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1,2-Dipalmitoyl-sn-glycerol 3-phosphate sodium

CAS No. 169051-60-9

1,2-Dipalmitoyl-sn-glycerol 3-phosphate sodium( —— )

Catalog No. M23760 CAS No. 169051-60-9

1,2-Dipalmitoyl-sn-glycerol 3-phosphate sodium, a phosphatidic acid, is a human endogenous metabolite.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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5MG 42 In Stock
10MG 61 In Stock
25MG 102 In Stock
50MG 150 In Stock
100MG 224 In Stock
500MG 556 In Stock
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Biological Information

  • Product Name
    1,2-Dipalmitoyl-sn-glycerol 3-phosphate sodium
  • Note
    Research use only, not for human use.
  • Brief Description
    1,2-Dipalmitoyl-sn-glycerol 3-phosphate sodium, a phosphatidic acid, is a human endogenous metabolite.
  • Description
    1,2-Dipalmitoyl-sn-glycerol 3-phosphate sodium, a phosphatidic acid, is a human endogenous metabolite.
  • In Vitro
    Phosphatidic acids are biologically active lipids that can stimulate a large range of responses in many different cell types, such as platelet aggregation, smooth muscle contraction, in vivo vasoactive effects, chemotaxis, expression of adhesion molecules, increased tight junction permeability of endothelial cells, induction of stress fibres, modulation of cardiac contractility, and many others.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Proteasome/Ubiquitin
  • Target
    Endogenous Metabolite
  • Recptor
    Endogenous Metabolite
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    169051-60-9
  • Formula Weight
    670.87
  • Molecular Formula
    C35H68NaO8P
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?H2O : < 0.1 mg/mL (insoluble))
  • SMILES
    O=P(OC[C@H](OC(CCCCCCCCCCCCCCC)=O)COC(CCCCCCCCCCCCCCC)=O)(O[Na])O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Niedernberg A, et al. Sphingosine 1-phosphate and dioleoylphosphatidic acid are low affinity agonists for the orphan receptor GPR63. Cell Signal. 2003 Apr;15(4):435-46.
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