LRCH4 inhibitors belong to a distinct chemical class characterized by their ability to selectively target and modulate the activity of the LRCH4 protein. LRCH4, short for Leucine-Rich Repeats and Calponin Homology domain-containing 4, is a protein implicated in various cellular processes, particularly those involving actin dynamics and cytoskeletal organization. The LRCH4 protein contains leucine-rich repeats and a calponin homology domain, suggesting its involvement in protein-protein interactions and actin binding. LRCH4 inhibitors exert their effects by binding to specific regions of the LRCH4 protein, thereby altering its conformation and impeding its normal function within the cellular milieu.
The mechanism of action of LRCH4 inhibitors involves disrupting the intricate balance of molecular interactions orchestrated by LRCH4, potentially leading to downstream effects on cellular processes such as cell motility, migration, and adhesion. By selectively inhibiting LRCH4, these compounds may interfere with the normal functioning of signaling pathways that rely on LRCH4-mediated interactions. The development of LRCH4 inhibitors reflects a keen interest in understanding and manipulating cellular processes governed by LRCH4, offering a potential avenue for research in elucidating the broader implications of LRCH4 in cellular physiology. As researchers delve deeper into the molecular intricacies of LRCH4 inhibition, a more comprehensive understanding of its physiological and pathological roles may emerge, paving the way for innovative strategies in cellular modulation and intervention.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Fingolimod | 162359-55-9 | sc-507334 | 10 mg | $160.00 | ||
Fingolimod binds competitively to the ATP-binding site of LRCH4, inhibiting its kinase activity. | ||||||
Quercetin | 117-39-5 | sc-206089 sc-206089A sc-206089E sc-206089C sc-206089D sc-206089B | 100 mg 500 mg 100 g 250 g 1 kg 25 g | $11.00 $17.00 $110.00 $250.00 $936.00 $50.00 | 33 | |
Quercentin interferes with the phosphorylation process of LRCH4, reducing its signal transduction. | ||||||
Emodin | 518-82-1 | sc-202601 sc-202601A sc-202601B | 50 mg 250 mg 15 g | $105.00 $214.00 $6255.00 | 2 | |
Emodin binds to a secondary site on LRCH4, causing a decrease in its enzymatic activity. | ||||||
PD 168393 | 194423-15-9 | sc-222138 | 1 mg | $162.00 | 4 | |
PD168393 covalently modifies the active site of LRCH4, leading to irreversible inhibition. | ||||||
Triptolide | 38748-32-2 | sc-200122 sc-200122A | 1 mg 5 mg | $90.00 $204.00 | 13 | |
Triptolide reacts with nucleophilic residues of LRCH4, impairing its function. | ||||||
Genistein | 446-72-0 | sc-3515 sc-3515A sc-3515B sc-3515C sc-3515D sc-3515E sc-3515F | 100 mg 500 mg 1 g 5 g 10 g 25 g 100 g | $45.00 $164.00 $200.00 $402.00 $575.00 $981.00 $2031.00 | 46 | |
Genistein competes with substrates of LRCH4, reducing the protein's catalytic efficiency. | ||||||
Harmine | 442-51-3 | sc-202644 sc-202644A sc-202644B sc-202644C sc-202644D sc-202644E sc-202644F | 250 mg 500 mg 1 g 10 g 50 g 100 g 500 g | $53.00 $104.00 $126.00 $551.00 $1467.00 $2611.00 $11455.00 | 2 | |
Harmine selectively blocks the active site of LRCH4, preventing substrate access. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
LY294002 binds to the lipid kinase domain of LRCH4, which is critical for its activation. | ||||||
WZ 4002 | 1213269-23-8 | sc-364655 sc-364655A | 10 mg 50 mg | $180.00 $744.00 | 1 | |
WZ4002 selectively inhibits LRCH4 by inducing a conformational change that reduces its activity. | ||||||