Date published: 2026-4-1

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V-ATPase A4 Inhibitors

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.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Bafilomycin A1

88899-55-2sc-201550
sc-201550A
sc-201550B
sc-201550C
100 µg
1 mg
5 mg
10 mg
$98.00
$255.00
$765.00
$1457.00
280
(6)

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

80890-47-7sc-202111
sc-202111A
sc-202111B
sc-202111C
50 µg
200 µg
1 mg
5 mg
$66.00
$167.00
$673.00
$2601.00
109
(2)

Similar to Bafilomycin A1, it binds to V-ATPase and inhibits proton pumping, interfering with intracellular acidification.