Palmitelaidic Acid

CAS No. 10030-73-6

Palmitelaidic Acid( 9-trans-Hexadecenoic acid | trans-Palmitoleic acid )

Catalog No. M27101 CAS No. 10030-73-6

Palmitelaidic Acid is one of the most abundant fatty acids in serum and tissue.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 54 In Stock
10MG 76 In Stock
25MG 122 In Stock
50MG 176 In Stock
100MG 259 In Stock
200MG 384 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Palmitelaidic Acid
  • Note
    Research use only, not for human use.
  • Brief Description
    Palmitelaidic Acid is one of the most abundant fatty acids in serum and tissue.
  • Description
    Palmitelaidic Acid is one of the most abundant fatty acids in serum and tissue.(In Vitro):Palmitelaidic Acid, described as lipokine, increases glucose uptake by modulation of 5'AMP-activated protein kinase (AMPK), as well as increasing lipolysis by activation of peroxisome proliferator-activated receptor-α (PPARα), in adipose tissue.(In Vivo):C57BL6 and PPARα knockout (KO) mice were fed for 12 weeks with a standard diet (SD) or high-fat diet (HF), and in the last 2 weeks were treated with oleic or Palmitelaidic Acid. Palmitelaidic Acid promoted a faster uptake of glucose in the body, associated with higher insulin concentration; however, even when stimulated with insulin, Palmitelaidic Acid did not modulate the insulin pathway (AKT, IRS). Palmitelaidic Acid increased the phosphorylation of AMPK, upregulated glucokinase and downregulated SREBP-1. Regarding AMPK downstream, Palmitelaidic Acid increased the production of FGF-21 and stimulated the expression of PPARα. Palmitelaidic Acid treatment did not increase AMPK phosphorylation, modulate glucokinase or increase FGF-21 in liver of PPARα KO mice.
  • In Vitro
    The monounsaturated fatty acid palmitoleate (palmitoleic acid) is one of the most abundant fatty acids in serum and tissues, particularly adipose tissue and liver. Its endogenous production by stearoyl-CoA desaturase 1 gives rise to its cis isoform, cis-palmitoleate. Palmitoleic acid has been correlated with multiple cardiometabolic risk factors, including high blood pressure, total cholesterol, TGs, apoA-I, apoB, and endothelial dysfunction.
  • In Vivo
    Palmitoleic acid promotes a faster uptake of glucose in the body, associated with higher insulin concentration. Palmitoleic acid increases the phosphorylation of AMPK, up-regulates glucokinase and down-regulates SREBP-1. Regarding AMPK downstream, palmitoleic acid increases the production of FGF-21 and stimulates the expression of PPARα. Palmitoleic acid reduces body weight increase, ameliorates the development of hyperglycemia and hypertriglyceridemia, and improves insulin sensitivity. Furthermore, palmitoleic acid down-regulates mRNA expressions of proinflammatory adipocytokine genes (TNFα and resistin) in white adipose tissue and lipogenic genes (SREBP-1, FAS, and SCD-1) in liver.
  • Synonyms
    9-trans-Hexadecenoic acid | trans-Palmitoleic acid
  • Pathway
    Cytoskeleton/Cell Adhesion Molecules
  • Target
    Glucokinase
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    10030-73-6
  • Formula Weight
    254.414
  • Molecular Formula
    C16H30O2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?Ethanol : 100 mg/mL (393.07 m)
  • SMILES
    CCCCCC\C=C\CCCCCCCC(O)=O
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Jiasheng Zhou, et al. 430 ferrite stainless steel and production process thereof. CN113462967A
molnova catalog
related products
  • Manghaslin

    Manghaslin has considerable α-glucosidase inhibitory activity, illustrating the anti-diabetic potential of phenolic-rich litchi pulp extracts. Manghaslin also shows inhibitory activity against AChE

  • ML266

    ML266, a glucocerebrosidase (GCase) chaperone with an IC50 of 2.5 μM, facilitates the transport of the mutant protein to the lysosome, thereby restoring GCase activity without inhibiting the enzyme's function.

  • 4'7-DIMETHOXY-5-HYDR...

    4'7-DIMETHOXY-5-HYDROXYFLAVONE can inhibit α-glucosidase and α-amylase enzymes and enhance 2-NBDG uptake in L6 cells it has hypolipidemic effect on mouse pre-adipocyte (3T3L1) cell lines.