric carcinoma cells via up-regulating miR-145 expression and further inactivation of MEK/ERK and NF-κB signaling pathways. Lidocaine is an amide derivative and has potential for the research of ventricular arrhythmia[2].
  • Target Antigen:

    Apoptosis; ERK; Isotope-Labeled Compounds; MEK; NF-κB; Sodium Channel
  • Type:

    Isotope-Labeled Compounds
  • Related Pathways:

    Apoptosis;MAPK/ERK Pathway;Membrane Transporter/Ion Channel;NF-κB;Others;Stem Cell/Wnt
  • Field of Research:

    Cancer; Cardiovascular Disease
  • Solubility:

    10 mM in DMSO
  • Smiles:

    N(C(CN(C(C([2H])([2H])[2H])([2H])[2H])(C(C([2H])([2H])[2H])([2H])[2H])=O)=O)C1=C(C)C=CC=C1C
  • Molecular Weight:

    260.40
  • References & Citations:

    [1]Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. |[2]Li Z, et al. Evaluation of the antinociceptive effects of lidocaine and bupivacaine on the tail nerves of healthy rats. Basic Clin Pharmacol Toxicol. 2013 Jul;113(1):31-6.|[3]Cummins TR, et al. Setting up for the block: the mechanism underlying lidocaine's use-dependent inhibition of sodium channels. J Physiol. 2007 Jul 1;582(Pt 1):11.|[4]Sui H, et al. Lidocaine inhibits growth, migration and invasion of gastric carcinoma cells by up-regulation of miR-145. BMC Cancer. 2019 Mar 15;19(1):233.
  • Shipping Conditions:

    Room temperature
  • Clinical Information:

    No Development Reported
  • CAS Number:

    851528-10-4