Date published: 2025-9-12

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galectin-3 Inhibitors

Galectin-3 is a multifunctional protein that belongs to the family of β-galactoside-binding lectins, characterized by its carbohydrate recognition domain (CRD). It plays a pivotal role in a wide array of biological activities, including but not limited to cell adhesion, cell growth, apoptosis, immune response, and tissue repair. Galectin-3 is found in various cellular compartments, including the cytoplasm, nucleus, and even the extracellular space, which underscores its multifaceted roles. It has a molecular weight of approximately 31 kDa and exists in different forms such as monomers, dimers, or oligomers depending on the environmental conditions. The protein is known for its ability to bind to galactose-containing ligands, thereby mediating its interactions with a host of other proteins, lipids, and even nucleic acids. Researchers employ a variety of techniques like X-ray crystallography, NMR spectroscopy, and computational modeling to understand the complex 3D structure of Galectin-3's CRD, which is crucial for its binding capabilities.

Galectin-3 inhibitors, which are chemical compounds specifically crafted to hinder the activity or expression of Galectin-3, usually target the CRD of this protein. These inhibitors are a heterogenous class, encompassing an array of chemical structures such as small molecules, naturally occurring compounds like flavonoids and alkaloids, and synthetic analogs. The mechanisms by which these compounds exert their inhibitory effects can be broadly classified into two categories: blocking the carbohydrate-binding site and modulating cellular signaling pathways. In the former, the inhibitors compete with natural ligands for the CRD, thereby neutralizing Galectin-3's function. In the latter, they influence intracellular signaling cascades such as NF-κB, MAPK, and PI3K pathways that regulate the expression of Galectin-3.

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