Products for Research Use Only

Veratraldehyde-d3

CAT: 0804-HY-N1096S1-01Size: 5 mgDry Ice: NoHazardous: No
Product image 1
1 / 1
CAT#:0804-HY-N1096S1-01Size:5 mg
Selected
24/48H Stock Items & 2 to 6 Weeks non Stock Items.
Quick Request Actions
Description
Veratraldehyde-d3 is the deuterium labeled Veratraldehyde. Veratraldehyde is an orally active aromatic compound and antibacterial agent. Veratraldehyde can be isolated from essential oils of plants such as peppermint and ginger. Veratraldehyde targets the PilY1 protein. Veratraldehyde has antibacterial activity against Pseudomonas aeruginosa. Veratraldehyde has a repellent effect against mosquitoes and ticks. Veratraldehyde can be used as a flavoring agent[1][2][3][4][5][6][7][8].
CAS Number
143318-06-3
UNSPSC
12352005
Target
Bacterial; Isotope-Labeled Compounds; Parasite
Type
Isotope-Labeled Compounds
Related Pathways
Anti-infection; Others
Field of Research
Infection
Purity
96.0
Solubility
10 mM in DMSO|DMSO : 100mg/mL (ultrasonic)
Smiles
O=CC1=CC=C(OC([2H])([2H])[2H])C(OC)=C1
Molecular Formula
C9H7D3O3
Molecular Weight
169.19
References & Citations
[1]Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53 (2) :211-223.|[2]Wahyuningsih T D, et al. Green synthesis of some novel dioxolane compounds from Indonesian essential oils as potential biogreases[C]//AIP Conference Proceedings. AIP Publishing, 2017, 1823 (1) .|[3]Han D, et al. Bacterial biotransformation of phenylpropanoid compounds for producing flavor and fragrance compounds. Journal of the Korean Society for Applied Biological Chemistry, 2013, 56: 125-133. |[4]Bourbonnais R, et al. Electrochemical analysis of the interactions of laccase mediators with lignin model compounds. Biochim Biophys Acta. 1998 Mar 2;1379 (3) :381-90. |[5]Bisen M, et al. Veratraldehyde Inhibits Motility Phenotypes and Targets Biofilm Formation of Pseudomonas aeruginosa: Insights From Computational and Experimental Studies. Chem Biodivers. 2025 May 30:e00074. |[6]Guillén F, et al. Anisaldehyde and Veratraldehyde Acting as Redox Cycling Agents for H (2) O (2) Production by Pleurotus eryngii. Appl Environ Microbiol. 1994 Aug;60 (8) :2811-7. |[7]Kim S I, et al. Repellency of veratraldehyde (3, 4-dimethoxy benzaldehyde) against mosquito females and tick nymphs. Applied Sciences, 2021, 11 (11) : 4861.|[8]Huh HW, et al. Bioanalytical Method Development and Validation of Veratraldehyde and Its Metabolite Veratric Acid in Rat Plasma: An Application for a Pharmacokinetic Study. Molecules. 2020 Jun 17;25 (12) :2800.
Shipping Conditions
Blue Ice
Storage Conditions
-20°C, 3 years (Powder)
Scientific Category
Isotope-Labeled Compounds
Clinical Information
No Development Reported