Date published: 2025-9-15

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HEI10 Inhibitors

The class of HEI10 inhibitors comprises a diverse range of compounds that modulate the expression and function of HEI10, a protein involved in recombination and DNA repair processes. Camptothecin, a topoisomerase I inhibitor, directly affects HEI10 by stabilizing the topoisomerase I-DNA complex, leading to DNA breaks during replication. This disruption in DNA repair pathways influences HEI10 by altering the substrate availability for its action on recombination and repair processes. Proteasome inhibitors like MG-132 indirectly affect HEI10 by disrupting proteasome function, altering the degradation of ubiquitinated proteins. This modulation impacts HEI10 expression and function by regulating its protein turnover, thereby influencing cellular processes related to recombination and repair mechanisms. Olaparib, a PARP inhibitor, indirectly influences HEI10 by disrupting PARP-mediated DNA repair pathways, altering the availability of DNA substrates for its recombination function.

Bleomycin induces DNA breaks, indirectly modulating HEI10 by generating free radicals that cause DNA damage and alter the substrate availability for its action on recombination processes. Etoposide, a topoisomerase II inhibitor, directly affects HEI10 by stabilizing the topoisomerase II-DNA complex, leading to DNA breaks during replication. Cisplatin modulates HEI10 indirectly through DNA damage response, activating signaling pathways that affect HEI10 expression and function. Compounds like ATR Inhibitor and Caffeine indirectly impact HEI10 by disrupting ATR and ATM kinase-mediated DNA damage responses, respectively. These alterations in downstream pathways influence HEI10 by altering the availability of substrates for its recombination function. Additionally, 5-Fluorouracil modulates HEI10 indirectly through DNA synthesis inhibition, disrupting DNA replication and affecting the availability of substrates for its recombination function. This class of HEI10 inhibitors provides valuable insights into the intricate mechanisms governing HEI10 expression and function, shedding light on potential avenues for further research in recombination and DNA repair processes.

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