LOXL4 inhibitors belong to a distinctive class of chemical compounds designed to target and impede the activity of lysyl oxidase-like 4 (LOXL4), an enzyme that plays a crucial role in the extracellular matrix (ECM) remodeling and maintenance of tissue structure. LOXL4 is a member of the lysyl oxidase (LOX) family of enzymes, which are primarily responsible for catalyzing the cross-linking of collagen and elastin fibers in the ECM. The cross-linking process is essential for providing mechanical strength and stability to connective tissues such as skin, blood vessels, and organs. Inhibition of LOXL4, therefore, is of interest in various contexts, including pathological conditions where aberrant ECM remodeling is implicated, such as fibrosis and certain types of cancers.
LOXL4 inhibitors are designed to interact selectively with the active site of the LOXL4 enzyme, preventing its normal catalytic function. By disrupting the enzymatic activity of LOXL4, these inhibitors have the potential to modulate the deposition and organization of extracellular matrix components, which may have downstream effects on cell behavior, tissue architecture, and overall physiological homeostasis. The development of LOXL4 inhibitors represents a targeted approach to intervene in specific biological pathways associated with ECM remodeling, offering insights into potential strategies for addressing disorders characterized by dysregulated tissue structure and function.
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