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5-Fluorouracil

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Category Human immunodeficiency Virus (HIV)
CAS 51-21-8
Description Fluorouracil (5-Fluoracil, 5-FU) is a DNA/RNA synthesis inhibitor, which interrupts nucleotide synthetic by inhibiting thymidylate synthase (TS).
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Product Information

Synonyms 5-FU; Fluorouracil; Adrucil
IUPAC Name 5-fluoro-1H-pyrimidine-2,4-dione
Molecular Weight 130.08
Molecular Formula C4H3FN2O2
Canonical SMILES C1=C(C(=O)NC(=O)N1)F
InChI InChI=1S/C4H3FN2O2/c5-2-1-6-4(9)7-3(2)8/h1H,(H2,6,7,8,9)
InChIKey GHASVSINZRGABV-UHFFFAOYSA-N
Boiling Point 401.4±48.0 °C at 760 mmHg
Melting Point 282-286°C (dec.)(lit.)
Flash Point 196.5±29.6 °C
Purity >98%
Density 1.53 g/cm3
Solubility Soluble in DMF, DMSO, methanol
Appearance White Crystalline Powder
Storage Store at RT
Complexity 199
Exact Mass 130.017853
Index Of Refraction 1.596
In Vitro 5-Fluorouracil (5-Fu) and NSC 123127 (Dox) show synergistic anticancer efficacy. The IC50 value of 5-Fu/Dox-DNM toward human breast cancer (MDA-MB-231) cells is 0.25 μg/mL, presenting an 11.2-fold and 6.1-fold increase in cytotoxicity compared to Dox-DNM and 5-Fu-DNM, respectively.
In Vivo 5-Fluorouracil (23 mg/kg, 3 times/week) for 14 days, induces accelerated gastrointestinal transit associated with acute intestinal inflammation at day 3 after the start of treatment, which may have led to persistent changes in the ENS observed after days 7 and 14 of treatment contributing to delayed gastrointestinal transit and colonic dysmotility
PSA 65.72000
Target Nucleoside Antimetabolite/Analog; HIV; Apoptosis; Endogenous Metabolite
Vapor Pressure 0.0±1.0 mmHg at 25°C
XLogP3-AA -0.9

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