Date published: 2025-12-24

1-800-457-3801

SCBT Portrait Logo
Seach Input

FAT3 Inhibitors

FAT3 inhibitors constitute a well-defined chemical class characterized by their ability to interact with and modify the activity of the FAT3 protein. The FAT3 protein is a prominent member of the FAT (FAT atypical cadherin) family, which plays a pivotal role in mediating cellular adhesion and signaling processes. The FAT family proteins are recognized for their involvement in orchestrating diverse physiological phenomena, ranging from embryonic development and tissue homeostasis to cellular migration and morphogenesis. The inhibitors that target FAT3 are designed with a precise molecular architecture that enables them to bind selectively to specific binding sites on the FAT3 protein surface. This interaction initiates a conformational change in the protein structure, leading to the modulation of downstream intracellular signaling cascades. By engaging with FAT3 in this manner, these inhibitors can affect cellular behaviors by influencing processes such as cytoskeletal rearrangements, cellular polarity, and intercellular communication. The molecular interplay between FAT3 inhibitors and the FAT3 protein holds considerable significance in advancing our understanding of cellular biology. Through the exploration of how these inhibitors alter FAT3-mediated processes, researchers can gain insights into the intricate mechanisms that underlie fundamental cellular functions. Furthermore, these inhibitors offer valuable tools for probing the complexities of cellular adhesion and signaling pathways in various experimental settings. Their selective interaction with FAT3 enables the investigation of specific roles that FAT3 plays in cellular contexts, shedding light on its contribution to developmental processes, tissue organization, and cellular motility. In summary, FAT3 inhibitors represent a chemically distinct class that acts as potent modulators of FAT3 protein activity. By engaging with FAT3 and inducing conformational changes, these inhibitors have the potential to unravel critical insights into cellular behavior and signaling pathways. Their specific interaction with FAT3 underscores their significance as research tools for unraveling the multifaceted roles of the FAT family proteins in various cellular processes.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Lipase Inhibitor, THL

96829-58-2sc-203108
50 mg
$51.00
7
(1)

Orlistat inhibits pancreatic and gastric lipases, reducing the absorption of dietary fats by forming covalent bonds with the enzymes, thus preventing triglyceride breakdown into absorbable free fatty acids.

Citilistat

282526-98-1sc-358100
sc-358100A
250 mg
1 g
$46.00
$102.00
(0)

Similar to Orlistat, Citilistat inhibits pancreatic lipase, thereby reducing fat absorption. It binds to the active site of lipase and prevents hydrolysis of dietary triglycerides into absorbable fatty acids.