PME-1 inhibitors encompass a range of compounds that influence the activity of Protein Phosphatase Methylesterase-1, either directly or indirectly, by modulating associated enzymatic pathways. The primary function of PME-1 is to demethylate and inactivate PP2A, a significant phosphatase in cellular signaling. Therefore, inhibitors of PME-1 can indirectly enhance PP2A activity, impacting various cellular processes. The list includes compounds like Sinefungin and adenosine derivatives, which are known to affect methyltransferase activities. These molecules may indirectly influence PME-1 function, as PME-1 is involved in the methylation-demethylation equilibrium of PP2A. Similarly, molecules like Methylthioadenosine and its derivatives could act as competitive inhibitors or influence the methylation status of PP2A.
Compounds such as Fostriecin represent a different approach, where instead of inhibiting PME-1, they activate PP2A. This strategy can counteract the inactivation of PP2A by PME-1. In contrast, chemicals like Cantharidin, Okadaic Acid, and Microcystin-LR are PP2A inhibitors, included in the list to provide a broader perspective on the regulation of PP2A and its associated enzymes. These compounds illustrate the complexity of targeting specific phosphatase pathways and the indirect approaches that might be necessary to modulate enzymes like PME-1.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Sinefungin | 58944-73-3 | sc-203263 sc-203263B sc-203263C sc-203263A | 1 mg 100 mg 1 g 10 mg | $271.00 $5202.00 $40368.00 $704.00 | 4 | |
A nucleoside antibiotic that inhibits protein methyltransferases, potentially affecting PME-1 activity indirectly. | ||||||
Adenosine, periodate oxidized | 34240-05-6 | sc-214510 sc-214510A | 25 mg 100 mg | $119.00 $364.00 | ||
A chemical that can modify adenosine residues and potentially affect PME-1's interaction with its substrates. | ||||||
Homocysteine | 6027-13-0 | sc-507315 | 250 mg | $195.00 | ||
A product of methyltransferase reactions that can act as a methyltransferase inhibitor, potentially influencing PME-1 activity. | ||||||
5′-Deoxy-5′-methylthioadenosine | 2457-80-9 | sc-202427 | 50 mg | $122.00 | 1 | |
A molecule similar in structure to the substrate of PME-1, could potentially act as a competitive inhibitor. | ||||||
Fostriecin | 87860-39-7 | sc-202160 | 50 µg | $265.00 | 9 | |
A PP2A activator, which could counteract the inactivation of PP2A by PME-1. | ||||||
Cantharidin | 56-25-7 | sc-201321 sc-201321A | 25 mg 100 mg | $89.00 $279.00 | 6 | |
A potent inhibitor of PP2A, its inclusion is to demonstrate chemicals that have opposite effects to PME-1 inhibition. | ||||||
Okadaic Acid | 78111-17-8 | sc-3513 sc-3513A sc-3513B | 25 µg 100 µg 1 mg | $291.00 $530.00 $1800.00 | 78 | |
Another PP2A inhibitor, included for contrast to PME-1 inhibitors. | ||||||
Endothall | 145-73-3 | sc-201325 sc-201325A | 20 mg 100 mg | $49.00 $203.00 | 1 | |
An inhibitor of PP2A and PP1, illustrating the complexity of targeting specific phosphatase pathways. | ||||||
Norcantharidin | 29745-04-8 | sc-280719 | 5 g | $113.00 | 2 | |
A derivative of cantharidin with similar PP2A inhibitory activity. | ||||||
Calyculin A | 101932-71-2 | sc-24000 sc-24000A | 10 µg 100 µg | $163.00 $800.00 | 59 | |
A marine natural product that inhibits PP1 and PP2A, showcasing the range of PP2A-targeting compounds. | ||||||