Date published: 2026-5-7

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CA VB Inhibitors

The chemical class known as CA VB, or Class A Voltage-gated Calcium Channels (VGCCs), represents a highly specialized group of ion channels that are integral to the process of calcium ion (Ca²⁺) movement across cellular membranes. These channels are pivotal in translating electrical signals into biochemical actions within cells, making them essential components of various physiological processes. CA VB channels are primarily activated by changes in the membrane potential, particularly when the inside of the cell becomes less negative (depolarization). Upon activation, these channels allow the influx of Ca²⁺ into the cell, a process that is tightly regulated by the voltage-dependent opening and closing of the channel. The structure of these channels is complex, typically composed of a large alpha1 subunit, which forms the pore through which calcium ions pass, and several auxiliary subunits (alpha2-delta, beta, and gamma), which modulate the channel's properties, including its kinetics, voltage sensitivity, and trafficking to the membrane. The function of CA VB channels extends beyond simple calcium ion conductance. The influx of Ca²⁺ through these channels serves as a key signal that triggers various intracellular processes, such as neurotransmitter release in neurons, muscle contraction, and gene expression. The specificity and precision of CA VB channel activity are governed by a combination of factors, including the expression patterns of different channel subtypes, post-translational modifications, and interactions with other cellular proteins. These channels are also subject to modulation by various endogenous factors, such as G-proteins, phosphorylation states, and interaction with cellular membranes. The diversity within this class of channels is reflected in the existence of multiple isoforms, each with distinct biophysical properties, tissue distribution, and regulatory mechanisms. This complexity allows for a finely tuned calcium signaling process, which is crucial for maintaining cellular homeostasis and supporting a wide range of physiological functions.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Acetazolamide

59-66-5sc-214461
sc-214461A
sc-214461B
sc-214461C
sc-214461D
sc-214461E
sc-214461F
10 g
25 g
100 g
250 g
500 g
1 kg
2 kg
$81.00
$177.00
$434.00
$541.00
$883.00
$1479.00
$2244.00
1
(1)

Acetazolamide binds to the zinc ion in the active site of carbonic anhydrases, inhibiting its activity.

Methazolamide

554-57-4sc-235615
1 g
$94.00
3
(1)

This sulphonamide analog functions similarly to acetazolamide and inhibits CA by coordinating with the active site zinc.

Topiramate

97240-79-4sc-204350
sc-204350A
10 mg
50 mg
$107.00
$369.00
(1)

Topiramate inhibits carbonic anhydrase activity by binding to the active site and interfering with the hydration of carbon dioxide.

Dorzolamide

120279-96-1sc-337687
1 g
$960.00
2
(0)

This sulfonamide inhibitor specifically interacts with the catalytic site of carbonic anhydrase, inhibiting its action.

Brinzolamide

138890-62-7sc-481649
10 mg
$269.00
(0)

Brinzolamide binds competitively to the active site zinc and inhibits the enzyme.

Sulphanilamide

63-74-1sc-208410
sc-208410A
sc-208410B
100 g
250 g
1 kg
$43.00
$80.00
$250.00
(0)

As a simple sulfonamide, it can bind to carbonic anhydrases and inhibit their action by mimicking the natural substrate.

4,4′-Dithiodimorpholine

103-34-4sc-486751
25 g
$42.00
(0)

A less common carbonic anhydrase inhibitor whose binding mechanism is similar to that of other sulfonamides.

Benzylamine

100-46-9sc-239323
100 ml
$41.00
(0)

This sulfonamide derivative inhibits carbonic anhydrase by binding to the zinc in the active site.

Hydrochlorothiazide

58-93-5sc-207738
sc-207738A
sc-207738B
sc-207738C
sc-207738D
5 g
25 g
50 g
100 g
250 g
$55.00
$240.00
$333.00
$562.00
$988.00
(0)

Although primarily a diuretic, it can inhibit carbonic anhydrase activity through its sulfonamide group.