IRR inhibitors, also known as ionizing radiation response inhibitors, are a class of chemical compounds designed to modulate cellular responses to ionizing radiation (IR). Ionizing radiation, such as X-rays and gamma rays, induces various DNA lesions and damages, triggering intricate cellular signaling pathways. IRR inhibitors specifically target key components within these signaling cascades, aiming to regulate the cellular response to radiation stress.
These inhibitors play a crucial role in understanding the molecular mechanisms underlying the cellular reactions to ionizing radiation, which is essential for advancing both basic scientific knowledge and potential applications in various fields. One prominent example of IRR inhibitors is those targeting the DNA damage response (DDR) pathway. The DDR pathway is an intricate network of signaling events that coordinates cell cycle checkpoints, DNA repair, and apoptosis in response to DNA damage induced by ionizing radiation. IRR inhibitors may interact with proteins involved in DDR, such as ATM (ataxia-telangiectasia mutated) and ATR (ataxia-telangiectasia and Rad3-related), to modulate their activities. By influencing these critical components, IRR inhibitors provide researchers with valuable tools to dissect the molecular intricacies of cellular responses to ionizing radiation. Understanding the underlying biology facilitated by IRR inhibitors contributes to a broader comprehension of DNA repair mechanisms and aids in the identification of potential targets for further investigation and research in the field of radiation biology.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Vandetanib | 443913-73-3 | sc-220364 sc-220364A | 5 mg 50 mg | $167.00 $1353.00 | ||
Vandetanib is a kinase inhibitor of VEGFR, EGFR and the RET-tyrosine kinase. It might indirectly influence the INSRR protein. |