The chemical class referred to as DNA Pol ε A Activators encompasses a range of compounds that, while not directly activating DNA Polymerase epsilon A (DNA Pol ε A), have the potential to influence its activity through the modulation of associated cellular pathways and processes. DNA Pol ε A is crucial in DNA replication and repair, ensuring the fidelity and integrity of genetic information during cell division. The compounds in this class, such as Aphidicolin, Gemcitabine, and 5-Fluorouracil, primarily interact with processes of DNA synthesis and replication. Their role in altering DNA synthesis can create indirect effects on the cellular environment in which DNA Pol ε A operates. For instance, Aphidicolin, by inhibiting DNA synthesis, could potentially create a cellular context that necessitates enhanced activity of DNA replication machinery, including DNA Pol ε A. Similarly, nucleoside analogs like Gemcitabine, which get incorporated into DNA, might indirectly necessitate an increased activity of DNA repair mechanisms, potentially influencing the function of DNA Pol ε A.
Furthermore, this class includes compounds such as Hydroxyurea, Cisplatin, and Etoposide, which affect various aspects of DNA replication and repair. Hydroxyurea, by inhibiting ribonucleotide reductase, impacts deoxyribonucleotide levels and thus could affect the replication process where DNA Pol ε A is involved. Cisplatin and Carboplatin, known for forming DNA adducts, might indirectly impact the DNA repair pathways, potentially influencing the role of DNA Pol ε A in these processes. Similarly, topoisomerase inhibitors like Etoposide and Camptothecin could indirectly affect the replication process, potentially necessitating an enhanced role for DNA Pol ε A. Other agents in this class, such as the anthracycline antibiotic Doxorubicin and the PARP inhibitor Olaparib, demonstrate the potential for altering the DNA repair mechanisms, which could indirectly impact the activity of DNA Pol ε A.
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