Pentoxifylline

CAS No. 6493-05-6

Pentoxifylline( NSC 637086 | Oxpentifylline )

Catalog No. M15464 CAS No. 6493-05-6

A METHYLXANTHINE derivative that inhibits phosphodiesterase and affects blood rheology.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
500MG 38 In Stock
1G 45 In Stock

Biological Information

  • Product Name
    Pentoxifylline
  • Note
    Research use only, not for human use.
  • Brief Description
    A METHYLXANTHINE derivative that inhibits phosphodiesterase and affects blood rheology.
  • Description
    A METHYLXANTHINE derivative that inhibits phosphodiesterase and affects blood rheology. It improves blood flow by increasing erythrocyte and leukocyte flexibility. It also inhibits platelet aggregation. Pentoxifylline modulates immunologic activity by stimulating cytokine production. (In Vitro):Pentoxifylline (0.1-50 mM; 24-48 hours) inhibits cell proliferation in a dose-dependent manner.Pentoxifylline (0.5 mM; 12-36 hours) increases apoptosis and decreases autophagy levels in MDA-MB-231 cells.Pentoxifylline (0.5 mM; 12-36 hours) induces autophagy in MDA-MB-231 cells.Pentoxifylline (0.5 mM; 24-48 hours) blocks cell cycle at the G0/G1 phase.Pentoxifylline results in high LC3-II/LC3-ratio.(In Vivo):Pentoxifylline (200 mg/kg; i.p.) has a protective effect on rats with transient global ischemia and reduces cognitive impairment.
  • In Vitro
    Pentoxifylline (0.1-50 mM; 24-48 hours) inhibits cell proliferation in a dose-dependent manner.Pentoxifylline (0.5 mM; 12-36 hours) increases apoptosis and decreases autophagy levels in MDA-MB-231 cells. Pentoxifylline (0.5 mM; 12-36 hours) induces autophagy in MDA-MB-231 cells.Pentoxifylline (0.5 mM; 24-48 hours) blocks cell cycle at the G0/G1 phase.Pentoxifylline results in high LC3-II/LC3-ratio. Cell Proliferation Assay Cell Line:MDA-MB-231 cells Concentration:0.1 mM, 1 mM, 5 mM , 10 mM, 50 mM Incubation Time:24 hours, 48 hoursResult:Inhibited cell proliferation in a dose-dependent manner.Apoptosis Analysis Cell Line:MDA-MB-231 cells Concentration:0.5 mM Incubation Time:12 hours, 24 hours, 36 hours Result:Induced apoptosis.Cell Autophagy AssayCell Line:MDA-MB-231 cellsConcentration:0.5 mM Incubation Time:24 hours, 48 hours Result:Induced approximately 20-28% of cell autophagy.Cell Cycle Analysis Cell Line:MDA-MB-231 cells Concentration:0.5 mM Incubation Time:24 hours, 48 hours Result:Induced G0/G1 phase arrest.Western Blot Analysis Cell Line:MDA-MB-231 cells Concentration:0.5 mM Incubation Time:24 hours, 48 hours Result:Induced high LC3-II/LC3-ratio.
  • In Vivo
    Pentoxifylline (200 mg/kg; i.p.) has a protective effect on rats with transient global ischemia and reduces cognitive impairment. Animal Model:Adult male Wistar rats 12-13-weeks-old (250-300 g)Dosage:200 mg/kg Administration:Intraperitoneal injection, at 1hr before and 3 hr after ischemia Result:Significantly improved the spatial memory and effects were significant different from those of sham-operated and vehicle groups.
  • Synonyms
    NSC 637086 | Oxpentifylline
  • Pathway
    Apoptosis
  • Target
    Adenosine Receptor
  • Recptor
    A2| PDE
  • Research Area
    Cardiovascular Disease
  • Indication
    ——

Chemical Information

  • CAS Number
    6493-05-6
  • Formula Weight
    278.31
  • Molecular Formula
    C13H18N4O3
  • Purity
    >98% (HPLC)
  • Solubility
    soluble in Water
  • SMILES
    c12c(n(c(=O)n(c1=O)CCCCC(C)=O)C)ncn2C
  • Chemical Name
    1,2,3,6-Tetrahydro-3,7-dimethyl-1-(5-oxohexyl)-2,6-purindion

Shipping & Storage Information

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

Reference

1.Daly JW, et al. Prog Clin Biol Res. 1987;230:41-63.
molnova catalog
related products
  • Theophylline-7-aceti...

    Theophylline-7-acetic acid is a stimulant drug of the xanthine chemical class. It acts as an adenosine receptor antagonist.

  • N6-[2-(4-Aminophenyl...

    A non-selective agonist of Adenosine A3 receptor; has a high affinity for the adenosine A1 and A3 receptors.

  • 8-Cyclopentyl-1,3-di...

    8-Cyclopentyl-1,3-dimethylxanthine?is a potent antagonist of adenosine A1 receptor.