BRAT1 inhibitors are a class of compounds that reduce or block the activity of the BRAT1 (BRCA1-associated ATM activator 1) protein, encoded by the BRAT1 gene on chromosome 10. The BRAT1 protein is involved in vital cellular processes, including the DNA damage response, regulation of the cell cycle, and apoptosis. It interacts with other proteins such as ATM (Ataxia-telangiectasia mutated) and BRCA1, which are key players in the DNA repair and genomic stability pathways. The proper functioning of BRAT1 ensures that cells can effectively respond to DNA damage, making it a crucial component of the cellular response to genotoxic stress. The BRAT1 gene is widely expressed across different tissues, with particularly high expression in cells undergoing significant replication or stress, such as neurons.
BRAT1 inhibitors work by reducing the activity of this protein, enabling researchers to dissect its biological roles and contributions to cellular signaling. These inhibitors can vary chemically, ranging from small molecules to more complex entities designed to interfere with BRAT1's interactions with its protein partners. By studying the effects of BRAT1 inhibition, researchers gain insights into the pathways it regulates, such as its involvement in the DNA damage response or its role in maintaining cellular homeostasis. The exploration of structure-activity relationships in BRAT1 inhibitors helps to determine how different chemical modifications can affect their binding affinity and specificity for the BRAT1 protein. These investigations contribute to a broader understanding of BRAT1's function in cellular systems and its regulatory networks.
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