Date published: 2025-11-1

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Psg29 Inhibitors

Psg29 inhibitors are a chemical class of compounds designed to inhibit the activity of the Psg29 protein, part of the pregnancy-specific glycoprotein (PSG) family. PSG proteins are a group of carcinoembryonic antigen (CEA)-related cell adhesion molecules known to have diverse functions in various biological processes. The Psg29 protein, like other PSGs, is characterized by its immunoglobulin-like domain structure, making it an important factor in cell-cell adhesion, signaling, and modulation of immune responses. Psg29 inhibitors are small molecules or biologics that specifically bind to the Psg29 protein, hindering its ability to interact with its physiological partners. This inhibition can lead to alterations in signal transduction pathways and downstream cellular effects, depending on the role of Psg29 in different cell types or tissues.

The structural diversity of Psg29 inhibitors is typically influenced by their mode of action, binding specificity, and ability to interfere with the protein's biological functions. These inhibitors may possess functional groups that allow them to establish strong hydrophobic or hydrogen-bonding interactions with the binding pockets of Psg29, effectively blocking its activity. The chemical design of Psg29 inhibitors aims to optimize properties such as binding affinity, selectivity, and stability, ensuring the molecule can effectively engage with Psg29 while minimizing off-target interactions. As a class, Psg29 inhibitors vary in size and structure, ranging from small organic molecules to larger peptides or proteins, with each type offering unique advantages in terms of specificity and potency. Overall, the understanding of Psg29 inhibitors is an ongoing area of biochemical research, with a focus on elucidating their mechanisms of action and improving their molecular interactions with the target protein for enhanced inhibition.

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