Lidocaine-d10 N-Oxide
CAT:
804-HY-B0185S-01
Size:
2.5 mg
For Laboratory Research Only. Not for Clinical or Personal Use.
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- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


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 ChannelType:
Isotope-Labeled CompoundsRelated Pathways:
Apoptosis;MAPK/ERK Pathway;Membrane Transporter/Ion Channel;NF-κB;Others;Stem Cell/WntField of Research:
Cancer; Cardiovascular DiseaseSolubility:
10 mM in DMSOSmiles:
N(C(CN(C(C([2H])([2H])[2H])([2H])[2H])(C(C([2H])([2H])[2H])([2H])[2H])=O)=O)C1=C(C)C=CC=C1CMolecular Weight:
260.40References & 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 temperatureClinical Information:
No Development ReportedCAS Number:
851528-10-4