PIERCE 1, alternatively termed RbEST47 or C9orf116, is a nuclear protein that functions within specific cellular processes, primarily focusing on the cellular response to DNA damage stimulus. It also plays a significant role in the cellular reaction to UV-C radiation and the intricate process of determining left/right symmetry in organisms. Its nuclear localization signifies its involvement in the regulation and response mechanisms of the cell to external and internal cues, especially those related to genomic integrity and cellular stress.
The class of inhibitors associated with PIERCE 1 can be envisioned as compounds that modulate cellular responses, particularly those pertaining to DNA damage and related stress pathways. These inhibitors typically target intricate molecular pathways that are closely aligned with the preservation of DNA integrity, maintenance of genomic stability, and cellular responses to various stressors. By intervening in these pathways, the inhibitors can indirectly modulate the function and activity of PIERCE 1, although they might not directly bind or interact with the protein itself. Given the multifaceted nature of DNA repair and response mechanisms, these inhibitory compounds can vary widely in their modes of action. Some might focus on enzymes responsible for recognizing and rectifying DNA damage, while others might target kinases that signal the presence of DNA lesions and instigate repair processes. Still, others might affect the scaffolding or mediator proteins that facilitate communication between different components of the DNA damage response. In essence, the inhibitors of this class primarily function by perturbing the equilibrium of the DNA damage response network, consequently influencing the roles and responsibilities of proteins like PIERCE 1 within this network.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Olaparib | 763113-22-0 | sc-302017 sc-302017A sc-302017B | 250 mg 500 mg 1 g | $206.00 $299.00 $485.00 | 10 | |
Olaparib inhibits PARP enzymes involved in DDR, leading to the impairment of DNA repair. Its indirect effects might influence PIERCE1. | ||||||
Ceralasertib | 1352226-88-0 | sc-507439 | 10 mg | $573.00 | ||
AZD6738 is another ATR inhibitor, targeting DDR pathways. Its indirect actions could potentially affect PIERCE1's role in DNA damage. | ||||||
Nutlin-3 | 548472-68-0 | sc-45061 sc-45061A sc-45061B | 1 mg 5 mg 25 mg | $56.00 $212.00 $764.00 | 24 | |
Nutlin-3 stabilizes p53 by inhibiting MDM2, thereby influencing the DNA damage response pathway which might impact PIERCE1 indirectly. | ||||||
Niraparib | 1038915-60-4 | sc-507492 | 10 mg | $150.00 | ||
MK-4827 is a PARP inhibitor that impairs DNA repair processes. Its effects on these pathways might indirectly modulate PIERCE1. | ||||||
Rucaparib | 283173-50-2 | sc-507419 | 5 mg | $150.00 | ||
Another PARP inhibitor that hinders DDR, potentially influencing pathways associated with PIERCE1. | ||||||
2-allyl-1-(6-(2-hydroxypropan-2-yl)pyridin-2-yl)-6-(4-(4-methylpiperazin-1-yl)phenylamino)-1,2-dihydropyrazolo[3,4-d]pyrimidin-3-one | 955365-80-7 | sc-483196 | 5 mg | $340.00 | 1 | |
By inhibiting WEE1, this compound affects cell cycle regulation and DDR. Its indirect effects might play a role in PIERCE1 modulation. | ||||||
ATM Kinase Inhibitor | 587871-26-9 | sc-202963 | 2 mg | $108.00 | 28 | |
ATM kinase inhibitor that affects DDR pathways. The disruption of these pathways could indirectly touch upon PIERCE1's functions. | ||||||
MRN-ATM Pathway Inhibitor, Mirin | 299953-00-7 | sc-203144 | 10 mg | $138.00 | 4 | |
Mirin blocks MRE11-associated DDR. Given PIERCE1's involvement in DDR, this inhibitor could indirectly influence its activity. | ||||||
RAD51 Inhibitor B02 | 1290541-46-6 | sc-507533 | 10 mg | $95.00 | ||
RAD51 inhibitor affecting homologous recombination repair. Could influence PIERCE1 functions linked to DNA damage. | ||||||
ATM/ATR Kinase Inhibitor Inhibitor | 905973-89-9 | sc-202964 | 5 mg | $104.00 | 8 | |
Inhibits ATM/ATR kinases, impacting DDR. The modulation of these pathways might indirectly affect PIERCE1's role in DNA damage. | ||||||