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
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- 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)
-
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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