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Pentoxifylline

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Category Human immunodeficiency Virus (HIV)
CAS 6493-05-6
Description Pentoxifylline is a competitive nonselective phosphodiesterase inhibitor which raises intracellular cAMP, activates PKA, inhibits TNF and leukotriene synthesis, and reduces inflammation and innate immunity. It improves red blood cell deformability, reduces blood viscosity and decreases the potential for platelet aggregation and thrombus formation. It also reduces AST and ALT levels and may improve liver histological scores in patients with NALFD/NASH, but did not appear to affect cytokines.
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Product Information

Synonyms Trental; PTX; Oxpentifylline
IUPAC Name 3,7-dimethyl-1-(5-oxohexyl)purine-2,6-dione
Molecular Weight 278.31
Molecular Formula C13H18N4O3
Canonical SMILES CC(=O)CCCCN1C(=O)C2=C(N=CN2C)N(C1=O)C
InChI InChI=1S/C13H18N4O3/c1-9(18)6-4-5-7-17-12(19)10-11(14-8-15(10)2)16(3)13(17)20/h8H,4-7H2,1-3H3
InChIKey BYPFEZZEUUWMEJ-UHFFFAOYSA-N
Boiling Point 531.3±56.0 °C at 760 mmHg
Melting Point 98-100°C
Flash Point 275.1±31.8 °C
Purity >98%
Density 1.3±0.1 g/cm3
Solubility In vitro:
10 mM in DMSO
Appearance White to off-white (Solid)
Application Free Radical Scavengers
Storage Powder:
-20°C: 3 years
4°C: 2 years
In solvent:
-80°C: 6 months
-20°C: 1 month
Complexity 426
Exact Mass 278.13789045
Index Of Refraction 1.621
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.
PSA 78.89000
Target Phosphodiesterase (PDE); Autophagy; HIV
Vapor Pressure 0.0±1.4 mmHg at 25°C
XLogP3-AA 0.3

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