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80288-49-9

80288-49-9 structure
80288-49-9 structure

Name 3-(furan-2-ylmethyl)-1,8-dimethyl-7H-purine-2,6-dione
Synonyms 1H-Purine-2,6-dione, 3-(2-furanylmethyl)-3,7-dihydro-1,8-dimethyl-
3-(2-Furylmethyl)-1,8-dimethyl-3,7-dihydro-1H-purine-2,6-dione
furafylline
3-Furfuryl-1,8-dimethylxanthine
3-(furan-2-ylmethyl)-1,8-dimethyl-3,7-dihydro-1H-purine-2,6-dione
Description Furafylline is a potent and selective inhibitor of human cytochrome P450IA2 with an IC50 of 0.07 μM.
Related Catalog
Target

IC50: 0.07 μM (human cytochrome P450IA2)[1]

In Vivo Furafylline is a potent and selective inhibitor of human cytochrome P450IA2 with an IC50 of 0.07 μM in kinase experiment. Furafylline is a methylxanthine derivative that is introduced as a long-acting replacement for theophylline in the treatment of asthma. Administration of Furafylline is associated with an elevation in plasma levels of caffeine, due to inhibition of caffeine oxidation, a reaction catalysed by one or more hydrocarbon-inducible isoenzymes of P450. Furafylline has either very little or no effect on human monooxygenase activities catalysed by other isoenzymes of P450, including P4501ID1, P4501IC, P450IIIA[1].
References

[1]. Sesardic D, et al. Furafylline is a potent and selective inhibitor of cytochrome P450IA2 in man. Br J Clin Pharmacol. 1990 Jun;29(6):651-63.

Density 1.4±0.1 g/cm3
Boiling Point 543.6±60.0 °C at 760 mmHg
Molecular Formula C12H12N4O3
Molecular Weight 260.249
Flash Point 282.6±32.9 °C
Exact Mass 260.090942
PSA 85.82000
LogP -0.24
Vapour Pressure 0.0±1.5 mmHg at 25°C
Index of Refraction 1.637
Storage condition 2-8℃
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2939590000
HS Code 2939590000
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