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5-fluoro-5'-O-nitro-2'-deoxyuridine

structure given in first source

Also Known As:

FDUMN; Uridine, 2'-deoxy-5-fluoro-, 5'-nitrate

Networked: 1 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Heterocyclic Compounds: 198
- 1-Ring Heterocyclic Compounds
  - Pyrimidines: 510
    - Pyrimidine Nucleosides: 50
      - Uridine: 1186
        Deoxyuridine: 331
        Floxuridine: 690
        5-fluoro-5'-O-nitro-2'-deoxyuridine: 1
Nucleic Acids, Nucleotides, and Nucleosides: 1
- Nucleosides: 6847
  - Pyrimidine Nucleosides: 50
    - Uridine: 1186
      - Deoxyuridine: 331
        Floxuridine: 690
        5-fluoro-5'-O-nitro-2'-deoxyuridine: 1
  - Deoxyribonucleosides: 34
    - Deoxyuridine: 331
      - Floxuridine: 690
        5-fluoro-5'-O-nitro-2'-deoxyuridine: 1

Related Diseases

1.	Ascites 11/01/1982 - "FdUMN did not inhibit the activity of purified thymidylate synthetase from Lactobacillus casei and was a poor inhibitor of thymidylate synthetase activity in homogenates of L1210 ascites cells. "

Related Drugs and Biologics

1.	Thymidylate Synthase