17-DIMETHYLXANTHINE

CAS No. 611-59-6

17-DIMETHYLXANTHINE ( Paraxanthine )

Catalog No. M19728 CAS No. 611-59-6

Paraxanthine is a metabolite of caffeine (sc-202514) which functions as an adenosine receptor ligand and a PARP-1 inhibitor in pulmonary epithelial cells.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
25MG 51 In Stock
50MG 77 In Stock
100MG 109 In Stock
200MG 161 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    17-DIMETHYLXANTHINE
  • Note
    Research use only not for human use.
  • Brief Description
    Paraxanthine is a metabolite of caffeine (sc-202514) which functions as an adenosine receptor ligand and a PARP-1 inhibitor in pulmonary epithelial cells.
  • Description
    Paraxanthine is a metabolite of caffeine (sc-202514) which functions as an adenosine receptor ligand and a PARP-1 inhibitor in pulmonary epithelial cells. Studies suggest that Paraxanthine is structurally similar to caffeine and possibly mediates the physiological effects of caffeine. Also Paraxanthine acts as a competitive phosphodiesterase inhibitor which increases intracellular cAMP activates PKA inhibits TNF-α and leukotriene synthesis. In addition Paraxanthine acts as a Na+/K+ ATPase enzymatic effector.
  • Synonyms
    Paraxanthine
  • Pathway
    Proteasome/Ubiquitin
  • Target
    Endogenous Metabolite
  • Recptor
    Human Endogenous Metabolite
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    611-59-6
  • Formula Weight
    180.16
  • Molecular Formula
    C7H8N4O2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:10 mM;Water:1mg/mL
  • SMILES
    Cn1cnc2[nH]c(=O)n(C)c(=O)c12
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Jiang M Kameda K Han L K et al. Isolation of lipolytic substances caffeine and 17-dimethylxanthine from the stem and rhizome of Sinomenium actum[J]. Planta Medica 1998 64(04):375-377.
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