Date published: 2026-4-1

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PAP-2c Inhibitors

PAP-2c inhibitors belong to a unique class of chemical compounds designed to target and inhibit the PAP-2c enzyme, also known as Phosphatidic Acid Phosphatase type 2c. PAP-2c is an enzyme that plays a crucial role in lipid metabolism. Specifically, it is responsible for the dephosphorylation of phosphatidic acid (PA) to produce diacylglycerol (DAG). The structure and function of PAP-2c make it a distinctive target for molecular interventions, and as a result, various compounds have been designed and developed to modulate its activity.

The mechanism of action of PAP-2c inhibitors primarily centers around the binding of the inhibitor to the active site of the PAP-2c enzyme, preventing the enzyme from accessing its natural substrate, phosphatidic acid. This binding effectively hampers the conversion of PA to DAG. The specific interactions between the inhibitor and the enzyme often involve hydrogen bonds, hydrophobic interactions, and sometimes ionic bonds, depending on the structure of the specific inhibitor. The structural design of these inhibitors typically aims at maximizing their affinity for the enzyme while minimizing potential off-target effects. Achieving this balance ensures the specificity of the inhibitor for the PAP-2c enzyme, reducing unintended interactions with other biological molecules or systems.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Phenylarsine oxide

637-03-6sc-3521
250 mg
$41.00
4
(1)

An organoarsenic compound. Binds to vicinal (adjacent) thiol groups, which are common in the active sites of many phosphatases. This binding can disrupt the enzyme's activity.

Sodium Orthovanadate

13721-39-6sc-3540
sc-3540B
sc-3540A
5 g
10 g
50 g
$49.00
$57.00
$187.00
142
(4)

An inorganic salt of vanadic acid. Acts as a transition state analog for the phosphate group. By mimicking the transition state of the enzymatic reaction, it can bind and inhibit phosphatases.

Fostriecin

87860-39-7sc-202160
50 µg
$265.00
9
(1)

A complex organic molecule isolated from bacteria. Known to inhibit serine/threonine phosphatases like PP2A and PP4, likely through binding to their active sites.

Okadaic Acid

78111-17-8sc-3513
sc-3513A
sc-3513B
25 µg
100 µg
1 mg
$291.00
$530.00
$1800.00
78
(4)

A toxin produced by certain marine organisms. Potently inhibits serine/threonine phosphatases such as PP1 and PP2A by binding to their active sites.

Cantharidin

56-25-7sc-201321
sc-201321A
25 mg
100 mg
$89.00
$279.00
6
(1)

A terpenoid produced by many beetles. Inhibits serine/threonine phosphatases PP1 and PP2A by binding to their active sites.

5-Iodotubercidin

24386-93-4sc-3531
sc-3531A
1 mg
5 mg
$153.00
$464.00
20
(2)

A derivative of the nucleoside adenosine. Primarily known as an adenosine kinase inhibitor, but might affect certain phosphatases indirectly through modulation of cellular adenosine levels.

Calyculin A

101932-71-2sc-24000
sc-24000A
10 µg
100 µg
$163.00
$800.00
59
(3)

A toxin isolated from marine sponges. Inhibits PP1 and PP2A by binding to their active sites.

C-8 Ceramide

74713-59-0sc-205233
sc-205233A
sc-205233B
1 mg
5 mg
25 mg
$19.00
$63.00
$228.00
1
(0)

A family of lipid molecules. Not direct phosphatase inhibitors. Ceramides can modulate cellular signaling pathways and might affect phosphatase activity in an indirect manner.