| Weight | 262.193 g/mol | 
|---|---|
| Formula | C9H11FN2O6 | 
| Hydrogen Acceptors | 7 | 
| Hydrogen Donors | 4 | 
| Aromatic Rings | 1 | 
| Rotatable Bonds | 2 | 
5-Fluorouridine (316-46-1)
5-fluorouridine, 18F-labeled
 Score:
          #1644 in Biochemistry
          ,
          #4684 in Chemistry
          
        
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      - Sigma-Aldrich -  5-Fluorouridine84.00 - 466.00 USD
 - Fisher Scientific - Search for 5-Fluorouridine
 - TCI - Search for 5-Fluorouridine
 - Cytokines induce thymidine phosphorylase expression in tumor cells and make them more susceptible to 5-deoxy-5-fluorouridine (Cancer Chemotherapy and Pharmacology, 1993)
 - Sensitivity of Human, Murine, and Rat Cells to 5-Fluorouracil and 5-Deoxy-5-fluorouridine in Relation to Drug-metabolizing Enzymes (Cancer Research, 1986)
 - Inhibition of Ribosomal Ribonucleic Acid Maturation in Novikoff Hepatoma Cells by 5-Fluorouracil and 5-Fluorouridine (Journal of Biological Chemistry, 1973)
 - Induction of thymidine phosphorylase expression and enhancement of efficacy of capecitabine or 5'-deoxy-5-fluorouridine by cyclophosphamide in mammary tumor models. (International Journal of Cancer, 1999)
 - Mechanism of Induction of Gastrointestinal Toxicity in the Mouse by 5-Fluorouracil, 5-Fluorouridine, and 5-Fluoro-2-deoxyuridine (Cancer Research, 1979)
 - Activation of 5'-deoxy-5-fluorouridine by thymidine phosphorylase in human tumors (Chemical & Pharmaceutical Bulletin, 1983)
 - 
            
            Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 5-fluorouridine, 18F-labeled
 - 
          SMILESC1=C(C(=O)NC(=O)N1C2C(C(C(O2)CO)O)O)F
 - 
          InChIKeyFHIDNBAQOFJWCA-UHFFFAOYSA-N
 
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 5-Fluorouridine 
                  