SLUG inhibitors are part of a specialized class of compounds designed to selectively target the SLUG protein, a transcription factor belonging to the Snail family of zinc finger proteins. SLUG, also known as Snail2, plays a significant role in regulating gene expression patterns involved in various cellular processes, including embryonic development, stem cell maintenance, and epithelial-mesenchymal transition (EMT). As a transcriptional regulator, SLUG controls the expression of genes responsible for cell adhesion molecules and other proteins crucial for cell migration and tissue remodeling. SLUG inhibitors are meticulously designed molecules engineered to interact with SLUG, aiming to disrupt its binding to DNA or modulate its role in transcriptional regulation.
Chemically, SLUG inhibitors are developed to selectively bind to specific regions or functional domains of the SLUG protein, interfering with its ability to bind to DNA sequences involved in gene regulation. The molecular structure of these inhibitors is intricately crafted to fit into the binding sites or active regions of SLUG, aiming to obstruct its function without significantly affecting other cellular processes.
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