Substance

ID:449709

Names and Identifiers
IUPAC name
3,7-dimethyl-1-(5-oxohexyl)-2,3,6,7-tetrahydro-1H-purine-2,6-dione
Synonyms
VazofirinTorentalAgapurinAzupentatPentofluxPentoxifylline
IUPAC Traditional name
3,7-dimethyl-1-(5-oxohexyl)-2,3,6,7-tetrahydro-1H-purine-2,6-dione
Registration numbers
CAS Number
Properties
Pharmacology Properties
Mechanism of Action
Along with erythrocyte activity, pentoxifylline also decreases blood viscosity by reducing plasma fibrinogen concentrations and increasing fibrinolytic activity
Inhibits erythrocyte phosphodiesterase, resulting in an increase in erythrocyte cAMP activity. Subsequently, the erythrocyte membrane becomes more resistant to deformity
Product Information
Application(s)
It also helps prevent strokes, can be used in managing sickle cell disease and improves blood flow to the brain
It is used to treat intermittent claudication resulting from obstructed arteries in the limbs, and vascular dementia
Pentoxifylline has also been used to treat nausea and headaches in the mountains (altitude sickness).
Pentoxifylline improves blood flow through blood vessels and therefore helps with blood circulation in the arms and legs (e.g. intermittent claudication)
Molecule Details
No Data Available
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Molecular Spectra
No Data Available
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References
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• Conde, L.A., Khim.-Farm. Zh., 1986, 20, 493, (rev, pharmacol)
• Mueller, R. et al., Curr. Med. Res. Opin., 1981, 7, 253, (rev)
• Negwer, M., Organic-Chemical Drugs and their Synonyms, 7th edn., Akademie-Verlag, 1994, 3582, (synonyms)
• Lewis, R.J., Sax's Dangerous Properties of Industrial Materials, 8th edn., Van Nostrand Reinhold, 1992, PBU100
• Hinze, H.J., Arzneim.-Forsch., 1971, 21, 1456, (uv, ir, pmr, ms)
• Mohler, W. et al., Arzneim.-Forsch., 1971, 21, 1159, (synth, props)
• Cadis, E. et al., Rev. Chim. (Bucharest), 1986, 37, 335, (synth)
• Martindale, The Extra Pharmacopoeia, 32nd edn., Pharmaceutical Press, 1999, 925
• Popendiker, K. et al., Arzneim.-Forsch., 1971, 21, 1160; 1171, (pharmacol)