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2'-Deoxy-2',2'-difluorocytidine

CAS No.: 95058-81-4

  • Molecular Formula: Cโ‚‰Hโ‚โ‚Fโ‚‚Nโ‚ƒOโ‚„
  • Molecular Weight: 263.20 g/mol

Chemical type

  • Nucleoside analog
  • Antimetabolite
[1]
  • Cytidine analog
  • Pyrimidine nucleoside derivative
[2]

Key properties

  • Chemotherapeutic agent
  • Interferes with DNA synthesis
[1]
  • High affinity for bacterial transporters (KM 2.5โ€“3.0 ยตM for NupG orthologs; KM 10โ€“13 ยตM for NupC orthologs)
  • 15โ€“100 times higher affinity than human transporter hENT1/SLC29A1
  • Metabolized by gamma-proteobacteria (via cytidine deaminase) to less active deaminated form (2',2'-difluoro-2'-deoxyuridine)
  • Incorporated into DNA/RNA, inhibiting nucleotide metabolism and causing cytotoxicity
  • Competitively inhibited by natural nucleosides like cytidine and uridine
[2]
  • Chemotherapy drug for high-risk liver hepatocellular carcinoma (HCC) patients
  • Shown to have greater sensitivity in treating high-risk HCC patients
[1]
  • Anticancer drug for pancreatic ductal adenocarcinoma and other aggressive cancers
  • Frontline chemotherapy agent
  • Transported and metabolized by tumor-associated bacteria, contributing to chemoresistance
[2]

Classification by use

  • Chemotherapy drugs
[1]
  • Chemotherapy agents
  • Substances involved in bacteria-mediated drug resistance
[2]

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  1. [Cite:1] Anoikis- and m6A-related lncRNA analysis to identify prognostic indicators in liver hepatocellular carcinoma, Electronic Journal of Biotechnology, Volume 79, January 2026, 100701
  2. [Cite:2] Elucidation of the Gemcitabine Transporters of Escherichia coli K-12 and Gamma-Proteobacteria Linked to Gemcitabine-Related Chemoresistance, Int. J. Mol. Sci., 2024, 25(13), 7012