Docosanoic acid-d3

CAT:
804-HY-W013049S3-01
Size:
5 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Docosanoic acid-d3 - image 1

Docosanoic acid-d3

  • Description:

    Docosanoic acid-d3 (Behenic acid-d3) is the deuterium labeled Docosanoic acid (HY-W013049) . Docosanoic acid (Behenic acid) is a long-chain saturated fatty acid. Docosanoic acid inhibits the double-stranded DNA (dsDNA) binding activity of p53 DNA binding domain, with a Kd of 12 nM. Docosanoic acid has low bioavailability and can increase cholesterol in humans[1][2][3].
  • Product Name Alternative:

    Behenic acid-d3
  • UNSPSC:

    12352211
  • Hazard Statement:

    H302, H315, H319, H335
  • Target:

    DNA/RNA Synthesis; Endogenous Metabolite; Isotope-Labeled Compounds
  • Type:

    Isotope-Labeled Compounds
  • Related Pathways:

    Cell Cycle/DNA Damage; Metabolic Enzyme/Protease; Others
  • Applications:

    Metabolism-protein/nucleotide metabolism
  • Field of Research:

    Cancer; Metabolic Disease
  • Purity:

    99.79
  • Solubility:

    DMSO : 1 mg/mL (ultrasonic)
  • Smiles:

    [2H]C([2H])([2H])CCCCCCCCCCCCCCCCCCCCC(O)=O
  • Molecular Formula:

    C22H41D3O2
  • Molecular Weight:

    343.60
  • Precautions:

    H302, H315, H319, H335
  • References & Citations:

    [1]Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53 (2) :211-216.|[2]Cater NB, et al. Behenic acid is a cholesterol-raising saturated fatty acid in humans. Am J Clin Nutr. 2001 Jan;73 (1) :41-4.|[3]Moreira DK, et al. Evaluation of structured lipids with behenic acid in the prevention of obesity. Food Res Int. 2017 May;95:52-58. |[4]Iijima H, et al. The inhibitory action of long-chain fatty acids on the DNA binding activity of p53. Lipids. 2006 Jun;41 (6) :521-7.
  • Shipping Conditions:

    Room Temperature
  • Storage Conditions:

    -20°C, 3 years; 4°C, 2 years (Powder)
  • Scientific Category:

    Isotope-Labeled Compounds
  • Clinical Information:

    No Development Reported
  • CAS Number:

    [1193721-67-3]