Drug intelligence / Profile preview

thioguanine + bleomycin + fludarabine

Development stage
Preclinical
Lead developer
National Cancer Institute
Modality
Recombinant Proteins and Enzymes, Small Molecules
Administration
Intravenous
01

Overview

This is a combination chemotherapy regimen consisting of three antineoplastic agents—thioguanine, bleomycin, and fludarabine. Each component has a distinct mechanism of action: - **Thioguanine** is an antimetabolite (6-thiopurine analogue) that incorporates into DNA and RNA as a false purine base after intracellular activation, disrupting nucleic acid synthesis during the S-phase of the cell cycle. It is primarily used in the treatment of acute nonlymphocytic leukemias[1][7]. - **Bleomycin** is an antibiotic with antitumor activity that induces DNA strand breaks through free radical formation. - **Fludarabine** is also an antimetabolite; it inhibits DNA polymerase alpha, ribonucleotide reductase, and DNA primase after conversion to its active triphosphate form inside cells. This results in inhibition of DNA synthesis and cell death[4][10]. This combination would be expected to have synergistic cytotoxic effects on rapidly dividing malignant cells by targeting different aspects of nucleic acid metabolism and integrity.

02

Targets

POLA1 (DNA polymerase alpha)RNR (Ribonucleotide reductase)DNA-directed primase/polymerase protein (PrimPol)DNALIG1 (DNA ligase 1)

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