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 |
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1G | 45 | In Stock |
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Biological Information
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Product NamePentoxifylline
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NoteResearch use only, not for human use.
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Brief DescriptionA METHYLXANTHINE derivative that inhibits phosphodiesterase and affects blood rheology.
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DescriptionA 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.
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In VitroPentoxifylline (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.
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In VivoPentoxifylline (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.
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SynonymsNSC 637086 | Oxpentifylline
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PathwayApoptosis
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TargetAdenosine Receptor
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RecptorA2| PDE
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Research AreaCardiovascular Disease
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Indication——
Chemical Information
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CAS Number6493-05-6
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Formula Weight278.31
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Molecular FormulaC13H18N4O3
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Purity>98% (HPLC)
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Solubilitysoluble in Water
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SMILESc12c(n(c(=O)n(c1=O)CCCCC(C)=O)C)ncn2C
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Chemical Name1,2,3,6-Tetrahydro-3,7-dimethyl-1-(5-oxohexyl)-2,6-purindion
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Daly JW, et al. Prog Clin Biol Res. 1987;230:41-63.
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