Substance

ID:534

Names and Identifiers
IUPAC name
7-(2,3-dihydroxypropyl)-1,3-dimethyl-2,3,6,7-tetrahydro-1H-purine-2,6-dione
Synonyms
DyphyllineDiprofillineDiprophyllineDTDipropyllineDiprophyllinDiprofillinDihydroxypropyl TheophyllineDihydroxypropyl Theopylin
IUPAC Traditional name
dyphylline
Brand Name
PurifilinTefilanHidroxiteofillinaNeophyllinNeophyllineNeotilinaPropyphyllinProtheophyllineSoluphyllinThealCor-TheophyllineCoronarinNeutrafillinaNeutraphyllinNeutraphyllineSilbephyllinSilbephyllineSolufyllinDyflexGlyfyllinGlyphyllineIphyllinNeo-VasophyllineNeutrafilSolufilinAstrophyllinHiphyllinHyphyllineLiacteminNeophylNeostenovasanNeutroxantinaAfi-PhyllinCoronalGlyphyllinCorphyllinDroxineNeufilSynthophyllineTeofenThefylanAristophyllinAsthmolysinCircain
Registration numbers
CAS Number
PubChem CID
PubChem SID
Properties
Physical Property
Hydrophobicity(logP)
-1.9
Solubility
0.33 g/ml
Molecule Details
Drug Groups
approved
Description
A theophylline derivative with broncho- and vasodilator properties. It is used in the treatment of asthma, cardiac dyspnea, and bronchitis. [PubChem]
Indication
For relief of acute bronchial asthma and for reversible bronchospasm associated with chronic bronchitis and emphysema.
Pharmacology
Dyphylline, a xanthine derivative, is a bronchodilator used for relief of acute bronchial asthma and for reversible bronchospasm associated with chronic bronchitis and emphysema. Dyphylline is a xanthine derivative with pharmacologic actions similar to theophylline and other members of this class of drugs. Its primary action is that of bronchodilation, but it also exhibits peripheral vasodilatory and other smooth muscle relaxant activity to a lesser degree.
Toxicity
LD50=1954 mg/kg (orally in mice)
Affected Organisms
Humans and other mammals
Biotransformation
Hepatic
Half Life
2 hours (range 1.8 - 2.1 hours)
Protein Binding
84%
Elimination
Dyphylline exerts its bronchodilatory effects directly and, unlike the-ophylline, is excreted unchanged by the kidneys without being metabolized by the liver. Approximately 88% of a single oral dose can be recovered from the urine unchanged.
External Links
Molecular Spectra
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References
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