FDUR
Brand names,
FDUR
Analogs
FDUR
Brand Names Mixture
FDUR
Chemical_Formula
C9H11FN2O5
FDUR
RX_link
http://www.rxlist.com/cgi/generic2/floxuridine.htm
FDUR
fda sheet
FDUR
msds (material safety sheet)
FDUR
Synthesis Reference
No information avaliable
FDUR
Molecular Weight
246.193 g/mol
FDUR
Melting Point
150.5 oC
FDUR
H2O Solubility
1.19E+004 mg/L
FDUR
State
Solid
FDUR
LogP
-1.249
FDUR
Dosage Forms
Powder for solution (500mg vial)
FDUR
Indication
For palliative management of gastrointestinal adenocarcinoma metastatic to the liver, when given by continuous regional intra-arterial infusion in carefully selected patients who are considered incurable by surgery or other means.
FDUR
Pharmacology
Floxuridine is a pyrimidine analog that acts as an inhibitor of the S-phase of cell division. This selectively kills rapidly dividing cells. Floxuridine is an anti-metabolite. Anti-metabolites masquerade as pyramidine-like molecules which prevents normal pyrimidines from being incorporated into DNA during the S phase of the cell cycle. Flurouracil (the end-product of catabolism of floxuridine) blacks an enzyme which converts cytosine nucleosides into the deoxy derivative. In addition, DNA synthesis is further inhibited because fluoruracil blocks the incorporation of the thymdine nucleotide into the DNA strand.
FDUR
Absorption
No information avaliable
FDUR
side effects and Toxicity
Oral, rat LD50: 215 mg/kg. Signs of overdose include nausea, vomiting, diarrhea, gastrointestinal ulceration and bleeding, and bone marrow depression (including thrombocytopenia, leukopenia and agranulocytosis).
FDUR
Patient Information
FDUR
Organisms Affected
Humans and other mammals