Date published: 2026-4-1

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vacuolar proton pump Inhibitors

Vacuolar proton pump inhibitors are a class of chemical compounds specifically designed to inhibit the activity of vacuolar proton pumps, which are crucial for maintaining the acidic environment within various intracellular compartments such as lysosomes, endosomes, and vacuoles. These proton pumps, often referred to as vacuolar-type H+-ATPases (V-ATPases), play a fundamental role in cellular processes by actively transporting protons (H+) across the membrane of these organelles. This proton transport is essential for creating and sustaining the acidic pH required for enzyme activation, protein degradation, and various other cellular functions.

The mechanism of action of vacuolar proton pump inhibitors involves binding to specific sites on the V-ATPase enzyme complex, thereby obstructing its ability to transport protons. This inhibition results in a decrease in the acidity of the intracellular compartments, which can disrupt the normal function of enzymes and processes that rely on the acidic environment. By studying these inhibitors, researchers aim to gain a deeper understanding of the role of V-ATPases in cellular homeostasis and the impact of their inhibition on cellular processes. This research can reveal how changes in proton pump activity affect intracellular pH regulation, enzyme function, and overall cellular dynamics.

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)

Bafilomycin A1 is a specific inhibitor of the V-ATPase (vacuolar proton pump). It binds to the V0 subunit c, inhibiting proton translocation and ATP hydrolysis, leading to the functional inhibition of the proton pump.

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)

Concanamycin A is another specific inhibitor of V-ATPase. It acts similarly to Bafilomycin A1 by binding to the V0 subunit of the enzyme, inhibiting proton transport and ATPase activity, resulting in inhibition of the vacuolar proton pump's function.

3-Indoleacetic acid

87-51-4sc-254494
sc-254494A
sc-254494B
5 g
25 g
100 g
$31.00
$92.00
$160.00
4
(1)

Indole-3-acetic acid, while primarily known as a plant hormone, has been shown to inhibit V-ATPase activity in plants by disrupting the proton gradient, which suggests that it could inhibit the vacuolar proton pump in a similar fashion.

Piceatannol

10083-24-6sc-200610
sc-200610A
sc-200610B
1 mg
5 mg
25 mg
$51.00
$71.00
$199.00
11
(2)

Piceatannol has been reported to inhibit V-ATPase activity. It interferes with the ATP binding site on the V1 domain of V-ATPase, impeding ATP hydrolysis and subsequently inhibiting the vacuolar proton pump.

Lys05

1391426-24-6sc-507532
5 mg
$140.00
(0)

Lys05 is a dimeric chloroquine derivative that has been shown to inhibit V-ATPase. It accumulates in lysosomes, disrupting their acidic pH by inhibiting the vacuolar proton pump, which is essential for lysosome function.