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.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Phenylarsine oxide | 637-03-6 | sc-3521 | 250 mg | $41.00 | 4 | |
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 | 13721-39-6 | sc-3540 sc-3540B sc-3540A | 5 g 10 g 50 g | $49.00 $57.00 $187.00 | 142 | |
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 | 87860-39-7 | sc-202160 | 50 µg | $265.00 | 9 | |
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 | 78111-17-8 | sc-3513 sc-3513A sc-3513B | 25 µg 100 µg 1 mg | $291.00 $530.00 $1800.00 | 78 | |
A toxin produced by certain marine organisms. Potently inhibits serine/threonine phosphatases such as PP1 and PP2A by binding to their active sites. | ||||||
Cantharidin | 56-25-7 | sc-201321 sc-201321A | 25 mg 100 mg | $89.00 $279.00 | 6 | |
A terpenoid produced by many beetles. Inhibits serine/threonine phosphatases PP1 and PP2A by binding to their active sites. | ||||||
5-Iodotubercidin | 24386-93-4 | sc-3531 sc-3531A | 1 mg 5 mg | $153.00 $464.00 | 20 | |
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 | 101932-71-2 | sc-24000 sc-24000A | 10 µg 100 µg | $163.00 $800.00 | 59 | |
A toxin isolated from marine sponges. Inhibits PP1 and PP2A by binding to their active sites. | ||||||
C-8 Ceramide | 74713-59-0 | sc-205233 sc-205233A sc-205233B | 1 mg 5 mg 25 mg | $19.00 $63.00 $228.00 | 1 | |
A family of lipid molecules. Not direct phosphatase inhibitors. Ceramides can modulate cellular signaling pathways and might affect phosphatase activity in an indirect manner. | ||||||