Rad55 inhibitors are a class of compounds designed to target and inhibit the Rad55 protein, a key component in the homologous recombination (HR) repair pathway. Rad55, along with its partner protein Rad57, plays a crucial role in promoting the formation of Rad51 nucleoprotein filaments, which are essential for repairing DNA double-strand breaks (DSBs) through HR. This process is critical for maintaining genomic stability, as Rad55 stabilizes Rad51 filaments on single-stranded DNA (ssDNA), allowing for the efficient search and pairing with homologous DNA sequences. By inhibiting Rad55, these compounds interfere with the formation and stabilization of Rad51 filaments, thereby disrupting the homologous recombination repair mechanism.
Researchers use Rad55 inhibitors to explore the intricate dynamics of DNA repair pathways and to investigate the specific role of Rad55 in stabilizing the Rad51 filament during the repair of DSBs. Inhibitors of Rad55 are useful tools in studies focused on understanding the redundancy and interactions between different repair proteins and how cells balance homologous recombination with other DNA repair pathways like non-homologous end joining (NHEJ). Through such inhibition, scientists can evaluate how cells respond to DNA damage when key components of HR are disabled, further elucidating the critical checkpoints and repair mechanisms that ensure genomic stability. Additionally, Rad55 inhibitors provide insights into how cells manage replication stress and repair DNA lesions, helping to identify potential vulnerabilities in cellular responses to genotoxic stress.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Hydroxyurea | 127-07-1 | sc-29061 sc-29061A | 5 g 25 g | $76.00 $255.00 | 18 | |
Inhibits ribonucleotide reductase, leading to reduced deoxyribonucleotide pools, potentially affecting DNA repair processes involving Rad55. | ||||||
Camptothecin | 7689-03-4 | sc-200871 sc-200871A sc-200871B | 50 mg 250 mg 100 mg | $57.00 $182.00 $92.00 | 21 | |
Inhibits topoisomerase I, causing DNA breaks, which may increase the demand for Rad55-mediated repair. | ||||||
Etoposide (VP-16) | 33419-42-0 | sc-3512B sc-3512 sc-3512A | 10 mg 100 mg 500 mg | $32.00 $170.00 $385.00 | 63 | |
A topoisomerase II inhibitor, potentially increasing the frequency of DNA double-strand breaks and impacting Rad55 function. | ||||||
Cisplatin | 15663-27-1 | sc-200896 sc-200896A | 100 mg 500 mg | $76.00 $216.00 | 101 | |
Causes DNA crosslinks and damage, potentially requiring Rad55-mediated homologous recombination for repair. | ||||||
Mitomycin C | 50-07-7 | sc-3514A sc-3514 sc-3514B | 2 mg 5 mg 10 mg | $65.00 $99.00 $140.00 | 85 | |
Induces DNA crosslinks, potentially impacting Rad55 function in homologous recombination repair. | ||||||
Bleomycin | 11056-06-7 | sc-507293 | 5 mg | $270.00 | 5 | |
Causes DNA strand breaks, potentially necessitating Rad55-dependent repair pathways. | ||||||
Methyl methanesulfonate | 66-27-3 | sc-250376 sc-250376A | 5 g 25 g | $55.00 $130.00 | 2 | |
Alkylates DNA, leading to damage that may involve Rad55 in the repair process. | ||||||
Olaparib | 763113-22-0 | sc-302017 sc-302017A sc-302017B | 250 mg 500 mg 1 g | $206.00 $299.00 $485.00 | 10 | |
A PARP inhibitor, used to study cancers with defective homologous recombination, potentially impacting Rad55-related pathways. | ||||||
VE 821 | 1232410-49-9 | sc-475878 | 10 mg | $360.00 | ||
Inhibits the ATR kinase, which is involved in DNA damage response, potentially affecting Rad55 function. | ||||||
ATM Kinase Inhibitor | 587871-26-9 | sc-202963 | 2 mg | $108.00 | 28 | |
Targets ATM kinase, a key player in DNA damage response, potentially influencing Rad55 activity. |