Date published: 2025-11-1

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V1RH18 Inhibitors

V1RH18 inhibitors represent a specialized class of chemical compounds designed to interact with the V1RH18 protein, which is part of the vacuolar-type H+-ATPase (V-ATPase) complex. This complex is essential for maintaining acidic environments within various intracellular compartments, including lysosomes, endosomes, and vacuoles, by utilizing ATP hydrolysis to pump protons across membranes. V1RH18 is situated in the V1 domain of the V-ATPase and plays a role in the ATP hydrolysis activity crucial for proton pumping. The inhibitors targeting V1RH18 are crafted to bind specifically to this protein, thereby modulating its function and, by extension, the activity of the entire V-ATPase complex.

The primary action of V1RH18 inhibitors involves disrupting the interaction between V1RH18 and other components of the V1 domain. This disruption can impede the ability of V1RH18 to participate in ATP hydrolysis, which is fundamental for the proper function of the V-ATPase complex. As a result, the inhibitors can affect the assembly, stability, and enzymatic activity of the V1 domain, leading to alterations in the proton pump's efficiency. By targeting V1RH18, these compounds provide a tool to investigate the specific contributions of this protein to the overall function of the V-ATPase complex, including its role in intracellular pH regulation and vesicular trafficking. Understanding the impact of V1RH18 inhibition helps to elucidate the broader implications of V1RH18's function within the V-ATPase machinery.

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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Suberoylanilide Hydroxamic Acid

149647-78-9sc-220139
sc-220139A
100 mg
500 mg
$130.00
$270.00
37
(2)

Vorinostat inhibits histone deacetylases, potentially leading to alterations in chromatin structure and repression of V1R212 expression.

Romidepsin

128517-07-7sc-364603
sc-364603A
1 mg
5 mg
$214.00
$622.00
1
(1)

Romidepsin inhibits histone deacetylases, potentially leading to alterations in chromatin structure and repression of V1R212 expression.

MS-275

209783-80-2sc-279455
sc-279455A
sc-279455B
1 mg
5 mg
25 mg
$24.00
$88.00
$208.00
24
(2)

Entinostat inhibits histone deacetylases, potentially leading to alterations in chromatin structure and repression of V1R212 expression.

Panobinostat

404950-80-7sc-208148
10 mg
$196.00
9
(1)

Panobinostat inhibits histone deacetylases, potentially leading to alterations in chromatin structure and repression of V1R212 expression.

Belinostat

414864-00-9sc-269851
sc-269851A
10 mg
100 mg
$153.00
$561.00
(1)

Belinostat inhibits histone deacetylases, potentially leading to alterations in chromatin structure and repression of V1R212 expression.

Trichostatin A

58880-19-6sc-3511
sc-3511A
sc-3511B
sc-3511C
sc-3511D
1 mg
5 mg
10 mg
25 mg
50 mg
$149.00
$470.00
$620.00
$1199.00
$2090.00
33
(3)

Trichostatin A inhibits histone deacetylases, potentially leading to alterations in chromatin structure and repression of V1R212 expression.

Sodium Butyrate

156-54-7sc-202341
sc-202341B
sc-202341A
sc-202341C
250 mg
5 g
25 g
500 g
$30.00
$46.00
$82.00
$218.00
19
(3)

Sodium butyrate inhibits histone deacetylases, potentially leading to alterations in chromatin structure and repression of V1R212 expression.

Valproic Acid

99-66-1sc-213144
10 g
$85.00
9
(1)

Valproic acid inhibits histone deacetylases, potentially leading to alterations in chromatin structure and repression of V1R212 expression.

Scriptaid

287383-59-9sc-202807
sc-202807A
1 mg
5 mg
$63.00
$179.00
11
(2)

Scriptaid inhibits histone deacetylases, potentially leading to alterations in chromatin structure and repression of V1R212 expression.

PCI-24781

783355-60-2sc-364565
sc-364565A
5 mg
50 mg
$182.00
$1330.00
1
(1)

PCI-24781 inhibits histone deacetylases, potentially leading to alterations in chromatin structure and repression of V1R212 expression.