V-ATPase A4 inhibitors belong to a specific class of chemical compounds that target a crucial cellular mechanism known as Vacuolar-type ATPase (V-ATPase). V-ATPases are multisubunit enzymes found in the membranes of various cellular compartments, including endosomes, lysosomes, and the plasma membrane. They play a pivotal role in maintaining cellular pH homeostasis and regulating the acidity within these compartments. V-ATPase A4 is one of the isoforms of this enzyme, primarily found in certain tissues and cell types. Inhibitors of V-ATPase A4 specifically interfere with the activity of this isoform, disrupting the normal functioning of the enzyme.
The main mechanism of action of V-ATPase A4 inhibitors involves blocking the proton-pumping activity of V-ATPase A4, thereby preventing the acidification of cellular compartments. This disruption of pH regulation can have profound consequences on various cellular processes, including endocytosis, autophagy, and vesicular trafficking. By inhibiting V-ATPase A4, these compounds can perturb intracellular pH levels, leading to alterations in the degradation of cellular waste, the processing of proteins, and the functioning of organelles like lysosomes.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Bafilomycin A1 | 88899-55-2 | sc-201550 sc-201550A sc-201550B sc-201550C | 100 µg 1 mg 5 mg 10 mg | $98.00 $255.00 $765.00 $1457.00 | 280 | |
Binds to the V-ATPase and inhibits the proton pump, preventing acidification of cellular compartments, which is essential for processes like endocytosis and autophagy. | ||||||
Concanamycin A | 80890-47-7 | sc-202111 sc-202111A sc-202111B sc-202111C | 50 µg 200 µg 1 mg 5 mg | $66.00 $167.00 $673.00 $2601.00 | 109 | |
Similar to Bafilomycin A1, it binds to V-ATPase and inhibits proton pumping, interfering with intracellular acidification. | ||||||