IBMX
From Infogalactic: the planetary knowledge core
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Names | |||
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IUPAC name
1-methyl-3-(2-methylpropyl)-7H-purine-2,6-dione
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Other names
3-Isobutyl-1-methylxanthine
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Identifiers | |||
28822-58-4 | |||
ChEBI | CHEBI:34795 | ||
ChEMBL | ChEMBL275084 | ||
ChemSpider | 3627 | ||
DrugBank | DB07954 | ||
388 | |||
Jmol 3D model | Interactive image | ||
KEGG | C13708 | ||
PubChem | 3758 | ||
UNII | TBT296U68M | ||
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Properties | |||
C10H14N4O2 | |||
Molar mass | 222.3 g/mol | ||
Appearance | White solid | ||
Melting point | 199 to 201 °C (390 to 394 °F; 472 to 474 K) | ||
Solubility | Soluble in ethanol, DMSO, and methanol | ||
Vapor pressure | {{{value}}} | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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verify (what is ?) | |||
Infobox references | |||
IBMX, 3-isobutyl-1-methylxanthine, like other methylated xanthine derivatives, is both a
- competitive nonselective phosphodiesterase inhibitor [1] which raises intracellular cAMP, activates PKA, inhibits TNF-alpha [2][3] and leukotriene [4] synthesis, and reduces inflammation and innate immunity [4] and
- nonselective adenosine receptor antagonist.[5]
As a phosphodiesterase inhibitor, IBMX has IC50 = 2-50 μM [6] and does not inhibit PDE8 or PDE9.[7]
References
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- ↑ Soderling and Beavo Current Opinion in Cell Biol. 2000 12 174
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