Date published: 2026-1-22

1-800-457-3801

SCBT Portrait Logo
Seach Input

Flotillin-2 Inhibitors

Flotillin-2 inhibitors belong to a distinct chemical class of compounds designed to target and modulate the activity of Flotillin-2, a protein known for its role in membrane microdomains called lipid rafts. Flotillin-2, together with Flotillin-1, forms complexes that facilitate the organization and trafficking of membrane-associated proteins and lipids. By inhibiting Flotillin-2, these compounds can interfere with lipid raft formation and disrupt cellular processes that rely on Flotillin-2-mediated signaling and protein trafficking. The precise mechanisms of Flotillin-2 inhibition may vary among compounds within this class. Some inhibitors directly bind to Flotillin-2, affecting its protein-protein interactions or cellular localization. Others might interfere with the assembly of Flotillin-2 complexes or disrupt lipid raft formation through indirect mechanisms. The study of Flotillin-2 inhibitors has been valuable in understanding the functional roles of Flotillin-2 in cellular processes, including endocytosis, intracellular signaling, and membrane trafficking. By selectively inhibiting Flotillin-2, researchers gain insights into the underlying molecular events that govern lipid raft organization and dynamics, providing critical information about the regulation of membrane-associated processes. Furthermore, Flotillin-2 inhibitors serve as essential tools in cell biology and molecular research, facilitating investigations into the intricate cellular mechanisms that involve lipid rafts and their significance in various physiological and pathological conditions. As research in this area continues to evolve, the implications and applications of Flotillin-2 inhibitors remain subjects of ongoing investigation. The insights gained from these studies contribute to the broader knowledge of membrane microdomain biology and may pave the way for future discoveries and advancements in cellular biology and related scientific fields.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Z-Leu-Val-Gly-diazomethylketone

119670-30-3sc-296837
sc-296837A
25 mg
100 mg
$440.00
$1550.00
(0)

A cathepsin C inhibitor that contains a chloromethyl ketone warhead, designed to bind covalently to the enzyme's active site.

CA-074

134448-10-5sc-202513
1 mg
$321.00
(0)

Although originally developed as a cathepsin B inhibitor, CA-074 can also inhibit cathepsin C at higher concentrations.