The class of chemicals listed as FIGNL1 Activators includes various compounds that indirectly influence FIGNL1 through their effects on DNA repair mechanisms and related signaling pathways. These compounds are not direct activators of FIGNL1 but may impact its function by modulating the cellular environment and processes related to DNA repair.Poly (ADP-ribose) polymerase (PARP) inhibitors such as Olaparib, Rucaparib, Niraparib, Veliparib, and Talazoparib are known for their role in inhibiting DNA repair, particularly in cells deficient in homologous recombination repair mechanisms. By influencing DNA repair pathways, these inhibitors may indirectly affect the function of FIGNL1, which is involved in DNA repair processes.
Inhibitors targeting key proteins involved in the DNA damage response, such as ATR, ATM, CHK1, CHK2, and DNA-PK, can also indirectly impact FIGNL1. These inhibitors alter the cellular response to DNA damage and the regulation of cell cycle checkpoints, which are important processes in DNA repair where FIGNL1 is involved.Compounds like B02, which stabilize RAD51, can enhance homologous recombination, a pathway in which FIGNL1 plays a significant role. Similarly, inhibitors of BRCA1/2, such as MLN4924, by affecting homologous recombination, could indirectly influence FIGNL1
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