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|Storage||at -20°C 2 years|
|SMILES code||CCCCCOC(=O)NC1=NC(=O)N(C=C1F)[[email protected]]2[[email protected]@H]([[email protected]@H]([[email protected]](O2)C)O)O|
|Chemical Name||pentyl [1-(3,4-dihydroxy-5-methyltetrahydrofuran-2-yl)-5-fluoro-2-oxo-1H-pyrimidin-4-yl]carbamate|
Capecitabine is a prodrug, that is enzymatically converted to 5-fluorouracil in the tumor, where it inhibits DNA synthesis and slows growth of tumor tissue. The activation of capecitabine follows a pathway with three enzymatic steps and two intermediary metabolites, 5'-deoxy-5-fluorocytidine (5'-DFCR) and 5'-deoxy-5-fluorouridine (5'-DFUR), to form 5-fluorouracil.
|Solubility (25°C)*||In vitro||DMSO||72 mg/mL (200.36 mM)|
|Water||6 mg/mL (16.69 mM)|
|Ethanol||72 mg/mL (200.36 mM)|
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.
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